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    <title>Recent Comments on 'Caring Currents' | Caring.com</title>
    <link>http://www.caring.com/blogs/caring-currents</link>
    <language>en-us</language>
    <ttl>60</ttl>
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      <title>Comment on SelfCare: 7 Things To Do When You're Stressed to Wit's End</title>
      <description>Thanks for the suggestions.  I do the breathing, but even though I like tea, I had never thought of using that.  I had an amazing stress reliever yesterday, something I would never have come up with.  I went to a class for work.  My bother was with my mom, but I ususally still worry.  Well, for hours, I concentrated on what I needed to learn and realized that I hadn't had a stomach ache all day!  It was work, but I was totally distracted and it made a huge difference in my day, and in how I slept last night, and how I feel today.  Who'd a thunk it?  :-)</description>
      <author>Wild Mary</author>
      <pubDate>Fri, 06 Nov 2009 16:36:03 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-selfcare-seven-7-things-to-do-when-youre-stressed-to-wits-end</guid>
      <link>http://www.caring.com/blogs/the-selfcare-seven-7-things-to-do-when-youre-stressed-to-wits-end/comments</link>
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      <title>Comment on Cell Phones That Won't Scare Mom</title>
      <description>This was a great article!  Phones and technology in general can be very scary for the elderly.  
But, a cell phone is not always the best thing as it is easy to lose and their is a monthly fee, etc.  Another solution is FotoDialer.  It allows the user to dial phone numbers by photos that are 2x3 inches.  It is for analog land lines and connects to the existing phone, has no monthly fee, and is very intuitive.  FotoDialer holds 24 pictures in its six pages.  The person just finds the photograph of the person/place they want to call and pushes a big black button next to their face and FotoDialer calls that person.  The first page is dedicated to emergency numbers.  http://www.PhotoDialing.com  or  http://www.FotoDialer.com </description>
      <author>JoeE71</author>
      <pubDate>Thu, 05 Nov 2009 23:42:08 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/cell-phones-that-wont-scare-mom</guid>
      <link>http://www.caring.com/blogs/cell-phones-that-wont-scare-mom/comments</link>
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      <title>Comment on Family Financial Feuds: When Mom or Dad Is Gambling Away Financial Security </title>
      <description>Good for you.  I am glad that you were able to handle it on your own.  While I agree that people should be open minded and believe that it CAN be done on their own, I also believe that it is equally as important to be open minded enough to understand that there may be people in the world that aren't like you and can't just do it on their own.  

Everyone is different.  People who can stop on their own DO and those who can't (or think they can't) either continue with their addiction and allow it to destory their life or they get help.  

By the way, if you can &quot;handle&quot; going only a few times a year and only spend &quot;$20&quot; when you do go - maybe your 'problem' was less of a 'problem' than you think.  If it only got out of control and you were able to pull control back in -- it is less likely that you are an addict and more just someone who got out of control who pulled it back in.  

Addiction is a real disease.  If it weren't - insurance wouldn't cover it. 
</description>
      <author>Anonymous</author>
      <pubDate>Thu, 05 Nov 2009 15:13:51 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-financial-feud-2-when-mom-or-dad-is-gambling-financial-security-away</guid>
      <link>http://www.caring.com/blogs/family-financial-feud-2-when-mom-or-dad-is-gambling-financial-security-away/comments</link>
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      <title>Comment on SelfCare: 7 Things To Do When You're Stressed to Wit's End</title>
      <description>Thank you while  I sit hear and crey I will go have that cup of tea, and chocolate to</description>
      <author>cool</author>
      <pubDate>Wed, 04 Nov 2009 16:54:46 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-selfcare-seven-7-things-to-do-when-youre-stressed-to-wits-end</guid>
      <link>http://www.caring.com/blogs/the-selfcare-seven-7-things-to-do-when-youre-stressed-to-wits-end/comments</link>
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      <title>Comment on SelfCare: 7 Things To Do When You're Stressed to Wit's End</title>
      <description>Great article Paula,

Thanks for putting up these stress-relieving strategies. The cup of tea is definitely one that I indulge in on a regular basis. 

I do think that you left one off the list. If you want to buy yourself time to regain a little sanity. I would recommend actually buying a little time. Maybe take a week or two off of caregiving and hire an accredited caregiver for a week or two and just take a vacation from caregiving. Maybe that is a trip or just a long tea break, but stepping away often makes decisions more clear.

For more information on in-home caregivers, check out this blog: www.rightathome.net/seniorhomecare.

Best Wishes,
Bill</description>
      <author>RightatHome</author>
      <pubDate>Mon, 02 Nov 2009 15:05:05 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-selfcare-seven-7-things-to-do-when-youre-stressed-to-wits-end</guid>
      <link>http://www.caring.com/blogs/the-selfcare-seven-7-things-to-do-when-youre-stressed-to-wits-end/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>I took care of my Dad who had been diagnosed with AD. And, although I was in front and center in my career, I knew it was payback time. Right before my dad moved in with me, a dear friend had been going through many troubled times with her husband who also had alzheimers. She shared with me a story that certainly made a huge difference in my abilities to care for my father. She and her husband lived in Northridge. When the huge earthquake hit Northride, their home was hit hard. It hit around 4:00 am. She and her husband awoke to watching their entire bedroom collapse around them as they sat straight in bed holding onto each other. After several moments of watching their precious mementos, lamps, clocks, clothes, chests, tables, chairs, and drawers, falling all around them, my friend looked at her husband. He had a very quizzical look on his face. She wasn't sure how she was going to explain this to him. She found she wouldn't need to. He looked at her after all the noise and commotion, and said, &quot;Now look what you have done!&quot; At that very moment, she knew it was time to laugh. She began laughing, and he began laughing too. She said it brought much comfort in the knowledge, that yes indeed, you must be able to laugh! She vowed, she would always find that time to enjoy laughter with her husband.</description>
      <author>sdprocter</author>
      <pubDate>Sun, 01 Nov 2009 02:11:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>i'm still laughing about hillary and maybe tomorrow</description>
      <author>loveforu</author>
      <pubDate>Sat, 31 Oct 2009 21:47:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>I don't remember!</description>
      <author>Anonymous</author>
      <pubDate>Sat, 31 Oct 2009 18:53:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Family Financial Feuds: When Mom or Dad Is Gambling Away Financial Security </title>
      <description>I understand that gambling can be a huge problem (I was a casual( bingo, keno) gambler for years, caused me many problems. I decided to quit on my own (it is possible)and have never regretted it. I do occasionally go to a local hall, $20 only. When it's gone so am I.I go about 3 times a year. My real reason for writing is why should kids expect something from their parents, that the PARENTS worked hard for, I have seen so many close friends families torn up over what they were entitled to?? after Mom or Dad pass on. Who r these people? Who raised them? Some are real monsters could care less about parent just what's in it for me!</description>
      <author>msmaddog</author>
      <pubDate>Sat, 31 Oct 2009 15:48:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-financial-feud-2-when-mom-or-dad-is-gambling-financial-security-away</guid>
      <link>http://www.caring.com/blogs/family-financial-feud-2-when-mom-or-dad-is-gambling-financial-security-away/comments</link>
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      <title>Comment on Family Financial Feuds: The Case of the &quot;Borrowing&quot; Sibling</title>
      <description>Mother is 87 in good health. Spends 3 to 4 months a year in each of here (3 out of 8) children. 
She accumulated some wealth through the years, saving them by-the-penny. All three brothers are very kind to her, but two out of the three are spenders of their own money and not penny-savers... the 3rd one (myself) is a good money manager and she realize I appreciate the value of the money... she decided to write in her will all of her money to me... All 3 good brothers are financially comfortable and love our mother, but her choice to be biased to only one child (myself) caused lots of trouble... pressuring her to be fare to at least the three of us, whom she spends part of the year their houses, makes her very mad and says  &quot; I spent my life saving my money very carefully, and now they will spend most of it in few months...&quot; should I ignore her will and (god give her long life) when she completes her life... just distribute the money evenly on 3,,, or even on all 8..... dilemma... None of the three need her money... especially me... we are all doing ok..... as a joke you probably saying in your head.. well send the money to me... several &quot;sheakhs&quot; already suggested that....thanks for your advice
joe_zada@yahoo.com  
</description>
      <author>Zada</author>
      <pubDate>Fri, 30 Oct 2009 22:34:50 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-deal-with-financial-freeloaders</guid>
      <link>http://www.caring.com/blogs/how-to-deal-with-financial-freeloaders/comments</link>
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      <title>Comment on Family Financial Feuds: The Case of the &quot;Borrowing&quot; Sibling</title>
      <description>There may be more to the legal picture than has been discussed so far.  In some states, the use of one's position (&quot;loving&quot; relative, trusted son, etc.) to gain influence over how an elder uses money for the benefit of the relative may be a crime, too.  &quot;Undue influence&quot; is part of financial elder abuse.  Sadly, it does happen at the hands of family more often than anyone outside the family.  If the level of &quot;borrowing&quot; or taking or persuading an elder who can't say no has reached the point of financial harm to the elder, it's time to consider reporting this to Adult Protective Services, or equivalent in your community.  This can tear families apart, but the elder's financial welfare has to take priority over any concern about the freeloader's embarrassment or consequences. Some freeloaders bankrupt their elders. Take the &quot;borrowing&quot; and helping one's self to Mom's funds seriously. It can be a violation of the law and financial elder abuse. See an elder law attorney for advice if this is what is happening in your family. Carolyn Rosenblatt, R.N., Attorney, AgingParents.com</description>
      <author>Carolyn  L.  Rosenblatt</author>
      <pubDate>Thu, 29 Oct 2009 19:03:02 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-deal-with-financial-freeloaders</guid>
      <link>http://www.caring.com/blogs/how-to-deal-with-financial-freeloaders/comments</link>
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      <title>Comment on SelfCare: 7 Things To Do When You're Stressed to Wit's End</title>
      <description>Thank you for this important and helpful article.  It's a shame that we all have to be reminded (and remind ourselves) that it's not only OK, but necessary, to take care of ourselves and to sometimes put ourselves first.  No one thing works for everyone, but you offer a wonderful menu of choices.  At www.activeseniorsintransition.com we have found that people in the &quot;sandwich generation&quot; who consider their own needs, have more to give to their children and aging parents.  </description>
      <author>DeborahS</author>
      <pubDate>Thu, 29 Oct 2009 13:56:23 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-selfcare-seven-7-things-to-do-when-youre-stressed-to-wits-end</guid>
      <link>http://www.caring.com/blogs/the-selfcare-seven-7-things-to-do-when-youre-stressed-to-wits-end/comments</link>
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      <title>Comment on Family Financial Feuds: The Case of the &quot;Borrowing&quot; Sibling</title>
      <description>This blog answered a lot of questions for me. You totally described my freeloading sibling. Now I understand his condition I won't stress myself so much. I know what to do now. Thank You..</description>
      <author>Anonymous</author>
      <pubDate>Wed, 28 Oct 2009 23:54:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-deal-with-financial-freeloaders</guid>
      <link>http://www.caring.com/blogs/how-to-deal-with-financial-freeloaders/comments</link>
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      <title>Comment on Beware Red Meat, the New Cancer Risk</title>
      <description>How about Venison? (deer meet hunted in nature).  At our home, we rarely eat beef, but instead use venison that we are able to hunt successfully in Michigan. Is it the way the beef is produced or processed with hormones and chemicals? Or is it just the (red) of the meat.  Venison is browner than red when we process it.</description>
      <author>Kym</author>
      <pubDate>Wed, 28 Oct 2009 14:19:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/newslflash-eating-red-meat-raises-cancer-risk</guid>
      <link>http://www.caring.com/blogs/newslflash-eating-red-meat-raises-cancer-risk/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>I forgot to say that my blog, www.KnowItAlz.com shows the lighter (and sometimes downright FUNNY) side of my caring for my Dad who has Alzheimer's and lives with me in NC.  If you need a laugh, there are 700 funny stories from the past few years.

Thanks for all the HUGS and PRAYERS.  I need them!

Kathy</description>
      <author>kathyNC</author>
      <pubDate>Wed, 28 Oct 2009 14:04:26 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>Thank you all for sharing what feel like affirmations to me...Ginnysheen, I could almost picture being in your home, with all those wonderful details. And I also really like the idea of laura l's client's pesky friend &quot;Mr. Alzheimer's&quot;...!</description>
      <author>Paula Spencer</author>
      <pubDate>Wed, 28 Oct 2009 13:46:40 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>Thank you all for sharing what feel like affirmations to me...Ginnysheen, I could almost picture being in your home, with all those wonderful details. And I also really like the idea of laura l's client's pesky friend &quot;Mr. Alzheimer's&quot;...!</description>
      <author>Paula Spencer</author>
      <pubDate>Wed, 28 Oct 2009 13:45:51 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Alzheimer's Phone Problems: Little Object, Big Headaches</title>
      <description>Have a phone where people can call and you can use a speaker phone.  It helps and allows people to enjoy hearing peoples voices.  Also the special phones with no numbers are greatk like Jitterbug.  All they have to do is push one button, ask a live person for a name, and that operator calls it from a list you have given.  If they can still answer a phone, when the  phone rings, they just open it and talk.  </description>
      <author>Joy Golliver</author>
      <pubDate>Tue, 27 Oct 2009 20:51:23 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alzheimers-phone-problems</guid>
      <link>http://www.caring.com/blogs/alzheimers-phone-problems/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>I try to get my wife to laugh every day.  I don't always succeed but when I do I know she is not sad and disoriented.  I worked with a person years ago who believed that if you could make someone laugh you could make someone think.  Perhaps I can't make my wife think, but it pleases me when she is happy.  Several months ago, my wife asked me, &quot;Where is Roger?&quot; (that's me)  I said, &quot;I'm Roger.&quot;  She replied, &quot;No you're not.  He's much older than you.&quot;  Intellectually I knew there was humor in that exchange.  Emotionally, all I saw was the disease.  I have told friends the story.  They all laughed of course.  And I now can laugh at it too.  But it took repeatedly telling the story to overcome my emotion so I could see it intellectually.  </description>
      <author>rogerlunde</author>
      <pubDate>Tue, 27 Oct 2009 20:49:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>Even off color humor can be funny.  We were watching Animal Planet on TV and they were teaching a dog not to hump peoples legs.  Before I could change channels, one man in the home said, &quot;That is one horny dog!&quot;  Now you have to laugh at that!  

Another resident where my husband is living now is &quot;working&quot; on a new business idea called House of Joy, for men.  She keeps recruting the dining staff.  She is serious, but later out of her earing, we all get a kick out of it.</description>
      <author>Joy Golliver</author>
      <pubDate>Tue, 27 Oct 2009 20:44:41 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Beware an Unexpected Source of Caregiver Stress</title>
      <description>I love the way this thread has developed.  All the regrets seem to come from being task focused.  All the solutions come from being in the moment and asking what matters right now.  I love Joy's comment &quot;I choose to give my husband my best every day...&quot;  If we can just put a little space between what we think needs to get done and doing it, a little space between what springs to our lips and what we actually say...how might things be better?  And when we don't put in that space because we are tired or stressed that we forgive ourselves and move forward.
Janice Wallace, The Eldercare Coach
www.caringforcaregivers.com</description>
      <author>Eldercoach</author>
      <pubDate>Tue, 27 Oct 2009 16:38:51 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/beware-an-unexpected-source-of-caregiver-stress</guid>
      <link>http://www.caring.com/blogs/beware-an-unexpected-source-of-caregiver-stress/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>Anonymous with hearing impaired issue: THAT IS ONE OF THE WORST! Both my parents live with my husband and me, and we have to practically yell all the time. And of course, the television is on super-volume. My particular favorite is the afternoon opera session--sure hope the neighbors enjoy it. Both my husband and I have started to realize that we keep doing the &quot;loud thing&quot; even after we leave the house. We were in a restaurant the other night, and a guy came over from THREE tables away and said, &quot;Please don't think I was eavesdropping, but I happened to overhear you mention . . .&quot; We're still laughing about that one. Just grateful we weren't saying anything nasty at the time!</description>
      <author>ginnysheen</author>
      <pubDate>Tue, 27 Oct 2009 16:26:06 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Beware an Unexpected Source of Caregiver Stress</title>
      <description>This one really struck home! I tended, for a long time, to do my &quot;chores&quot; and then spend most of my time in another part of the house, leaving my parents alone with each other (as they have been married 60 years, they really don't want that much &quot;alone time.&quot;) Recently, I've started to sit down in the kitchen before dinner prep with a glass of wine. When either of them passes through, I offer them a drink (coffee, wine, whatever) and ask them to sit and join me. Not for nothing do they call it &quot;attitude adjustment hour.&quot; It has changed the way I feel about all of this enormously. I'm more than a caregiver--I'm a daughter. They are my parents. This is time I will never regain if I don't take it now. Phew! Saved by premature regret!</description>
      <author>ginnysheen</author>
      <pubDate>Tue, 27 Oct 2009 15:59:42 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/beware-an-unexpected-source-of-caregiver-stress</guid>
      <link>http://www.caring.com/blogs/beware-an-unexpected-source-of-caregiver-stress/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>Just saw all my typos. Sorry! Promise not to repost, lmao!</description>
      <author>ginnysheen</author>
      <pubDate>Tue, 27 Oct 2009 15:21:49 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>My mom has Alzheimer's, and sometimes the only way my brothers, sister and I can deal with it is to laugh about it. She lives on her own in an apartment with all of us taking turns on coming in twice a day, but it falls the hardest on my oldest brother. He takes care of all the doctor's appointments, gets the scripts, organizes them and makes a list with times and doses so the rest of us give her the right things at the right times, etc. The rest of us take over different aspects of her care, but he's her executor and his name is also on her checks. He's always been the most responsible one (he's the oldest of us six), and he's under such stress that he's been damaging his teeth, grinding them so hard some have cracked. Sometimes, I think the only relief he's got from watching Mom slowly disappear and be replaced with a sometimes mean, hurtful stranger is to talk with others of us on the phone and laugh (painfully, but laugh) about the things that happen. Laughter IS the best medicine; sometimes it's either laugh or cry, and if you cry all the time you can't see what you need to do! We NEED to laugh, not at the person, but at the situation, or we will go mad. Don't worry about what others outside think; do what keeps you sane. If your loved ones could be themselves again, they'd probably laugh about a lot of the stuff too. God bless us all.</description>
      <author>beatbreastcancer</author>
      <pubDate>Tue, 27 Oct 2009 15:17:55 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>This will probably be too long a post, but it's a subject dear to my heart--can't help it. My father is 90, sharp as a tack, but with cardiac problems, and mother 80 with AD, and not a physical problem to speak of--ironic, no? I have eight siblings, half nearby, and half 500 miles away, so lots of phone and email reporting makes laughing over the situation here routine. My family has always been close, regardless of the occasional and inevitable sibling rivalry, but the family sense of humor has always been outrageous, and others often find it appalling when we are howl over something--especially things others don't even discuss. Without laughing at the crazy things, Id be crazier than I am now! My mother, particularly on her better days, still cracks up with the rest of us, even when the joke invloves one of her &quot;adventures&quot;. She loves to walk, and the first time she lost her way, she sat down on a corner and teased about her &quot;hitchhiking&quot; ever since, and she looks up at that, shrugs, and tells us that &quot;he was a very nice man.&quot; And it was starting to rain!&quot; One day she put the kettle on to boil for tea, and couldn't figure out why it wouldn't. &quot;Um . . . probably because you put it on the knob instead of the burner?&quot; She said, realizing her error, &quot;I did it intentionally to see if it would boil from there. Guess not.&quot; Then she cracked up and said. &quot;[Expletive deleted], at least now I can blame all this on the Alzheimer's.&quot; My parents both live with me, so this is constant. There's always something silly to laugh about. I ask &quot;Do you remember being queen of the prom?&quot; She says &quot;Really? Was I?&quot; I say &quot;no--see? Your memory is not that bad at all!&quot; She was always a lady as we were growing up, and quite offended when any of us swore or were &quot;vulgar&quot;. No more. Now her favorite chore is to load the dishwasher. The five minute job takes her an hour or two, and she swears away the entire time.We laugh when we try to find something in the kitchen, and they are, well . . . just not there. My husband will tell her &quot;treasure hunt time, Mom&quot; and she laughs with him when they find serving bowls in her bedroom closet. She likes to put away her and my father's laundry, but only recognizes her underwear as her own. She doesn't recognize her clothing, brings it to me and says &quot;this must be yours.&quot; I say thanks, and that I really like wearing things two sizes too large.&quot; We all howl at how often she thanks us for buying new clothes for her. When she has a second glass of wine as we cringe and pray that the rugs will give up the stains, we tell her she should be drinking white, not red! Every time I forget something myself in a standard semi-senior moment, she looks at me, laughs, and tells me that this is divine retribution, and her chance to get even. At a family gathering when sibs were visiting, she, who always said &quot;urination&quot; and &quot;bowel movement&quot; walked into the room and asked if someone would give her a hand because &quot;I have just PISSED all over my pants.&quot; We all laughed and yelled &quot;hell no!&quot; She stared us down, and said &quot;I raised you all; that's gratitude for you!&quot; Of course she got the assistance, but it was one of those things where we all laughed together. I took her to change her clothes, and she got weepy. To console her, I said that it even happens to me, so she should just forget about. She said &quot;well, no problem with that, is there?&quot; Then she asked if it really happened to me, and I told her &quot;hell, no! I was just trying to make you feel better.&quot; Then we sat there on the bed and laughed til we both cried--the good kind of crying. Sometimes it's funny, often it's not. My father is pushing sainthood for his good humor and patience, but even he will get really silly with her. He'll tell her he always assumed he'd go first, and now wishes he had, look up to the ceiling, roll his eyes, and holler &quot;Take me now!&quot; She fires back &quot;No such luck.&quot; I get a good deal of relief from nearby sibs, and even the out-of-towners come often to stay for a few days and &quot;run the show.&quot; When she asks why one of her kids hasn't called in weeks (and they really haven't) we just tell her she spoke with them the night before. Every meal is one she's never had before. What is this? The weekly meatloaf or spaghetti. &quot;Fabulous--you should make this again sometime.&quot; We discuss the whole thing with her often (no choice--she won't remember the prior conversations), and have explained to her how AD affects the brain at least a thousand times. EVERY time, she says, straightfaced, &quot;thank heavens it doesn't affect my mind.&quot; Then she looks over her shoulder and says &quot;It's Alzheimer's you dope! I thought you knew about this kind of thing&quot;. And smirks. Her bad times can be very bad--almost intolerable--but knowing that ANYTHING can be funny when we need it to be. It makes a day so much better. My father loves to tell about her confusing her underwear and trying to pull a bra over her legs, at which time she asked in annoyance, doesn't anyone know how to make underear any more?

My sweet, loving, helpful sister-in-law's mother, who also had AD, died recently--not funny at all. While we were in their home after the wake, my mother stage-whispered to me &quot;She's better off--she had Alzheimer's, you know.&quot; It got very quiet for a moment, and then we ALL broke up. We have a sense of when things will be upsetting to her, and then we laugh among ourselves out of her earshot; pretty easy, as she's also hard of hearing. But . . . Ya gotta laugh! There will be lots of time to cry later, when she's gone and this is all retrospective. But twenty bucks says we'll be laughing again in minutes, and she wouldn't have wanted it to be any other way. </description>
      <author>ginnysheen</author>
      <pubDate>Tue, 27 Oct 2009 15:15:48 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>As co-leader of an Alzheimer's support group, I met a bright spirited woman who would report on the latest glitches caused by her pestiferous friend &quot;Mr. Alzheimer&quot; --I think this gave her some feeling of control over her situation.</description>
      <author>laura liddell</author>
      <pubDate>Tue, 27 Oct 2009 14:23:20 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>My name is Kathy and I am the full time caregiver for my eighty one year-old Dad who has Alzheimer's and lives with me in North Carolina.

When my Mom died in 2004 and Dad moved in with me, I had no idea what to do.  But day by day, I found ways to cope, and even enjoy having my Dad with me.

I feel that laughter is the only thing that is keeping me sane!

Please pass this link along to anyone you feel would enjoy it. www.KnowItAlz.com

Thanks!
Kathy Hatfield

</description>
      <author>kathyNC</author>
      <pubDate>Tue, 27 Oct 2009 13:05:19 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Is It Ever Okay to Laugh About Alzheimer's? </title>
      <description>Thank you for permission to laugh!  I always make jokes in stressful situations, and with Mom's dementia, I am often thought disrespectful or morose.  My Dad has the patience of a saint, God Bless him, and he and I share giggles and guffaws over some of Mom's behaviors, accusations and distorted memories.  He has been accused of not loving her or making fun of her, but that is far from the truth. It is very hard to lose a loved one when they are standing right in front of you.  Laughter helps to ease some of the pain of that loss.  Thank you again for permission to laugh.</description>
      <author>Kristarr</author>
      <pubDate>Tue, 27 Oct 2009 12:09:49 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-ever-okay-to-laugh-about-alzheimers</guid>
      <link>http://www.caring.com/blogs/is-it-ever-okay-to-laugh-about-alzheimers/comments</link>
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      <title>Comment on Beware an Unexpected Source of Caregiver Stress</title>
      <description>I love the comment &quot;...regrets are forever.  I am currently in my living space i.e. my bedroom while my Mom is in the living room watching T.V.  I can't stand the TV being so loud so I disappear.  Ya know after reading this, the reason I'm here is caring for my Mom and that means more then cooking and cleaning.  Thank you so much for the reminder, I think I will go and watch TV with my Mom.  I think lonliness is the worst illness and so easy to cure.  Thanks again.

Imelda</description>
      <author>imelda</author>
      <pubDate>Mon, 26 Oct 2009 04:54:57 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/beware-an-unexpected-source-of-caregiver-stress</guid>
      <link>http://www.caring.com/blogs/beware-an-unexpected-source-of-caregiver-stress/comments</link>
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      <title>Comment on Beware an Unexpected Source of Caregiver Stress</title>
      <description>Thx for the feedback...helpful to hear that everybody has some kind of regret or another...</description>
      <author>Carol O'Dell</author>
      <pubDate>Mon, 26 Oct 2009 00:26:55 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/beware-an-unexpected-source-of-caregiver-stress</guid>
      <link>http://www.caring.com/blogs/beware-an-unexpected-source-of-caregiver-stress/comments</link>
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      <title>Comment on Beware an Unexpected Source of Caregiver Stress</title>
      <description>I recently quit a very part time job as I realized that it was making me short tempered with mom because that was the time she most needed me to be around.  I don't regret it.  Sure I won't have that extra money for a few years but I only have mom for a few more years.  That living in the moment is good advice and try to stress less and smile more...No matter how much time you have with your loved one, regret is forever.  This website is a godsend.  It helps you to keep things in perspective.  Thanks Caring.com</description>
      <author>PT Cruzr</author>
      <pubDate>Sat, 24 Oct 2009 16:05:55 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/beware-an-unexpected-source-of-caregiver-stress</guid>
      <link>http://www.caring.com/blogs/beware-an-unexpected-source-of-caregiver-stress/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>Including other family members in the decision making is waht stress's me the most.  I have POA,  but try to get the opinons of everyone involved in caring for our Mother.  Its not always easy and never pleasant!  For instance --- I may have to move our Mother from the facility she's in now,  to an Alzheimer's Lock-down facility.  Some think its a great place.  Some want to take Mother home with them (even though they're not capable of taking care of themselves),  and some want to move her to a different facility!  I get hate mail and siblings hanging up on me!  There is no happiness.  I just want to do what I feel is best for our Mom.  It shouldn't be so hard!  </description>
      <author>Anonymous</author>
      <pubDate>Sat, 24 Oct 2009 01:26:40 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Swine Flu Deaths: Keeping Sane and Safe</title>
      <description>Melanie, I really appreciate your coverage of the H1N1 vaccine. Truly, the knowledge your spreading here did make me worry less.

It's so rare to find reporting on H1N1 that doesn't deal in hysteria or a desire to grab readers. 

I really thank you for clearly stating the high-risk categories and what to do about getting access to the vaccine.</description>
      <author>Anonymous</author>
      <pubDate>Fri, 23 Oct 2009 19:52:27 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/swine-flu-deaths</guid>
      <link>http://www.caring.com/blogs/swine-flu-deaths/comments</link>
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      <title>Comment on Beware an Unexpected Source of Caregiver Stress</title>
      <description>Regrets, Paula you certainly picked some big ones for your post.  Another one for me is being distracted.  Caregiving brings so many tasks, I think we can forget to slow down and appreciate the person we are caring for.  While recently helping an elderly friend I found myself making a conscious choice to slow down.  I could have been all caught up in rushing around and trying to get her to move faster but that would have just caused more stress.  Being in the moment with her and moving a more of her pace made our time together better.
Janice Wallace, The Eldercare Coach
www.caringforcaregivers.com</description>
      <author>Eldercoach</author>
      <pubDate>Fri, 23 Oct 2009 18:03:27 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/beware-an-unexpected-source-of-caregiver-stress</guid>
      <link>http://www.caring.com/blogs/beware-an-unexpected-source-of-caregiver-stress/comments</link>
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      <title>Comment on Beware an Unexpected Source of Caregiver Stress</title>
      <description>Great article.  My husband is in skilled nursing/hospice, and I see so many other families arguing over little things that don't make any difference. Saying harsh things out of stress.  I know that after the fact, they will feel guilt because they did not show all the love they could have.  I even have patients say to me, how can you keep smiling so much?  My answer, we all have choices and I choose to give my husband my best every day. In other words, I am trying to live my life as it is happening right now, so I don't have any regrets later.  It is a choice and not always easy.</description>
      <author>Joy Golliver</author>
      <pubDate>Fri, 23 Oct 2009 14:44:22 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/beware-an-unexpected-source-of-caregiver-stress</guid>
      <link>http://www.caring.com/blogs/beware-an-unexpected-source-of-caregiver-stress/comments</link>
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      <title>Comment on How Family Caregiving Can Save You Money on Your Taxes</title>
      <description>That would be good to know.  I'm caring for my husband, age 53 (early onset) and I am 52. Hope all is well with you :)</description>
      <author>JoyceT</author>
      <pubDate>Fri, 23 Oct 2009 00:33:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/save-on-tax-if-a-caregiver</guid>
      <link>http://www.caring.com/blogs/save-on-tax-if-a-caregiver/comments</link>
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      <title>Comment on Forgetting Faces: What It's Like to No Longer Be Recognized by Your Dad</title>
      <description>I never ever thought my mother could fail to recognize me, her beloved elder daughter, so when it first happened I was incredulous. That was years ago. I've totally adjusted. I don 't usually bother telling her who I am because she'll forget it a moment later. And there have been times when she just didn't believe me, anyway, and said she didn't have a daughter. Anyway, she doesn't seem to care who I am as long as I'm smiling at her. And now I'm totally fine with that. You can get used to anything, it seems. Now if my father, who's starting to have dementia, stops recognizing me, I don't know how I'll feel...</description>
      <author>Anonymous</author>
      <pubDate>Thu, 22 Oct 2009 21:06:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/forgetting-faces-what-its-like-to-no-longer-be-recognized-by-your-dad</guid>
      <link>http://www.caring.com/blogs/forgetting-faces-what-its-like-to-no-longer-be-recognized-by-your-dad/comments</link>
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      <title>Comment on Beware an Unexpected Source of Caregiver Stress</title>
      <description>Great post Paula,

What can I say? You are right on, we are often so serious about health that we forget about quality of life for the person we are caring for and for ourselves. 

I really liked the part that you wrote about small indulgences. I think that you have to let loved ones enjoy themselves and de-stress yourself. Every caregiver should take some time off and recharge by doing things that they love. Especially with the amount of quality in-home care services out there today.

Great article,

Bill
My Blog: www.rightathome.net/seniorhomecare</description>
      <author>RightatHome</author>
      <pubDate>Thu, 22 Oct 2009 13:55:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/beware-an-unexpected-source-of-caregiver-stress</guid>
      <link>http://www.caring.com/blogs/beware-an-unexpected-source-of-caregiver-stress/comments</link>
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      <title>Comment on Alzheimer's Phone Problems: Little Object, Big Headaches</title>
      <description>My 80 yr old mother has a problem with the modern cordless phones. She doesn't know how to turn the phone on or off. I found an old type of phone with the cord.One that works when you take it off the cradle and turns off when put it back in the cradle. Remember those? LOL It also comes with a couple of cordless that can be put in my bedroom and office. She's not afraid to answer the phone any more, thank gawd. Cause I like checking on her when I have to be gone.</description>
      <author>SheBuddy</author>
      <pubDate>Thu, 22 Oct 2009 06:59:17 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alzheimers-phone-problems</guid>
      <link>http://www.caring.com/blogs/alzheimers-phone-problems/comments</link>
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      <title>Comment on Forgetting Faces: What It's Like to No Longer Be Recognized by Your Dad</title>
      <description></description>
      <author>skampz2</author>
      <pubDate>Thu, 22 Oct 2009 03:51:46 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/forgetting-faces-what-its-like-to-no-longer-be-recognized-by-your-dad</guid>
      <link>http://www.caring.com/blogs/forgetting-faces-what-its-like-to-no-longer-be-recognized-by-your-dad/comments</link>
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      <title>Comment on Forgetting Faces: What It's Like to No Longer Be Recognized by Your Dad</title>
      <description>The first time my mother didn't recognize me, I told her she was my mother and that I was her daughter. The puzzled look in her face made me realized she caught her moment of confusion. We embraced and both cried. Now we I visit, I just announce, Hi mom, it's Kathy. On days that she is more confused...i just let it pass. It alleviates additional stress and confusion for her. </description>
      <author>skampz2</author>
      <pubDate>Thu, 22 Oct 2009 03:51:17 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/forgetting-faces-what-its-like-to-no-longer-be-recognized-by-your-dad</guid>
      <link>http://www.caring.com/blogs/forgetting-faces-what-its-like-to-no-longer-be-recognized-by-your-dad/comments</link>
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      <title>Comment on How Family Caregiving Can Save You Money on Your Taxes</title>
      <description>Would this tax break help me if I am caring for my husband with Alzheimers.  He is 75 and I am 63?</description>
      <author>houcyn</author>
      <pubDate>Wed, 21 Oct 2009 13:22:28 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/save-on-tax-if-a-caregiver</guid>
      <link>http://www.caring.com/blogs/save-on-tax-if-a-caregiver/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>My mother is 89 years old.  She has lived with me in some fashion (my apartment when I was single) with my husband and me for the past 9 years.)  I have taken care of her through a broken shoulder, two broken hips (separate times) and two broken wrists (broken at the same time).  She has osteoporsis.  She was diagnosed with breast cancer at 85 (came through like a trooper); developed congestive heart failure at 86 (she started to slow down a little, but was still able to get around) and she had a stroke this past spring.  This stroke has left my mom pretty much wheelchair bound (she can walk small distances) and she has developed dementia.  My living room is now her bedroom with a wheelchair, walker, potty chair and bed taking up residence. This is the hardest thing I have ever done and I know I am suffering from burnout and am distressed. I have never really had a life of my own without worrying in some fashion about my mom and now I pretty much have no life.  My husband tries to get me out for a few hours on the weekends we have an aide but sometimes it is just too much work to try to figure out how to have &quot;fun&quot; in  hours... I am just worn out I guess... Thanks for listening.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 20 Oct 2009 20:20:27 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on So Your Parent Wants to Move In With You -- Can You Afford It?</title>
      <description>I am lucky to have a 94 year old father with all of his facilities.  Having him live with us for the last ten years has taught my children the importance of family, tolerance and kindness.  It hasn't been easy, the bulk of the care and time is on me.  My sibs do not share the weight and it is causing some stress in my marriage.  Make sure the the primary care giver is appreciated! do something extra to support that person.  Realize that the sib needs a break even if it is not convenient for you.</description>
      <author>ann54</author>
      <pubDate>Mon, 19 Oct 2009 22:40:02 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/parents-moving-in-with-you</guid>
      <link>http://www.caring.com/blogs/parents-moving-in-with-you/comments</link>
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      <title>Comment on 10 Signs of Caring Too Much</title>
      <description>With the huge influx of aging Americans, caregiver burnout is a real problem. I would recommend taking some time off caregiving. Maybe hire an in-home care assistant for the short term to help.

I work on a blog that discusses this topic and and more on aging. Check out www.rightathome.net/seniorhomecare if you are interested.

Keep up the great posts,
Bill</description>
      <author>RightatHome</author>
      <pubDate>Mon, 19 Oct 2009 16:10:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caring-too-much</guid>
      <link>http://www.caring.com/blogs/caring-too-much/comments</link>
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      <title>Comment on Top 10 Breast Cancer Prevention Tips</title>
      <description>Here's a fascinating podcast on the very subject...
http://www.democracynow.org/2009/10/13/author_barbara_ehrenreich_on_bright_sided</description>
      <author>58744152005</author>
      <pubDate>Sat, 17 Oct 2009 21:55:49 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/preventing-breast-cancer</guid>
      <link>http://www.caring.com/blogs/preventing-breast-cancer/comments</link>
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      <title>Comment on Top 10 Breast Cancer Prevention Tips</title>
      <description>i want to take issue with your point 3. your accuracy data on mammography is incorrect (it is much more reliable than indicated), and mri and/or sonograms are only indicated when a mammogram is inclusive. virtually no insurers will pay for a mri or sonogram unless specifically indicated by family history or an inconclusive mammography report. </description>
      <author>rbt</author>
      <pubDate>Sat, 17 Oct 2009 20:36:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/preventing-breast-cancer</guid>
      <link>http://www.caring.com/blogs/preventing-breast-cancer/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>My pet peeves:

&gt;Having to go through endless voicemail hell and long holds to talk to my parents' doctor's advice nurse--and I never ever get to talk to the doctor.
&gt;Having Dad call me all the time, even at 1 a.m., for no special reason, and sometimes leaving voicemail messages marked &quot;urgent.&quot;
&gt;My parents' horrendously overheated house.
&gt;Two completely deaf parents! Even a hearing-enhanced phone doesn't help.
&gt;Dealing with establishing power of attorney agency by agency, bank by bank, etc.--what a bureaucratic nightmare. Worst of the worst: Medicare. No, the V.A.
&gt;Trying to figure out how to help a person read a book if he can't even sit up in bed, can't manage the weight of a book or book-holding device on his chest or stomach, can't see the print if the book's too far away... 
</description>
      <author>Anonymous</author>
      <pubDate>Sat, 17 Oct 2009 20:03:13 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description></description>
      <author>Sister</author>
      <pubDate>Sat, 17 Oct 2009 19:53:56 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>Magster, 
  Just thank goodness we don't live together! Can you imagine the concert we would be subject to everyday! I would punch my eardrums out!</description>
      <author>sop832</author>
      <pubDate>Sat, 17 Oct 2009 16:56:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description></description>
      <author>sop832</author>
      <pubDate>Sat, 17 Oct 2009 16:52:17 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>I guess I never realized how selfish my mom is and always has been though it's gotten worse.  My mom lives with me and all I ask from her is $400 per month to help pay for her care.  I pay for everything except her expensive creams and oils that I couldn't afford but she gets to have.  That's okay but don't make me beg each month for that money.  Lately it seems she's decided I am stealing from her and though I should have seen this coming as she has claimed my sister and 2 of my nieces have stolen from her, it hurts deeply.  
Though this sounds silly, my biggest pet peeve?  She whistles and sings constantly and there's no tune.  It makes me nuts...I have asked her to, &quot;stop whistlin or get a tune&quot;.  As soon as the words come out I feel so bad...I try to remember how fortunate I am to have her with me.  I try! </description>
      <author>Magster</author>
      <pubDate>Sat, 17 Oct 2009 16:13:26 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>It frustrates me that my mother doesn't want to be clean.  I can only get her to take a shower once a week and that is always a hassle because she doesn't want one.  She also doesn't want me to wash her clothes.  She would wear the same thing forever if I didn't take them and wash them.  My mother is 89 and lives with me for almost 5 years, now.  She has some dementia and COPD.  </description>
      <author>Pr0sperity</author>
      <pubDate>Sat, 17 Oct 2009 14:54:42 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>My mom is 95, no memory loss or dementia,just frail and needs help with ADLs. She has an extremely annoying habit of what I call &quot;moaning and groaning&quot; little noises and wheezes that sound like she's in pain or short of breath. She's not even aware of doing it, if I ask what's wrong, she says &quot;Nothing&quot; It annoys me so much, I have to clench my hands and teeth to keep from screaming at her &quot;Stop making those stupid noises!!&quot; </description>
      <author>sop832</author>
      <pubDate>Sat, 17 Oct 2009 14:09:34 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Prevent Diabetes By Treating It Before It Starts</title>
      <description>Thank you for the great information in your article. I really enjoyed reading it. I like to learn what I can about diabetes, I recently found a site that has great information just like yours at www.defeatdiabetesnow.com. Thank you once again.</description>
      <author>Sue K</author>
      <pubDate>Sat, 17 Oct 2009 04:57:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pre-diabetes-treatment</guid>
      <link>http://www.caring.com/blogs/pre-diabetes-treatment/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>I find it poignant that you can comment about your mother sharing, laughing, crying...My mother's affect is so flat that one of the first things I noticed when I came to care for her in June (four months ago) was that now she no longer smiles or laughs, does not care about conversations going on around her (at least she never participates in conversations)and seems to care more about taking her many medications four times a day than eating anything I have prepared.  If it weren't for my father here to help, she would have stopped eating entirely two months ago.
</description>
      <author>XXa</author>
      <pubDate>Fri, 16 Oct 2009 22:51:50 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>SoonerJohn: Your 1st peeve brings up a great &amp; complicated topic, and as for your 2nd -- no, not selfish! See a later post I just wrote on that topic. Everybody deserves solo time. But yes, finding it is the pickle. She sounds lucky to have you.</description>
      <author>Paula Spencer</author>
      <pubDate>Fri, 16 Oct 2009 15:29:04 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>Great listing of pet peeves.  One that is not listed is the lack of appreciation for the huge amount of work being a caregiver is, even when the person being cared for does not live with the caregiver.</description>
      <author>CA-Claire</author>
      <pubDate>Fri, 16 Oct 2009 14:53:58 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>You are right in that every caregiver's role is somewhat different. I am the caregiver for my wife. I have two peeves, at the moment :-), one is that my wife has not yet acknowledged that I am her caregiver, and 2nd is that I have very little time for myself. The latter sounds selfish but it is true. Actually I am fortunate in that her mind is still there. She just cannot walk or get completely dressed by herself. We are very lucky that I am retired and have the time for her. Things could be a great deal worse and I know it.</description>
      <author>SoonerJohn</author>
      <pubDate>Fri, 16 Oct 2009 14:45:58 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>My mom's squeaky wheelchair, how do you oil sealed bearings?</description>
      <author>CHICA60</author>
      <pubDate>Fri, 16 Oct 2009 13:30:24 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on So Your Parent Wants to Move In With You -- Can You Afford It?</title>
      <description>Sue,
Take the time now to locate appropriate care facilities including independent living. You are sooo right if mom is already becomming demanding it will worsen when she has unlimited access. This could also damage your new marrage. First talk to your husband. Be sure that you have his unwavering support. Remind the siblings that you too are now married and in the same boat they are. You are not being selfish you're being sensible. You might consider asking how their respective spouses would have felt newly into a marrage to be facing this. Since she has some financial independence, it makes sense to look now into good continuing care for when the time comes.</description>
      <author>An Hour 4 Me</author>
      <pubDate>Thu, 15 Oct 2009 19:42:14 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/parents-moving-in-with-you</guid>
      <link>http://www.caring.com/blogs/parents-moving-in-with-you/comments</link>
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      <title>Comment on So Your Parent Wants to Move In With You -- Can You Afford It?</title>
      <description>Wow - I have been so blessed with a wonderful family.  Last March when we moved our parents to the city that I live in (pretty much against their will), I had not really thought about any of the things talked about in this article and these comments.  We moved them to a VERY nice Independent Living facility, which also has an Assisted Living area that they can move to if needed.  My siblings all pulled together, and we each helped in the way that best suited our talents and our individual relationship with our parents.  I, the youngest of 4, took care of the medical care and collecting medical records, choosing the facility, chose new medical providers, and assisted with the packing/moving of their home of 34 years - my speciality with that was keeping track of what was sentimental, and what was just 'stuff';  My sister (oldest) coordinated the movers, and assisted with hospital 'sitting' when Dad was in for a week and had hospital psychosis (I took the owl shift (10pm - 7am and made sure I was present when Dr or Nurse Practitioners were there), and kept track of the moving expenses, plus coordinated what we needed our two brothers to help with.  The brothers helped with keeping Mom and Dad up at their 'new' place while the old place was packed up and moved, and provided some support during the move as well.  Now, one brother that lives 40 miles away comes once a week to have dinner with them (even after a full days work), I see them frequently during the week, and my sister and other brother visit approximately quarterly and for special occaisions.  

When my husband passed away recently (I had been his caregiver, and worked full time), my siblings all pulled together and helped with Mom and Dad for the first week, so that I could have time to take care of those things that have to be done post unexpected death.  My siblings helped me enormously with Mom/Dad care and with helping me around my home to make sure that I was OK.

We have talked about the amount of time I have to spend taking care of Mom/Dad, and they are working out a plan to have me paid a monthly stipend from them for the things I do.  It's wonderful to be so well watched out for, when for most of my life, I felt that I was the annoying little sister.

Thanks for listening.</description>
      <author>CA-Claire</author>
      <pubDate>Thu, 15 Oct 2009 15:40:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/parents-moving-in-with-you</guid>
      <link>http://www.caring.com/blogs/parents-moving-in-with-you/comments</link>
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      <title>Comment on So Your Parent Wants to Move In With You -- Can You Afford It?</title>
      <description>Great post Melanie,

That is kind of a sad situation that your friend is in. Sorry to hear it. I have to agree with you though, that defining better ways to fund eldercare is the way it has to be. I agree with #6 get some outside care help because everyone needs days off of caring to just relax.

I work on an eldercare blog that discusses these issues and we are currently writing a series of &quot;paying for eldercare&quot; stories. Check them out at http://www.rightathome.net/seniorhomecare.

Best of luck to your friend,
Bill</description>
      <author>RightatHome</author>
      <pubDate>Thu, 15 Oct 2009 15:38:49 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/parents-moving-in-with-you</guid>
      <link>http://www.caring.com/blogs/parents-moving-in-with-you/comments</link>
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      <title>Comment on So Your Parent Wants to Move In With You -- Can You Afford It?</title>
      <description>Oh, boy. This is a volatile topic for me. I am trying to plan ahead; My elderly mother wants to move in with my new husband and me because she is widowed and lonely. Her personality has slowly changed to be whiny and demanding. She wants to be waited on, either because of her heart (pacemaker) or her diabetes (Type 2). Her health is not so bad that she needs assistance but hints that will be the case soon. 
She can afford to pay her own way but my new husband is aghast and appalled. This was not what he was expecting. I can't really blame him but this puts me in a bad position, and to be truthful I am dreading the possibility.  We don't have a separate living area so she would be right in the middle of everything. My siblings think I am the logical choice because neither of them have room in their houses, and before I married, I took care of Dad who was a stroke victim. (And, years ago, my former husband, who was a cancer victim.)

When I go back and review what I've just written, it sounds selfish and not so bad but I know this will escalate soon and I will have a crisis on my hands. Any advice?</description>
      <author>SueD</author>
      <pubDate>Thu, 15 Oct 2009 14:33:13 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/parents-moving-in-with-you</guid>
      <link>http://www.caring.com/blogs/parents-moving-in-with-you/comments</link>
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      <title>Comment on So Your Parent Wants to Move In With You -- Can You Afford It?</title>
      <description>How about sending the absentee siblings a bill? Use the above system to determine where things are at and when the siblings refuse to participate, send them a bill. Firstly will raise ire in a hurry then while you have their attention secure commitments real ones with actual working drop dead dates failur on their part means thy have nothing to say about her care. NOTHING. If needed you arrange to deal with financial matters yes all of them and make judgements with her doctors/attorneys to get her the best possible care without it killing you. I know this sounds harsh and it is.But Frankly, too many absentee siblings cause caregivers outragous guilt and  pain. most of it unnecessary if caregivers push back a litle. the sooner the better.</description>
      <author>Anonymous</author>
      <pubDate>Thu, 15 Oct 2009 14:20:10 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/parents-moving-in-with-you</guid>
      <link>http://www.caring.com/blogs/parents-moving-in-with-you/comments</link>
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      <title>Comment on Top 10 Breast Cancer Prevention Tips</title>
      <description>Two years ago the Canadian Cancer Society recommended that everyone take vitamin D3 to prevent cancer. The data on vitamin D preventing cancer is now as extensive as that on smoking causing cancer. Take a look at www.vitaminD3world.com for some good summaries of the data. How is it that folk still dont know about this and it gets no coverage</description>
      <author>tobylee02</author>
      <pubDate>Thu, 15 Oct 2009 02:26:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/preventing-breast-cancer</guid>
      <link>http://www.caring.com/blogs/preventing-breast-cancer/comments</link>
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      <title>Comment on Alzheimer's Phone Problems: Little Object, Big Headaches</title>
      <description>Thanks Kathy -- your lighter-side insights are one reason you've been in our Caring Currents blogroll for a long time now!</description>
      <author>Paula Spencer</author>
      <pubDate>Tue, 13 Oct 2009 22:23:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alzheimers-phone-problems</guid>
      <link>http://www.caring.com/blogs/alzheimers-phone-problems/comments</link>
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      <title>Comment on Senior Fraud Alert: Beware Financial Planners With Shady Credentials</title>
      <description>This was just one short post, and I plan to address more of these issues in future. I realize that some of these credentials, if added to the deep background of being a certified financial planner. However, my information, which was accurate, came from lawsuits filed around the country by people who have been defrauded by people with just the aforementioned credentials, so I believe this can stand as an important warning. The same goes with the insurance companies listed; yes they sell valuable policies and are represented by reliable agents. But they are also the companies turning up again and again around the country in class action lawsuits, and that's a red flag. Several of these lawsuits single out these companies for their pushy tactics in presenting products to seniors who may not need them or benefit from them. Again, I believe knowing this is useful to people as a warning to be cautious and investigate thoroughly before purchasing.</description>
      <author>Melanie Haiken</author>
      <pubDate>Tue, 13 Oct 2009 16:29:31 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/senior-fraud-alert</guid>
      <link>http://www.caring.com/blogs/senior-fraud-alert/comments</link>
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      <title>Comment on Alzheimer's Phone Problems: Little Object, Big Headaches</title>
      <description>My name is Kathy and I am the full time caregiver for my eighty one year-old Dad who has Alzheimer's and lives with me in North Carolina.

When my Mom died in 2004 and Dad moved in with me, I had no idea what to do.  But day by day, I found ways to cope, and even enjoy having my Dad with me.

So I started writing a blog at www.KnowItAlz.com, which shows the &quot;lighter&quot; side of caring for someone with dementia.

After a while, I added over 100 pages of helpful information and tips for caregivers.  We even have a Chat room so caregivers can communicate with each other from home.  Art and music are a very large part of my Dad's therapy.

Please pass this link along to anyone you feel would enjoy it.

Thanks!
Kathy Hatfield
</description>
      <author>kathyNC</author>
      <pubDate>Tue, 13 Oct 2009 15:43:44 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alzheimers-phone-problems</guid>
      <link>http://www.caring.com/blogs/alzheimers-phone-problems/comments</link>
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      <title>Comment on Alzheimer's Phone Problems: Little Object, Big Headaches</title>
      <description>My 83-year-old mother with dementia lives with me, and I have recently had to have directory assistance blocked on my phone (which unfortunately also required blocking the ability to make long distance calls).  My mother would call directory assistance over and over to get my work number, which is posted right by the phone.  Finally one month I received my phone bill and had over $30 of charges to directory assistance.  I hated to have to change my phone service, but just couldn't afford to take the chance that she would continue.</description>
      <author>annmartin</author>
      <pubDate>Tue, 13 Oct 2009 13:35:53 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alzheimers-phone-problems</guid>
      <link>http://www.caring.com/blogs/alzheimers-phone-problems/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>I am so grateful that Mom took the time to make decisions in advance, and took care of her advance directive, power of attorney, and all that.  What really annoys me is when the bank, insurance, government agencies etc that I have to deal with, all have different rules and procedures that make taking care of financial details more difficult.  Mom's bank won't accept the POA she did in advance; they want it on thier own form. She stopped being able to talk,walk, etc over 2 yrs ago, but I still can't close out her credit card account.  I walked into the local social security office, and with just my ID and say-so, they made me her rep-payee.  But I still can't get a copy of her original card - that she has to sign for herself. I can't switch her medicare advantage plan when we moved her to a new long-term care facility - but the rep at the facilty can do this, at my request, no questions asked. This part of caregiving really could be streamlined if all these agencies and businesses followed the same rules.</description>
      <author>Anonymous</author>
      <pubDate>Sun, 11 Oct 2009 01:42:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Flu Alert: 10 Warning Signs That It's Time to Call the Doctor</title>
      <description>This is so superficial!  Speak with MD offices and you get a total line of this...they have stock answers for everyone while having files available.  Your once over lightly here attests to a flippant attitude with nurses, care givers...and then MDs.  The medical system is in distress, and if confronted with the care &amp; concern put out like this article, it would be long time dead.</description>
      <author>calalillie</author>
      <pubDate>Sat, 10 Oct 2009 22:39:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/flu-alert</guid>
      <link>http://www.caring.com/blogs/flu-alert/comments</link>
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      <title>Comment on Senior Fraud Alert: Beware Financial Planners With Shady Credentials</title>
      <description>Great post,

I work on a blog that discusses senior aging in place ideas and in-home care. We are writing a series on scams that focus on the elderly. If you are reading this and want to learn more, check out that series at: http://www.rightathome.net/seniorhomecare/?p=297

Keep up the great posts,
Bill</description>
      <author>RightatHome</author>
      <pubDate>Fri, 09 Oct 2009 19:19:24 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/senior-fraud-alert</guid>
      <link>http://www.caring.com/blogs/senior-fraud-alert/comments</link>
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      <title>Comment on Heart Attack! Do You Know the Warning Signs?</title>
      <description>Great post. A very informative post detailing about all the consequences of heart attack. This is the most serious issue that can save lot of lives during the heart attack of cardiac arrest. In the cases of heart attack and cardiac arrest, or any other heart shocks, time sets to be the most crucial factor for the survival of the patient. Keith Churchwell has extraordinarily explained the pros and cons while handling patient suffering immediate heart attack or cardiac arrest in www.wellsphere.com/complementary-alternative-medicine-article/heart-attack-or-cardiac-arrest/610913. The response a person takes to treat a victim decides the probability of his/her survival. It&#8217;s been my personal experience fighting to survive against a heart attack. A quick recognization of your bodily responses may increase your chances of survival. Because of having many heart problems, I was enrolled in a concierge Healthcare program from elite health. I was attacked by a severe heart attack in a party, luckily surrounded by many people. Some of the sudden changes in my body was recognized by me and anticipated immediately. I got a very severe chest pain which was almost unbearable for more than a minute. I got the suspicion that I might be having heart attack, and immediately called my physician on the phone, and explained my condition and its severity. Because of the immediate guidance, I was directed immediately to have an aspirin which I used to carry with me as prescribed by my physician. It was quite a frightening experience for me to face such a heart attack, but somehow I managed to be calm until 911 arrived. I was immediately taken to the nearest hospital, where already my physician were present and have got everything setup according to my medical history. And it was in some matter of seconds that everything was in control. A doctor, who already have the complete knowledge of the medical history and fitness of the person, extra ordinarily ameliorate your recovery process. Hence such a concierge level program from Elite health, helped me a save my life, like many others. </description>
      <author>Brate Smith</author>
      <pubDate>Fri, 09 Oct 2009 11:41:34 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/heart-attack-do-you-know-the-warning-signs</guid>
      <link>http://www.caring.com/blogs/heart-attack-do-you-know-the-warning-signs/comments</link>
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      <title>Comment on Heart Health Alert: Higher Stroke Risk for Women With Atrial Fibrillation</title>
      <description>Although many people think of heart disease as a man's problem, women can and do get heart disease. I was in the same misconception regarding the heart disease, but was made aware by a medical checkup campaign.  In fact, heart disease is the number one killer of women in the United States. It is also a leading cause of disability among women.
The most common cause of heart disease is narrowing or blockage of the coronary arteries, the blood vessels that supply blood to the heart itself. This is called coronary artery disease and happens slowly over time. It's the major reason people have heart attacks. Prevention is important: two-thirds of women who have a heart attack fail to make a full recovery.

The older a woman gets, the more likely she is to get heart disease. But women of all ages should be concerned about heart disease. All women can take steps to prevent it by practicing healthy lifestyle habits.

Actually, right now I am suffering from a blockage in the coronary artery and was once blocked up to 85%. I got the stent implantation which is a mesh like spring which is used to broaden the artery and hence restoring back the blood flow. You can see further information regarding stent operation from www.heartsite.com/html/stent.html. I got to know everything regarding my stent operation from this site. I was really unaware of such a blockage. I sometimes feel dizzy, restless, lazy , but thought that to be something related to mental ability, and hence never worried about it. Once I got my basic medical checkup at Elite health medical office in Los Angeles. The ECG report went to be something suspicious. So, they advised me to have further advance diagnosis to determine and assure regarding the problem in the heart. After my MRI , CT scan and other such scans it came to me as a shock that I was facing a problem of blockage. It was quite surprising to me, and as I was not aware of anything regarding this, I was really frightened. The doctors explained me every information regarding my health and its treatment, and suggested me to have stent operation. That was some dreadful days of my life, which I faced only because I was careless about my health. It was my luck that I somehow went for a basic checkup at elite health, but every woman out there may not be so lucky.
</description>
      <author>Brate Smith</author>
      <pubDate>Fri, 09 Oct 2009 11:31:53 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/atrial-fibrillation-and-stroke-risk</guid>
      <link>http://www.caring.com/blogs/atrial-fibrillation-and-stroke-risk/comments</link>
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      <title>Comment on Caregiving Stress Buster: Your Top 10 Pet Peeves </title>
      <description>I smiled when I read these. I call my Mother (girlfriend) because when I call her Mother, she says I have no children. I used to mind but not any more. I think I have come a long way since the start of Mothers adventure. Some days still get to me though. She has mellowed the last few years as her dementia progresses. We are sharing, laughing, crying and all that comes with this stage.

Only thing that gets me now is lack of sleep!</description>
      <author>Anonymous</author>
      <pubDate>Thu, 08 Oct 2009 19:45:52 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/pet-peeves-about-eldercare</guid>
      <link>http://www.caring.com/blogs/pet-peeves-about-eldercare/comments</link>
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      <title>Comment on Flu Alert: 10 Warning Signs That It's Time to Call the Doctor</title>
      <description>Thanks for the post.  One thing I've not seen covered is how long is a person contagious to others ... prior to and also after symptoms?</description>
      <author>daccarte</author>
      <pubDate>Wed, 07 Oct 2009 19:47:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/flu-alert</guid>
      <link>http://www.caring.com/blogs/flu-alert/comments</link>
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      <title>Comment on Senior Fraud Alert: Beware Financial Planners With Shady Credentials</title>
      <description>Dear Ms. Haiken

Thank you for your recent article, Senior Fraud Alert.  We as an industry need to keep a constant vigil in this area.  However, your details were a bit off the mark in several important areas.

For example, the broad stroke with which you condemn six entire designations as &#8220;fraud&#8221; was just that, very broad and generalized.  I can only speak about the CRFA, Certified Retirement Financial Advisor, designation, but I can assure you that the curriculum involved in this program is of great value to senior clients across the country.  

I&#8217;ve been a CFP (Certified Financial Planner), a designation you apparently highly approve of, since 1991.  However, when I took the CRFA course it was quite a revelation.  The amount of overlap with the CFP material was perhaps 10%.  The time I spent in Dallas taking the classes, and studying the very thorough written materials that accompanied that training, was time very well spent.  I am confident that my clients have benefited greatly from its additional knowledge and insight.  

The specific areas that were not exactly accurate in your report include:

1. Many, if not most, CRFA candidates take the classes in person, not just via correspondence.  However, even those who choose to only receive the materials and self study still have to pass the same exam.  The exact same thing is true for CFP candidates.

2.  Yes, the exam is multiple choice, but so is the CFP exam.

3.  A simple exam?  Maybe not so much.  While not as comprehensive as the CFP exam it is in far greater detail and requires far greater expertise in the retirement planning area than the CFP.

And true enough, &#8220;if it sounds too good to be true&#8230;.&#8221; is a reasonable rule of thumb.  However, lambasting an entire sector of the financial service industry with such broad strokes, based upon what was obviously limited research, is hardly a rule of thumb our collective parents would have endorsed. 



P. Frederick deNapoli, CFP, CRFA
Peabody MA
</description>
      <author>P Frederick deNapoli</author>
      <pubDate>Tue, 06 Oct 2009 20:38:46 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/senior-fraud-alert</guid>
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      <title>Comment on Is It Okay to &quot;Spy&quot; on a Relative With Suspected Dementia?</title>
      <description>It has been our experience that often the elder loved one seems to rally in the presence of children.  (Like they are almost on good behavior, being careful not to slip up) This often makes the dementia hard to recognize. My father covered up Mom's dementia for years.  A trained Hospice nurse noticed and finally alerted me of Mom's condition.  My heart goes out to anyone having to cope with a parent lost to dementia; but recognizing the symptoms is the first step.  Caring.com has given me so many ideas and much needed support in dealing with my 82 year old mother.  Thank you.  </description>
      <author>Tootsie60</author>
      <pubDate>Tue, 06 Oct 2009 18:22:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/signs-of-dementia-are-showing</guid>
      <link>http://www.caring.com/blogs/signs-of-dementia-are-showing/comments</link>
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      <title>Comment on Is It Okay to &quot;Spy&quot; on a Relative With Suspected Dementia?</title>
      <description>Sadly this article hit home with our family. I am the &quot;terrible daughter in law&quot; because I tried to insist my mother in law be helped because of things I was told by her neighbors and friends. My husband agrees that something should be done for her best interests...but the siblings are all in denial of course. How DARE anyone say the word dementia?! Even though there are serious tell tale signs present, she is left alone to fend for herself. The family is in such conflict that my husband and I have not communicated with the siblings for over 2 and a half years. Since the one sibling is the durable power of attorney, we just bowed out gracefully, and we hope he will step in to do the right thing...so far, he has not. So sad to see that she was ruining herself financially, and is suffering so with paranoia, delusions, and olfactory hallucinations, but we have no control. I tried speaking to alzheimers assn, her doctor, the drivers license bureau (she still drives), all to no avail. I am waiting for the &quot;crisis&quot; to happen to jerk these guys out of their denial, but I hope it does not cause her or someone else harm or worse. Especially since she is diabetic, and has fallen on several occaisions.</description>
      <author>Jane F</author>
      <pubDate>Tue, 06 Oct 2009 14:33:36 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/signs-of-dementia-are-showing</guid>
      <link>http://www.caring.com/blogs/signs-of-dementia-are-showing/comments</link>
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      <title>Comment on Senior Fraud Alert: Beware Financial Planners With Shady Credentials</title>
      <description>I too am very concerned about frauduless representation among financial advisors, and as such have done my homework on the issue.  In doing so I recognized some errors in Miss Haiken's treatise.  First, the Certified Senior Advisor is a genuine certified credential, not a fraudulent one.  However, if this is the only professional or advanced credential utilized by a person dispensing financial advice,then I would go somewhere else.  The credential CSA can be earned by professions from many walks of life that work with seniors, such as medical counselors, spiritual counselors,attorneys,and financial specialists.  It's not a bad credential but it does not confer expertise in financial matters unique to seniors, and if a financial advisor has this credential in addition to other financial specialized training and credentials such as CFP, CLU, ChFC, etc., then it is a definate plus.  The same goes with the Certified Retirement Financial Advisor.  This organization is currently becoming certified by the same organization that certified CFP and CSA.  You can learn more about what these credentials mean and the advisors that obtain them can offer at their web sites; www.csa.com and www.crfa.com.  

Pertaining to the insurance companies listed, Miss Haiken suggested that they endorse fraudulent credentials and by association support financial advisors holding fraudulent credentials and are involved in scams.  She is way off base on this.  All insurance companies have lists of approved credentials that their agents or financial advisors can use when representing their products to the public, or when holding public forums.  The companies specifically say that advisors cannot use any credentials not on the approved list.  Most companies have their approved lists on their web sites.

I have found that the best financial advisors are those who are independent and not affiliated with or paid by a financial investment, insurance, or brokerage companies, that have been in business for at least 15 -20 years, and that have an understanding of the differences in the unique financial requirements and outlooks of senior versus folks who are still working.  A good advisor will not only know about sensible investments, but also about taxes and estate matters, and be willing to conduct meetings that include the seniors children present.</description>
      <author>pwood</author>
      <pubDate>Mon, 05 Oct 2009 19:48:33 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/senior-fraud-alert</guid>
      <link>http://www.caring.com/blogs/senior-fraud-alert/comments</link>
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      <title>Comment on Baby Love: Therapy for Alzheimer's Sufferers </title>
      <description>It's wonderful that it is ackinowledged dolls help women but since I care for my spouse, what is recommended or works for men for the same purposes? Will appreciate any ideas or known things that have worked for the men. Thanks</description>
      <author>stress</author>
      <pubDate>Sat, 03 Oct 2009 15:10:11 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/therapies-for-alzheimers-sufferers</guid>
      <link>http://www.caring.com/blogs/therapies-for-alzheimers-sufferers/comments</link>
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      <title>Comment on Sex and Alzheimer's: Love Stories, Sad Stories, and Lots of Questions </title>
      <description>WellSpouse thanks for adding your perspective -- coincidentally I just mentioned your organization in a newer post about why spousal caregivers often miss out on resources for help. </description>
      <author>Paula Spencer</author>
      <pubDate>Fri, 02 Oct 2009 18:36:21 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sex-and-alzheimers</guid>
      <link>http://www.caring.com/blogs/sex-and-alzheimers/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>There are seven of us --- our Mom has dementia and is getting really bad.  Our Dad died almost two years ago.  Things have gotten really ugly and we're all trying to stay away from each other.   I have Power of Attorney as far as Mom is concerned.  We sent it up years ago ---- when she couldn't remember the woman our Dad left her for!  Never thought I'd see that day!  I've had siblings tell me that Power Of Attorney Sucks!  They don't think its right or fair.  Having that responsiblity isn't all that fun --- but I can see the need for it.  There is rarely one of us that agree on anything pertaining to our Mom's care.  I try to be fair --- discussing most everything with all of them.  There has never been a time that all seven of us have agreed on one thing!  There have been times I think Mom should be on some kind of anti-depressant or anti-psychotic meds --- half go along with that and the other half just have a fit!  I've always tried to include them in deciding where our Mom should live.  Two -- who work full time,  wanted to take her home with them.  I'd had her home with me several times,  and I felt she wasn't safe with any of us after a while.   So we had to put her in a rest home (Medicaid Rules) for 3  months  to begin with.   She was able to go to a Level One Assisted Living but not for long.  She's been in a Level Two now for a good 10 months -- but things are not looking all that great there.  She may have to move to a lock-down Alzheimer's Unit here soon.  She's fallen several times in just the last month and something has changed in her brain.  She's lucky she has never broken any bones when she's fallen.  But --- I guess what I really need to get out is that no matter what I do or what I decide,  I'm the bad person.  My Mom gave me the Power and I feel she expects me to do the best I can with it ---which would include her saftey and care.  At some point,  no matter what any of the others think --- I have to make what I think is the best decision for our Mom.  It makes some furious --- and I've been called alot of things because of it.  But --- in the end --- after what happened with our Dad --- and now all this thats going on with our Mom --- I doubt there will be many who will ever speak to the others again.  I'm not so sure thats a bad thing.  </description>
      <author>Anonymous</author>
      <pubDate>Fri, 02 Oct 2009 04:30:22 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on Sex and Alzheimer's: Love Stories, Sad Stories, and Lots of Questions </title>
      <description>A very perceptive entry. I am the President of the Well Spouse Association, http://wellspouse.org, a non-profit group offering peer support to husbands, wives or partners of persons with chronic illness and/or disability. We have members whose spouses have Alzheimer's or other illnesses involving dementia. That apart, very often in the case of any chronic illness/disability, intimacy gets disrupted, due to fatigue and other symptoms that make it less interesting or possible for the ill spouse, and less appealing or attractive for the well spouse.

The situation described by pollytnjc certainly can  occur. Usually it's the family who takes exception to the &quot;abuse&quot; of a new spouse/caregiver.  

The WSA concentrates on helping the well spouse regain balance in his/her life in order to help them look after their ill spouse. This principle applies no matter what the situation. So in the case of dementia and Alzheimer's, I would say we would encourage the well spouse so that the emotional well-being of both partners is paramount. </description>
      <author>Wellspouse</author>
      <pubDate>Fri, 02 Oct 2009 01:43:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sex-and-alzheimers</guid>
      <link>http://www.caring.com/blogs/sex-and-alzheimers/comments</link>
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      <title>Comment on Baby Love: Therapy for Alzheimer's Sufferers </title>
      <description>Thanks Paula for your comment.  I will plan to get my mother a baby doll for christmas this yr.  As you said, now she will love it as a cute gift, later this gift may comfort her.  </description>
      <author>dancingbird</author>
      <pubDate>Thu, 01 Oct 2009 22:15:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/therapies-for-alzheimers-sufferers</guid>
      <link>http://www.caring.com/blogs/therapies-for-alzheimers-sufferers/comments</link>
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      <title>Comment on Baby Love: Therapy for Alzheimer's Sufferers </title>
      <description>My grandmother passed away at 101 years of age and in her final year she was given a life size doll which she absolutely loved.  This is such a comfort.  Any suggestions for me?</description>
      <author>LeslieAB1</author>
      <pubDate>Thu, 01 Oct 2009 17:08:20 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/therapies-for-alzheimers-sufferers</guid>
      <link>http://www.caring.com/blogs/therapies-for-alzheimers-sufferers/comments</link>
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      <title>Comment on Caring for a Spouse? 5 Reasons Stressed Spousal Caregivers Miss Out on Help</title>
      <description>Great Article Paula,

That was very insightful, I especially liked the part about how spouses might not even think that what they are doing is caregiving. They might not see the role that way. We all know that caregivers need time apart from the care recipient. I would add the the resources that you listed, at least one nation-wide, trusted caregiving organization. Maybe one like Right at Home. Check out our blog for more info on caregivers at http://www.rightathome.net/seniorhomecare.

Keep up the great articles Paula,
Bill</description>
      <author>RightatHome</author>
      <pubDate>Thu, 01 Oct 2009 15:34:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caring-for-a-spouse-and-missing-out</guid>
      <link>http://www.caring.com/blogs/caring-for-a-spouse-and-missing-out/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>My husband has no contact with any of his 3 brothers, and has not for almost 3 years now. It stems from disagreements regarding the care of their mother who was diagnosed with dementia about 5 years ago. The brother that has the durable power of atty for everything thinks she is &quot;just fine&quot;, so she has been left to her own devices all these years. She is 83, has fallen, which required a surgery to repair injuries, had a quad by pass 3 yrs ago, 2 knee replacements, and is a diabetic. She also is &quot;scammed&quot; frequently by &quot;doctors&quot; in magazines that sell her cancer cures, and every herb possible, which is not supposed to be mixed with high blood pressure meds. She has gotten so far into debt from home shopping and credit cards that her paid off house has been refinanced about 3 times. The last I knew her debt was up to $20,000. She is on fixed income of course, lives alone. She has hit a parked car in a lot, ripped off part of it, dragged it behind her...but was not even aware until police were waiting outside the store for her! She also has forgotten to pay bills, and now does not have the ability to write check numbers in her bank book, let alone balance it. She calls the police, or writes them letter because she has delusions about homeless people sleeping in her car. She is still driving even though my husband thinks she should be made to go take a test at the DMV for safety reasons...the dpoa refuses to address it. Guess he will wait until she hurts or kills herself or someone else before he takes the keys away. She has no caregiver at all, and this sibling is well over an hour away. The others live over 400 miles away, and one clear on the West coast (we are midwest). We feel there should be a discussion and steps should be taken to get her help to come in the home part time, her finances need to be taken over by the dpoa, and definitely the car keys taken is my guess. So, the siblings are mad because they just want her left alone, and we do not agree. They think we just want her tossed right into a nursing home, and that is not true. Eventually that may be the step, but not yet. It is a real shame that the family is split because a few want to stick their head in the sand and ignore the problems she is having. It is really not in her best interest, which is the most important issue isn't it? It is about HER.</description>
      <author>Jane F</author>
      <pubDate>Thu, 01 Oct 2009 15:23:11 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on Heart Health Alert: Higher Stroke Risk for Women With Atrial Fibrillation</title>
      <description>I have had atrial fib for approx 10 years - In June 2008, I had a small blood clot in my brain, thank God my husband was home and got me to the hospital quickly and I got the tpa drug, which worked, and I am so lucky to not have any side effects.  I am on blood thinners now.  I have been on atenolol and rythmol for several years and it still did not totally control my atrial fib.  After I had the stroke, I requested a sleep study and was diagnosed with severe obstructive sleep apnea.  Since April (5 months ago), I have been sleeping with a CPAP machine and I have not had one atrial fib since I've been using the CPAP.  I went on the internet and looked up Atrial Fib &amp; Sleep Apnea and was surprised to see how these two things can go together.  When I told my heart doctor, all he said was that yes, sometimes AF is caused by sleep apnea.   I asked, why didn't he tell me that instead of pushing meds and ablation.  I just wanted all of those 22 million people who have AF to know about this and to get a sleep study to see if they have apnea and need a CPAP machine. Amazing what the drs. don't tell you!
It took me about 3 weeks to get used to the CPAP machine, but now I sleep better and feel better and would not be without it.  </description>
      <author>Rita.Rupert</author>
      <pubDate>Thu, 01 Oct 2009 14:34:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/atrial-fibrillation-and-stroke-risk</guid>
      <link>http://www.caring.com/blogs/atrial-fibrillation-and-stroke-risk/comments</link>
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      <title>Comment on Baby Love: Therapy for Alzheimer's Sufferers </title>
      <description>my mother just pasted away a few months ago from 8yrs of dementia. her last 4 yrs was in a nursing home. shortly after she was there, i bought her a cute bunny with floppy ears it was the size of a small baby. that was the best present i ever bought her. she loved and cared and talked to that bunny like it was her baby. i believe thats what kept her company and kept her going for 4 more yrs. when she died i wanted the bunny to go with her but i changed my mind at the last minute and decided to keep her with me for my memories.</description>
      <author>serioussue</author>
      <pubDate>Wed, 30 Sep 2009 19:03:40 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/therapies-for-alzheimers-sufferers</guid>
      <link>http://www.caring.com/blogs/therapies-for-alzheimers-sufferers/comments</link>
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      <title>Comment on Baby Love: Therapy for Alzheimer's Sufferers </title>
      <description>dancingbird, I think that when and how people respond to doll therapy varies by individual. She might enjoy it at first just as a sweet gift, as many women collect dolls, and then may or may not take greater comfort in it as time goes by. </description>
      <author>Paula Spencer</author>
      <pubDate>Tue, 29 Sep 2009 21:43:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/therapies-for-alzheimers-sufferers</guid>
      <link>http://www.caring.com/blogs/therapies-for-alzheimers-sufferers/comments</link>
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      <title>Comment on Baby Love: Therapy for Alzheimer's Sufferers </title>
      <description>My mother is not &quot;there&quot; yet, but I recall how a babydoll really helped my grandmother years ago.  She loved that babydoll, and altho she didn't carry it around, she enjoyed having it in her room, and she would laugh about it like she was &quot;in&quot; on some joke, but it always made her smile.  I'm all for what works!  Course, with me, its probably going to have to be Johnny Depp or Paul McCartney doll.....</description>
      <author>pollytnjc</author>
      <pubDate>Tue, 29 Sep 2009 18:05:40 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/therapies-for-alzheimers-sufferers</guid>
      <link>http://www.caring.com/blogs/therapies-for-alzheimers-sufferers/comments</link>
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      <title>Comment on Baby Love: Therapy for Alzheimer's Sufferers </title>
      <description>My mom is in the later moderate stage of Alzheimers, would a baby doll soothe her now?  Or is the doll therapy best received and helpful when in the late stage?

Thanks! </description>
      <author>dancingbird</author>
      <pubDate>Tue, 29 Sep 2009 15:41:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/therapies-for-alzheimers-sufferers</guid>
      <link>http://www.caring.com/blogs/therapies-for-alzheimers-sufferers/comments</link>
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      <title>Comment on Baby Love: Therapy for Alzheimer's Sufferers </title>
      <description>My agency provides care for an elderly woman in the later stages of Alzheimer's, and she loves her baby doll.  I'm glad to see that this is recognized as a good therapy for her.  We also use Baby Einstein DVDs to entertain her and play with paper dolls with her.  She also responds well to very simple puzzles.</description>
      <author>LKN Caregiver</author>
      <pubDate>Tue, 29 Sep 2009 13:19:08 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/therapies-for-alzheimers-sufferers</guid>
      <link>http://www.caring.com/blogs/therapies-for-alzheimers-sufferers/comments</link>
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      <title>Comment on Why You Should Worry When Your Parents Mention the Word Annuity</title>
      <description>Saying that Annuities are in all cases bad for seniors is absolutely wrong.  the above article, pitching class action attorneys at the end, sounds highly suspect to me. We all know that someone nets about $6 from any class action case! The big winners are the attorneys! Back to the annuities -- if you thing that 3-8% is a HUGE commission, you know little about the insurance field.  there are other products, such as wrap accounts that pay upwards of 18% for the first year and additional commissions thereafter! Are annuities right for someone with lower incomes, probably not. But to classify that they are wrong for ALL seniors fails to consider their individual position and goals.  And while they do, often, carry a guaranteed death benefit, they are NOT the same as life insurance.  
Absolutely, take your time, and know the product you buy, that is the buyers responsibility, after all you are signing a contract.  KNOW what you are signing, but for heavens sake, don't lump all seniors' and their needs into one category. </description>
      <author>Anonymous</author>
      <pubDate>Tue, 29 Sep 2009 05:41:52 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/annuity-fraud</guid>
      <link>http://www.caring.com/blogs/annuity-fraud/comments</link>
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      <title>Comment on Why You Should Worry When Your Parents Mention the Word Annuity</title>
      <description>I unfortunately helped my parents sign up for a fixed annuity when we went in to buy some CDs at our local bank. I didn't understand what we were buying and couldn't reach my brother, who might have known more. I STILL feel guilty about it.

I will NEVER forgive the bank for talking us into that. We were able to get our money out after six years, but the trust I had with the bank is gone forever. Annuities are INSURANCE policies, and pay a BIG commission to the salesperson. SHAME on the sellers for taking advantage of seniors. 

My big lesson is TAKE YOUR TIME to research something if you don't understand it. Don't give in to high pressure sales. </description>
      <author>HandiAnn</author>
      <pubDate>Mon, 28 Sep 2009 13:06:11 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/annuity-fraud</guid>
      <link>http://www.caring.com/blogs/annuity-fraud/comments</link>
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      <title>Comment on What Is Hospice? And Why Hospice Needs a PR Campaign</title>
      <description>My husband has been in hospice for palative care for about 4 months now.  I cannot tell you what a terrific help they have been.  He has equipment he needs, his meds are monitored, I can talk to a case manager and a social worker, and he has a regular shower nurse who specializes in body checks for sores and bruising.  I could not manage at this point even though he is in a memory support unit without their help.  They help me a great deal in communicating to the facility what is needed and following through.  God bless them.  My recommendation, enter as soon as your doctor feels that you qualify.  You can also leave hospice and come back if necessary.</description>
      <author>Joy Golliver</author>
      <pubDate>Sun, 27 Sep 2009 23:21:05 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-is-hospice</guid>
      <link>http://www.caring.com/blogs/what-is-hospice/comments</link>
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      <title>Comment on Compassion Fatigue: To Stop Caregiving Stress, Stop Caregiving</title>
      <description>It is very important for me (and others) to remember that we all have limits and boundaries and that honoring them is very important. This is a major part of my life and I appreciate your advice. 

Courtney_182 www.shiftshappen-site.com</description>
      <author>Courtney_182</author>
      <pubDate>Sun, 27 Sep 2009 23:20:25 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/compassion-fatigue</guid>
      <link>http://www.caring.com/blogs/compassion-fatigue/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>I found it interesting to read the other comments.  I have been extremely down lately and sometimes you wonder if anyone understands. My mom has dementia and two years ago is when it just seems like everything 'hit the fan'.  My mom lived alone and fell, had to there started to be other signs that 'things were just not right'.  Along with the fall that got the ball rolling, she was not taking her medication as prescribed, not eating meals like she should.  I live 20 miles away, organized &quot;Meals on Wheels&quot; to come by so she would get a good dinner and went over about every day - or every other is my sibling could stop by in between.  My sibling and I always got along, although we are very different from each other.  The day my mom fell was like the bottom fell out of my world.  My brother is very nice when he wants something, the minute he gets what he wants - he's back to non-contact.  We moved my mom two miles from him and his family and she is now 40 from my husband and I.  I didn't feel it accomplished anything to have my mom in middle - what if she needed us right away?  She is in assisted living.  My sibling does see her every day after work for an hour or two, my adult nieces that live near her NEVER stop by to see her or both to call.  Everything she had that couldn't go to her new place, my sibling decided it was to become property of my nieces.  All her bills, mail go to her house - even though he's two miles away.  He has Power of Attorney that was set up a long time ago.  I see my mom once or twice a week and drive the 80 miles round trip, not to mention when I take her out while I'm there.  And he STILL has the nerve to not keep me posted as to what is going on with my mom.  I call her every single day.  She mom's dementia is not so bad that she doesn't know me - she always says how she loves when I visit - she, unfortunately, can't remember any event after it happens.  She could never remember if they went to the bank, what they did while there, anything.  Then if you try to talk to him reasonably, he gets mad - in hopes, I'm sure, that you won't want to approach him.  Does anyone have any suggestions?  I am hurt to think after all these years that our relationship would come to this.  He is always so quick to 'get even' with someone.  I have a feeling that he has been mad ever since my mom went into assisted living because he's always so concerned that her money 'take care of her the rest of her life' - yet, she has a LOT!  Why would she not use it to go into assisted living?  I think he feels that since I don't work and my husband and I don't have kids, we should have taken my mom in - yet, he would never let me handle anything - it would strictly be to keep his inheritance going.  I am just perplexed most of the time to think that I have no other family and they really don't even care.  Not to mention how hard it is to see your own mother go through this disease and have to be so dependent on others - that would not have been her choice.  I love her dearly.</description>
      <author>kittymom</author>
      <pubDate>Sun, 27 Sep 2009 20:59:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on Compassion Fatigue: To Stop Caregiving Stress, Stop Caregiving</title>
      <description>Just to let you know....I went on vacation for 4 days.  It was wonderful.  I needed it immensely but when I got back, I got another &quot;bomb&quot; dropped on me..my unwed daughter who is 27 is pregnant...(what doesn't kill us makes us stronger right?).  She is also working as a waitress and the boyfriend of one month says he will help (we can only hope) but now I can add the possibility of babysitting my new grandchild to my list of responsibilities (I don't need any more responsibilities) but I already told mom that this may change some things and I know that I will want to be there for my new grandbaby and my daughter.  And she is an adult ....know of any really good sleep aids cause I'm tired of not sleeping!!!! And it's not getting better!!!  But after my rest, I really do feel better able to cope...(when can I plan my next vacation)  And I will really try to keep my sense of humor and as my mom says...try to think of that little bundle of joy coming into our lives...My mom is such a mom...Her response was that my daughter will probably make a real good mother.  Keep sedative suggestions coming..ok???</description>
      <author>PT Cruzr</author>
      <pubDate>Sun, 27 Sep 2009 12:02:52 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/compassion-fatigue</guid>
      <link>http://www.caring.com/blogs/compassion-fatigue/comments</link>
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      <title>Comment on Compassion Fatigue: To Stop Caregiving Stress, Stop Caregiving</title>
      <description></description>
      <author>PT Cruzr</author>
      <pubDate>Sun, 27 Sep 2009 11:53:47 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/compassion-fatigue</guid>
      <link>http://www.caring.com/blogs/compassion-fatigue/comments</link>
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      <title>Comment on What Is Hospice? And Why Hospice Needs a PR Campaign</title>
      <description>We just put my sister on Hospice this week. The nurse came to visit on tuesday and my sisters bloodpressure was 70/40. Immediately she was admitted to the Hospice center and her pain was managed,she was given a steroid to help with inflamation and now she is able to eat. she is so much happier and plans to be discharged from the hospice center and continue care at home till she needs to go back to the center for final stages of life. the ride to the center and back was picked up by medicare, the vns is also paid. its nice to know someone is helping to look after her when family cannot be close by</description>
      <author>Pattycakes</author>
      <pubDate>Sat, 26 Sep 2009 20:08:57 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-is-hospice</guid>
      <link>http://www.caring.com/blogs/what-is-hospice/comments</link>
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      <title>Comment on What To Do When a Family Disagreement Makes Caregiving Way Harder Than It Needs To Be</title>
      <description>I am learning that in our family dynamic, it is almost better to say less than more. We have the same issues -- daughters do most of the work, but the sons do most of the criticizing (&quot;you know what mom needs is....&quot;), even though the sons may not have had any contact (phone or in person) for weeks.   
  I used to spend a lot of energy (phone calls, emails, etc) trying to get my siblings involved.  I would say things like &quot;you haven't been here for six weeks&quot; or &quot;I check their caller ID and you never call&quot;.  I used to send out really lengthy emails with details about doctor visits, meds, etc.  All totally a waste of time -- they either never read it or else would criticize it.  
  So my new strategy is to act stupid and ask for suggestions. &quot;The doctor thinks maybe mom's irritation is due to depression.  Do you think that could be right?&quot;  &quot;Mom has trouble getting up the stairs to go to bed at night - what do you think we should do?&quot;.  
  What I am finding is that the siblings seem to be more involved.  They call her up to see if she sounds depressed.   They help her up the stairs to see if she really has trouble.  They are still full of &quot;you should do this or that&quot; comments, but I am sensing a more cohesive family unit trying to pull together for the sake of what is best for mom, rather than the brother/sister rivalry.  
  I'm also trying the positive reinforcement plan as well, with lots of &quot;mom told me how great it was to see you over the weekend&quot; comments.  
  There's a book called &quot;The Dance of Anger&quot; by Harriet Lehrer that basically says arguments will have the same script.  If one person changes, then the 'dance' changes, which can thereby change the outcome.  
   best of luck -- we are all feeling our way along.. 

</description>
      <author>Nitwit</author>
      <pubDate>Fri, 25 Sep 2009 18:10:04 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be</guid>
      <link>http://www.caring.com/blogs/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be/comments</link>
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      <title>Comment on What To Do When a Family Disagreement Makes Caregiving Way Harder Than It Needs To Be</title>
      <description></description>
      <author>Anonymous</author>
      <pubDate>Fri, 25 Sep 2009 18:01:19 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be</guid>
      <link>http://www.caring.com/blogs/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be/comments</link>
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      <title>Comment on Coenzyme Q10 Supplement Shows Promise In Preventing or Halting Parkinson's</title>
      <description>My father is 71 yrs old and was diagnosed with Parkinsons a year ago. I try to get information ont he dieases and try to keep him imformed</description>
      <author>arizonababydoll2</author>
      <pubDate>Fri, 25 Sep 2009 17:15:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/coenzyme-q10-supplement</guid>
      <link>http://www.caring.com/blogs/coenzyme-q10-supplement/comments</link>
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      <title>Comment on Coenzyme Q10 Supplement Shows Promise In Preventing or Halting Parkinson's</title>
      <description></description>
      <author>arizonababydoll2</author>
      <pubDate>Fri, 25 Sep 2009 17:13:46 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/coenzyme-q10-supplement</guid>
      <link>http://www.caring.com/blogs/coenzyme-q10-supplement/comments</link>
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      <title>Comment on Compassion Fatigue: To Stop Caregiving Stress, Stop Caregiving</title>
      <description>This is a helpful article, but please remember that not all family caregivers are children caring for parents, some of us are spouses caring for our husband or wife.</description>
      <author>pamsc</author>
      <pubDate>Fri, 25 Sep 2009 14:06:24 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/compassion-fatigue</guid>
      <link>http://www.caring.com/blogs/compassion-fatigue/comments</link>
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      <title>Comment on Compassion Fatigue: To Stop Caregiving Stress, Stop Caregiving</title>
      <description>Ohhhh how i relate to this. My 96 year old mom still lives at home with 24 hour care on rotating shifts (medicaid). I am the only child living nearby. Even with her 24 hr. care, the stress on me, the &quot;worry time&quot;, the errand running, shopping, dr. appts with her, plus working full time (in a job that is also in jeopardy) are finally taking their toll on me after 10 years (when my dad only died 2 years ago). Suddenly, this past August, I got a terrible cough, followed by a kidney stone, followed by some sort of stomach virus and exaccerbated reflux symptoms. I was a mess physically and mentally. Now I was also worried about my own health,not only my mom's. I am certain all of these ailments are stress related. One by one they are being followed up and taken care of, but the stress continues. I can sympathize with everyone here. The guilt, the stress: it's universal....it's not Jewish, it's not Italian, etc...it just IS. We must find coping skills and a support system to carry us through. This too shall pass.</description>
      <author>Anonymous</author>
      <pubDate>Fri, 25 Sep 2009 13:31:26 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/compassion-fatigue</guid>
      <link>http://www.caring.com/blogs/compassion-fatigue/comments</link>
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      <title>Comment on Are There Early Symptoms of Pancreatic Cancer? Yes!</title>
      <description>This article was so informative for me.  To my surprise, I do have a couple of these symtoms and I am going to see to it that my doctor have me tested for this type of cancer.  Thank you!</description>
      <author>dkp2654</author>
      <pubDate>Thu, 24 Sep 2009 11:23:27 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/early-symptoms-of-pancreatic-cancer</guid>
      <link>http://www.caring.com/blogs/early-symptoms-of-pancreatic-cancer/comments</link>
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      <title>Comment on What To Do When a Family Disagreement Makes Caregiving Way Harder Than It Needs To Be</title>
      <description>Our family conflict was so bad that we have not had contact with my husbands brothers for over 2 and a half years. The son that is durable power of attorney has his head stuck in the sand about their 83 year old moms health issues. My husband and I live 20 minutes from her, the dpoa lives over an hour away, the others are 3000 miles away and 500 miles away. I was doing a lot of the caring for my mother in law until she decided I was &quot;stealing&quot; all her stuff, like lotion, Bible bookmark, and most recently (even though I have not spoken to her or been to her house in over 2 yrs, her eye exercise video!. My husband and I wanted to have her checked out by a neurologist because she does have a diagnosis over 4 years old of dementia, but they are all in denial about that. She began several years ago with smelling things in her house, then other houses, then the car. It got so bad she was calling the gas company constantly and 911. Even after a new furnace and 3 chimney liners in as many months, she was not satisfied, so she went most of the winter with the heat off. She has hit a car in a parking lot, ripped a part of it off and was dragging it behind her car, but was totally unaware...until police were waiting for her when she came out of the store. This was 4 or 5 years ago. She has hit the fence separating her yard from a neighbors, and I know this because her driveway is by the fence, the neighbors have no drive way, they park on the street. She writes letter to police chief claiming there are homeless people sleeping in her car, she puts spike nails sharp side up around her fence perimeter, which the city made her remove. She was sure there were people stealing her tomatoes! She falls frequently, and has had surgery on an arm from the fall. She also had quad bypass surgery 3 years ago, is diabetic (but claims that is a lie, the doctor is in a cospiracy), so she eats whatever she wants and does not control blood sugars. She also has high blood pressure and is on meds for that, but she insists on buying scam &quot;herbs&quot; and cancer cures from phony &quot;doctors&quot; that send her magazines to order from. She orders stuff, then calls the credit card company saying it is identity theft because she does not remember doing it! She lines up soap bottles in her basement and takes lids off, and then accusing my husband of breaking in and doing it. But my husbands brothers say there is nothing wrong with her! She lives alone, still drives, and has control of her finances even though she has had to refinance her house 3 times for credit card debt to Home Shopping and &quot;herbs&quot; etc. We cannot resolve this family conflict because the brothers refuse to acknowledge that she needs to be checked by DMV to see if she should be driving, and she definitely needs a neurologist and gerontologist to look her over really good. They all refuse. They have made me feel like I am crazy or something for thinking there could be anything wrong with their mom, even though she calls and accuses me of stealing from her, and even reports me to the police for it! Advice????</description>
      <author>Jane F</author>
      <pubDate>Thu, 24 Sep 2009 08:02:01 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be</guid>
      <link>http://www.caring.com/blogs/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be/comments</link>
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      <title>Comment on Are There Early Symptoms of Pancreatic Cancer? Yes!</title>
      <description>My husband died of pancreatic cancer at the age of 58. Some of the symptoms that were mention, my husband had, at stage 4.  He did not have early symptoms.  He had gone to the doctor in November of 05, they found the tumor on the head of pancreas in December. He was given a year and a half, he died a year and a half later. He did not have early symptoms.</description>
      <author>one flower</author>
      <pubDate>Wed, 23 Sep 2009 09:45:31 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/early-symptoms-of-pancreatic-cancer</guid>
      <link>http://www.caring.com/blogs/early-symptoms-of-pancreatic-cancer/comments</link>
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      <title>Comment on Sex and Alzheimer's: Love Stories, Sad Stories, and Lots of Questions </title>
      <description>My father's sexual needs grew so much that he wanted sex all the time. My mom as his care giver gave in for a long time but after he proceeded to the next stages and became very aggressive he had to be moved to an Alzheimer's Facility. It was not condusive to sex and privacy so the sexual activity stopped. My father, of course didn't understand so he would become angry and accuse my mother of having a boyfriend. It became very ugly at times. We didn't want to put my mother in danger and we didn't know how to handle the whole situation. What do you do when the Alzheimer's &quot;victim&quot; is so angry and aggressive? Unfortunatly we lost my dad in 2008, but maybe someone else could benefit from some insight. </description>
      <author>lmartin</author>
      <pubDate>Tue, 22 Sep 2009 13:59:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sex-and-alzheimers</guid>
      <link>http://www.caring.com/blogs/sex-and-alzheimers/comments</link>
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      <title>Comment on Sex and Alzheimer's: Love Stories, Sad Stories, and Lots of Questions </title>
      <description>No, but I have seen love affairs start up in assisted living homes between residents married to others, very sexual conversations by a man to visitors and staff alike, and strong sexual approaches to caregivers, causing them to quit.  These are probably more prevelant.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 22 Sep 2009 13:54:20 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sex-and-alzheimers</guid>
      <link>http://www.caring.com/blogs/sex-and-alzheimers/comments</link>
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      <title>Comment on Sex and Alzheimer's: Love Stories, Sad Stories, and Lots of Questions </title>
      <description>Further, what about a situation where a person with sexual desires and slight dementia is perceived to have a good deal of money, and a caretaker is able to use sexual favors to gain control of this person's resources?  Has anyone had experience within their family situations where a caregiver has abused their position like this?  Or similar situation where an elderly person has been manipulated this way?  </description>
      <author>pollytnjc</author>
      <pubDate>Tue, 22 Sep 2009 13:35:03 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sex-and-alzheimers</guid>
      <link>http://www.caring.com/blogs/sex-and-alzheimers/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>My prayers to his family.  My husband was 56 when he was told he had pancreatic cancer.  He passed away after 18 months of the disease.  This is a terrible cancer, I wish that a cure will be found soon. </description>
      <author>one flower</author>
      <pubDate>Sun, 20 Sep 2009 18:45:23 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>As on who was married to someone who lost a father to lung cancer at 36, I can identify with the loss that those who question God at moments such as this in taking a life so young really in comparison as he was.  And by the way smoking was not what his family members blamed for the death, although he was a smoker - but five other members of his immediate family also died of cancer in one form or another, and many very young so genetics too played a part.

I just hope they can find the gene eventually and maybe that will lead to the cures, rather than always blaming either lifestyle, or the luck of the draw.  Because if it is genetic, than that luck and gene just might be changed.</description>
      <author>betsy ross</author>
      <pubDate>Sat, 19 Sep 2009 08:15:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Financial Crises for Caregivers: The Time vs. Money Dilemma</title>
      <description>Well if this was a perfect world than maybe we as caregiver would have help with taking care of your love ones but it is not.  I am the oldest of six and I have been caring for my dad for almost seven years.  Not even a vacation.  You can not make grown people do anything so I have told myself it i what it is and i take care of my dad because I am all he has.</description>
      <author>msann13</author>
      <pubDate>Sat, 19 Sep 2009 08:14:18 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/financial-crises-for-caregivers-the-time-vs-money-dilemma</guid>
      <link>http://www.caring.com/blogs/financial-crises-for-caregivers-the-time-vs-money-dilemma/comments</link>
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      <title>Comment on How Caregiving Can Help You Live Longer</title>
      <description>How nice for people caring for a spouse or partner.  However, I suspect the opposite may hold true for those of us in the Sandwich Generation caring for parents.  Any studies on that?</description>
      <author>GALOWA</author>
      <pubDate>Sat, 19 Sep 2009 05:06:26 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-caregiving-can-help-you-live-longer</guid>
      <link>http://www.caring.com/blogs/how-caregiving-can-help-you-live-longer/comments</link>
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      <title>Comment on Middle-Age, um, Moment</title>
      <description>If, in fact, you are correct, THANK GOD... !</description>
      <author>GALOWA</author>
      <pubDate>Sat, 19 Sep 2009 04:50:02 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/middle-age-moment</guid>
      <link>http://www.caring.com/blogs/middle-age-moment/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>First my deepest sympathys go to  his family and friends..I would like to say that he was a very kind man from what i seen and to have someone pass on after making so many people happy is a shame. Some times i ask God why all the good ones have to be taken..such as my dad..He may have battled cancer and lost but he will forever remain in our hearts and minds..God Bless Him and his family and may the lord give you all strength to keep going.</description>
      <author>countrygirl94_lookin</author>
      <pubDate>Sat, 19 Sep 2009 03:00:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>Patrick's valor against this dreaded disease was strong and as vibrant an steadfast as the marvelous artistry as a dancer. He'll be missed, though never forgotten.</description>
      <author>Heathergrey</author>
      <pubDate>Sat, 19 Sep 2009 01:05:44 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>BEYOND, THE USUAL ACCODALES FOR PATRICK, I BRIEFLY READ HIS BATTLE ALSO WITH THE ONLY TOO PRESENT TERM OF ALCOHOL ABUSE WHICH IS NOT A CONDENMATION  BUT AN UNDERSTANDING OF LIFE'S PRESSURES, AS AN ACTIVE MEMBER OF ALCOHOLICS ANONYMOUS, I SALUTE PATRICK AND SOBERLY PLAYED &quot;GHOST&quot; TWO NIGHTS AGO&quot; AS A TRIBUTE TO A TREMENDOUS HUMAN BEING BEYOND THE USUAL GALLERY OF SELFISH AND UNSTABLE ACTORS/ACTRESSES OF THIS PERIOD ,MARIO</description>
      <author>JOHN PAYNE</author>
      <pubDate>Sat, 19 Sep 2009 00:58:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>My thought and prayers go out to Lisa and her family. I can't believe the most wonderful people have to leave this world before what seems to be way before their time. I personally know exactly what it's like, as this same loss has happened to our daughter and me. Stay close to those you are most spiritually connected to.</description>
      <author>Judy and Dayna</author>
      <pubDate>Fri, 18 Sep 2009 23:50:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>Julie Michaels -- who was in some movies with Patrick Swayze -- created a tribute page for him on caring.com:

http://www.caring.com/caring-candles/cancer-candle/in-honor-of-patrick-swayze-6/thejewels</description>
      <author>Tim</author>
      <pubDate>Fri, 18 Sep 2009 22:31:01 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>I have a life-threatening cancer. I am also a journalist who chooses words carefully. I 'deal' with a chronic illness, I do not 'fight' or 'battle' it, terms the writer repeatedly used. Do we use the same terms used in war for other chronic diseases, such as heart, diabetes, MS etc? And if we do, we shouldn't. I believe people who understand the birth-life-death cycle deal with illnesses as they go about living and ultimately dying. We don't battle life and unless we're egotistical and vai, generally do not fight against the inevitable. One might say life is a battle, and for some, it is even if they do not have cancer. It is unfortunate Swayze and many others die from cancer; it may eventually kill me. But I don't want my obituary to read that 'he put up a valiant battle' or 'put up the good fight' against an illness I did not ask for cancer, I did not do anything to get it, and I am resolved to deal with it - and get to on with life. And I keep a close eye for the inattentive drunk driver or one who is texting or talking on their cell phone and crosses the center line into my lane of traffic. I find these greater threats to my life than dying from cancer or any complications. </description>
      <author>Chuck Kershner</author>
      <pubDate>Fri, 18 Sep 2009 22:22:06 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>I have a life-threatening cancer. I am also a journalist who chooses words carefully. I 'deal' with a chronic illness, I do not 'fight' or 'battle' it, terms the writer repeatedly used. Do we use the same terms used in war for other chronic diseases, such as heart, diabetes, MS etc? And if we do, we shouldn't. I believe people who understand the birth-life-death cycle deal with illnesses as they go about living and ultimately dying. We don't battle life and unless were egotistical and vai, generally do not fight against the inevitable. One might say life is a battle, and for some, it is even if they do not have cancer. It is unfortunate Swayze and many others die from cancer; it may eventually kill me. But I don't want my obituary to read that 'he put up a valiant battle' or 'put up the good fight' against an illness I did not ask for cancer, I did not do anything to get it, and I am resolved to deal with it - and get to on with life. And I keep a close eye for the inattentive drunk driver or one who is texting or talking on their cell phone and crosses the center line into my lane of traffic. I find these greater threats to my life thn dying from cancer or any complications. </description>
      <author>Chuck Kershner</author>
      <pubDate>Fri, 18 Sep 2009 22:20:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>Lisa
I am soooo sorry about Patrick  :(  Stay Strong and keep the faith!
Pamela Tucker</description>
      <author>angeleyes Blue</author>
      <pubDate>Fri, 18 Sep 2009 21:16:40 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>My sympathies to you, Lesa, your husband was a beyond words actor and dancer.  In listening to reports of his health, I believe firmly that his stamina and state of healthy mind, and diet had alot to do with his living 20 months past diagnosis.  What people do not realize, is that the norm is 6 months or LESS.  Patrick was born a fighter and he never gave up.  I heard about the cookout with friends just shortly ago and wish I had been able to express my gratitude in person.  Thank you Patrick for being an inspiration to all of us and I am grateful for God placing you in this world.  And, for others who have cancer, take your inspiration from Patrick, work towards getting Congress to give funding and work your fight, never give up, never surrender.</description>
      <author>Anonymous</author>
      <pubDate>Fri, 18 Sep 2009 21:03:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Compassion Fatigue: To Stop Caregiving Stress, Stop Caregiving</title>
      <description>PT Cruzr, you bring up a great question on how do we let our parents know we need the break, which I'm going to add to our Family Advisor Carol O'Dell's long queue of family conflict questions. Thanks for sharing your story -- I hope you know it's good to vent! Plus you bring up a lot of points that will help others in similar shoes.</description>
      <author>Paula Spencer</author>
      <pubDate>Fri, 18 Sep 2009 18:09:57 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/compassion-fatigue</guid>
      <link>http://www.caring.com/blogs/compassion-fatigue/comments</link>
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      <title>Comment on Compassion Fatigue: To Stop Caregiving Stress, Stop Caregiving</title>
      <description>I had a near mental type breakdown earlier this month when my sister told me that she would be gone for the next 8 weekends and would during that time also be taking 2 weeks vacation.  My mom lives with my sister and my sister works full time.  I take mom on all of her appointments, take her one night a week for dinner and cover for my sister when she is gone on vacation (which she tries to do once per month) but giving up 8 weekends in a row without my husband almost put me over the edge.  I work every other weekend so my weekends are my getaway too.  I have been caring for my parents now for 8 years.  My father died 3 years ago and my mom moved in with my sister 2 years ago.  I have taken care of all of their appointments during this time and while mom never lived with me, many weeks, I spend at least 3 days with her and one evening.  And when Dad was alive he had to go to the hospital 2-3 times a week. (And I was the cab)
So, while my sister was continuing to get away, I wasn't and it got to me.  After I nearly fell apart, we enlisted the help of my daughter and my niece for the weekends (I will still take care of mom for the week when my sister is gone) but you cannot believe what a difference this made.  I still see mom at least 3 days a week but I needed to take a day to NOT WORRY about her.  
I will be going away next week for 3 days...the first vacation all year and I am looking so forward to it.  
I also found that one weekend, I had my daughter take care of mom and I tried desperately to keep from phoning mom and that getaway helped immensely.  We all need to just NOT WORRY for a time.  
I cannot imagine trying to care for a parent without having someone to share it with.  
One of our biggest problems with mom is the guilt that she puts on us when we want to get away.  Immediately when my sister says that she is going to be away, Mom says she will come to stay with me.  She makes my sister feel guilty for being gone all the time and when I told her I was going away for 3 days, maybe her &quot;heart is failing&quot;.  How do you make the parent know that you need to get away so you can be a better person for them?
Oh, and by the way, during these mini-vacations for my sister, we hired a home care provider for one night and mom said that she was weird, my daughter was unreliable,etc., etc.  She is only happy with her daughters and we can't be there all the time.  
Sorry for being so long winded...just need to vent.  I believe that communication is very important in these situations and we all need to remember that we still love our parents and when they are gone, you know how much you love them and you can't get them back.  </description>
      <author>PT Cruzr</author>
      <pubDate>Fri, 18 Sep 2009 13:51:53 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/compassion-fatigue</guid>
      <link>http://www.caring.com/blogs/compassion-fatigue/comments</link>
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      <title>Comment on World Alzheimer's Day and Why People With Alzheimer's Need It</title>
      <description>It is important for patients and families affected by diseases such as Alzheimer&#8217;s to consider participating in clinical studies.  One such study is the ICARA Study (www.icarastudy.com), whose goal is to explore if an investigational drug, called Bapineuzumab, can help slow the progression of Alzheimer&#8217;s Disease.  Clinical studies that test new treatments are the best chance we have for fighting this disease.  Current therapies for Alzheimer&#8217;s treat the symptoms associated with it, not the disease itself.</description>
      <author>Laura_ICARAStudy</author>
      <pubDate>Thu, 17 Sep 2009 20:48:30 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/world-alzheimers-day</guid>
      <link>http://www.caring.com/blogs/world-alzheimers-day/comments</link>
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      <title>Comment on World Alzheimer's Day and Why People With Alzheimer's Need It</title>
      <description>this is a devastating disease, for the patient and their families. you lose your loved one long before they die. my mother had dementia a form of alzheimer's, i lost her 3 months ago to the day. she suffered for a good 7 yrs. I was her only care taker, i finally had to put her in a convelesant home , she needed 24 hr care and i couldn't do it by myself. i visited her everyday, i miss her so bad. so my suggestion is talk, remonise, laugh, love and spend as much time with your loved one before they forget who you are.i held my mom's hand until she died, i was so sorry i couldn't help her, but now she's in heaven and at peace. she's my guardian angel now.</description>
      <author>serioussue</author>
      <pubDate>Thu, 17 Sep 2009 14:39:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/world-alzheimers-day</guid>
      <link>http://www.caring.com/blogs/world-alzheimers-day/comments</link>
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      <title>Comment on Compassion Fatigue: To Stop Caregiving Stress, Stop Caregiving</title>
      <description>Great article Paula,

Caregiver stress is a serious issue and a difficult one to broach. But it is important for each of us to realize that we only have so much to give. That we need to take care of ourselves. In the long run, taking a break and breaking the stress is better for the care recipient too.

I liked your suggestion on looking locally for a friend or family member and you suggestion of hiring a care provider. I saw, maybe you can combine the two. Many adult children live far from their aging parents leaving just one sibling to care for mom or dad. Maybe ask those living far away to pitch in for hired care that you can trust. Just a thought.

For more information on eldercare, check out our blog at http://www.rightathome.net/seniorhomecare.</description>
      <author>RightatHome</author>
      <pubDate>Thu, 17 Sep 2009 14:39:00 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/compassion-fatigue</guid>
      <link>http://www.caring.com/blogs/compassion-fatigue/comments</link>
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      <title>Comment on World Alzheimer's Day and Why People With Alzheimer's Need It</title>
      <description>I want the world to know
1. this disease is awful
2. this disease shouldnt be wished on your worst enemy
3. this disease needs a cure.</description>
      <author>Anonymous</author>
      <pubDate>Wed, 16 Sep 2009 23:44:13 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/world-alzheimers-day</guid>
      <link>http://www.caring.com/blogs/world-alzheimers-day/comments</link>
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      <title>Comment on Health Risks from Drinking Soda, Especially for Women</title>
      <description>This is complicated stuff, and researchers have not been able to conclusively say exactly how cola drinking is causing bone loss. Caffeine is partly reponsible, but studies have found problems with non-caffeinated colas as well. Some researchers believe the phosphoric acid interacts in a way that leaches calcium. See this medical article for more information. http://www.medpagetoday.com/Endocrinology/Osteoporosis/4247</description>
      <author>Melanie Haiken</author>
      <pubDate>Wed, 16 Sep 2009 23:26:26 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/soda-health-risks</guid>
      <link>http://www.caring.com/blogs/soda-health-risks/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>I agree with the comment above, I to had cancer, which at this stage has been told by my doctor that it was taking out and I would not need chemo or radiation.  I am very glad about that.  With prayers from family, friends and even strangers, I feel this has helped.  I have continued to feel stronger and more more like my old self.  We need to make the government more aware of natural ways of dealing with this horrendous disease.  My God bless those with this serious sickness.  My Prayers.</description>
      <author>greendeere40</author>
      <pubDate>Wed, 16 Sep 2009 21:15:57 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Patrick Swayze's Last Wish</title>
      <description>Many prayers to his family. what an awesome attitude to maintain during his struggle...I can relate and know too well that a positive attitude is extremely important. My doctors, radiation team, etc. encourage just that...so as he sais &quot;Keep Up the Fight&quot;, and believe in the guardian angels (soldiers) or whatever works for you. God Bless everyone with any form of cancer and also help the family, friends, and loved ones because I believe they too suffer and quite possibly more so emotionally etc. just watching this disease work its' horrors on their loved one.

Prayers to all!</description>
      <author>Anonymous</author>
      <pubDate>Wed, 16 Sep 2009 17:45:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/patrick-swayze-last-words</guid>
      <link>http://www.caring.com/blogs/patrick-swayze-last-words/comments</link>
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      <title>Comment on Dementia and Pain: How to Assess When Someone Hurts and Needs Help</title>
      <description>Thanks nursefluffers</description>
      <author>lmarie</author>
      <pubDate>Wed, 16 Sep 2009 12:08:54 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-and-pain</guid>
      <link>http://www.caring.com/blogs/dementia-and-pain/comments</link>
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      <title>Comment on Dementia and Pain: How to Assess When Someone Hurts and Needs Help</title>
      <description>this is excellent, I am sharing this with co-workers! </description>
      <author>nursefluffers</author>
      <pubDate>Tue, 15 Sep 2009 21:50:13 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-and-pain</guid>
      <link>http://www.caring.com/blogs/dementia-and-pain/comments</link>
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      <title>Comment on Health Risks from Drinking Soda, Especially for Women</title>
      <description>What does Octoman mean by &quot;heath an great compection&quot; when referring to what Joan Collins said? Also Is it Carbonic acid or Phosphoroc acid. It's unconscionable not to clarify this. </description>
      <author>ERP</author>
      <pubDate>Tue, 15 Sep 2009 21:41:49 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/soda-health-risks</guid>
      <link>http://www.caring.com/blogs/soda-health-risks/comments</link>
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      <title>Comment on What Is Someone With Dementia Thinking?</title>
      <description>My husband is now in very late stage dementia and is beginning end of life transition.  I can tell, because sometimes he is looking &quot;through me&quot; or over my shoulder at something else.  He is content there and might carry on a happy conversation.  Other times he looks right at me and smiles and tries to answer my questions.  He even tried to watch the tennis open as I carried on a happy conversation of what was happening. Believe when I tell you, they are still in there and reachable by your loving touch and words.  Remember, hearing is the last thing to go.</description>
      <author>Joy Golliver</author>
      <pubDate>Tue, 15 Sep 2009 19:52:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/mental-thinking-with-dementia</guid>
      <link>http://www.caring.com/blogs/mental-thinking-with-dementia/comments</link>
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      <title>Comment on Free Caregiving Help -- From Your Job?!</title>
      <description>WHat is an HR rep?</description>
      <author>Anonymous</author>
      <pubDate>Tue, 15 Sep 2009 14:22:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/free-help-for-caregivers</guid>
      <link>http://www.caring.com/blogs/free-help-for-caregivers/comments</link>
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      <title>Comment on Health Risks from Drinking Soda, Especially for Women</title>
      <description>Here I am poking my nose in again.
Joan Collins.said she put her good heath an great compection partly down to not drinking fizzy type drinks.</description>
      <author>octoman</author>
      <pubDate>Tue, 15 Sep 2009 14:00:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/soda-health-risks</guid>
      <link>http://www.caring.com/blogs/soda-health-risks/comments</link>
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      <title>Comment on Health Risks from Drinking Soda, Especially for Women</title>
      <description>Hi
I discovered that my habit of drinking large amounts of colas may have been contributing to bladder problems. Essentially, if I sneezed I had to stop walking or moving and pray that I didn't sneeze again because my bladder would seem to &quot;let go&quot;. Well, my doctor said that a number of her other female patients who complained of the same issue seemed to have a similar habit....drinking lots of colas. She said it seemed to provide significant relief when they cut back dramatically or ceased drinking colas. So I gave it a shot and completely cut out the cola drinks for one week. And guess what?  My whole problem ceased immediately (this had been going on for years!). I started back drinking colas and tried to note about how much I was drinking per day when the problem started up again. So I sorta figured out how much I could drink and not have this problem.  I can always tell when I overdo the cola's. It is a hard habit to break. I also noticed that if you leave a cola drink in a paper cup over night, that it essentially eats the paper up - just destroys it! I can only imagine what it must do to sensitive tissues in the human body.  In spite of this, I still drink too much. But I have cut back considerably thanks to my doctor noting this pattern with her patients.</description>
      <author>pollytnjc</author>
      <pubDate>Tue, 15 Sep 2009 13:40:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/soda-health-risks</guid>
      <link>http://www.caring.com/blogs/soda-health-risks/comments</link>
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      <title>Comment on Why People With Dementia Need Daily Exercise</title>
      <description>I also read a very good 5 Top things you can do to protect your Memory.

 Top 5 things you can do to Protect your Memory


1) Avoid Neurotoxins
Neurotoxins are very damaging to the brain, a specific group called excitotoxins actually engages your brain cells and can over stimulate them to the point your brain cells begin to die due to the hyper activity.

2) Fitness &amp; Exercise - Moderate exercise is key!
Studies have shown moderate exercise on a frequent basis can improve your overall memory and recall

3) Take Neuralox daily.
The brain is vital to our existence and quality of life, why not protect it from harm. Neuralox Triple action formula protects the mind, nourishes the brain, and enhances your memory. Take Neuralox Advanced Memory Formula - Try Risk Free for 21 days.
www.neuralox.com

4) Life Style, Quit Smoking,Avoid Drug and Alcohol abuse
Quit Smoking
Research published in the American Journal of Public Health shows that smokers over the age of 40 have a much faster rate of memory loss than non-smokers.
Avoid Drug use
Studies have long shown the connection of pot smoking (marijuana) with impairment of memory function. Now even more brain damaging drugs are prevalent such as Ecstasy or more commonly known as &#8220;E&#8221;. Studies have shown that memory function can be permanently impaired by MDMA, the active ingredient in &#8220;E&#8221;.
Alcohol Abuse
Alcohol abuse is a serious condition for many reasons. One reason is that alcohol abuse can lead to several types of memory loss. Alcohol has significant impact on the brain's ability to make and retain memories.

5) Exercise for the brain
This concept is really starting to take off as there are more and more products to stimulate the brain in the form of online games and computer based puzzles. Without getting into the technical how, simply the more you use your brain the better trained it is to function.
</description>
      <author>310Al</author>
      <pubDate>Tue, 15 Sep 2009 01:31:04 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/exercise-and-dementia</guid>
      <link>http://www.caring.com/blogs/exercise-and-dementia/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>The hard part about caregiving is that the system I turned to (The Legal system) to get some relief is as much of a problem as my siblings. 
My Sisters who live out of stste came home took my Mother from our home in my absents and had her to put their name on her bank account as joint owners and to sigh the family property to them. dropped her of and went back to their homes. There are seven of us and I found out about the transastion when check started to bounce and the taxes appeared in the paper as past due
So I turned to the legal system to get guardianship my mistake was in my choice of Attorneys. Not filing documents in a timely manner not serving all parties missing deadlines. In the mean time my sibling are not speakin to me and I am alone in my caring for my mother. Because of the recent transfer of property, the services that is available is not and the money that was in the bank, was transffered to my sisters accounts. One sister used the money to pay for Lapband surgery and to take a cruise. The other sibling are not available one brother passes by almost daily but do not stop. The other brother calls my phone and ask how is your mother doing. When I informed him that It is also his mother he made the comment you are the one who went to court so you got it all under control. It is my extended family who I can call on and depend on to support me and to help out.  </description>
      <author>peach11</author>
      <pubDate>Mon, 14 Sep 2009 06:08:05 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on Health Risks from Drinking Soda, Especially for Women</title>
      <description>Carbonated beverages contain carbonic acid, not phosphoric acid to create the fizz.  Some have extremely minute amounts of phosphoric acid in them to stabilize color.  Carbonic acid breaks down to carbon dioxide and water when the pressure is released to create the fizz so it cannot get into the blood stream.  Tooth hazard yes, bone hazard, no.
I fudmongering.</description>
      <author>MercTech</author>
      <pubDate>Mon, 14 Sep 2009 04:36:16 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/soda-health-risks</guid>
      <link>http://www.caring.com/blogs/soda-health-risks/comments</link>
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      <title>Comment on What To Do When a Family Disagreement Makes Caregiving Way Harder Than It Needs To Be</title>
      <description>Elder care mediators have a specialized process knowledge base and understanding of the life changing issues faced by elders and their families. They assist in navigating the uncertain path created by unplanned changes in the physical, emotional, and relational well being of parents.

Elder care mediator&#8217;s are focused on serving the elders and the families through offering a process that creates a safe space for an often difficult dialogue.

Your elder care mediator should NOT be a caregiver or your care manager. Elder care mediators (and mediators in general) are always neutral parties.

Look on the local link on this site and search for mediators. Also conduct a county or city internet search under the keywords &quot;elder care mediation in _____ county and (state)&quot; This should lead you to local resources. Be certain you find a mediator with a specialization in elder care/gerontology! For example, Accordo Mediation Specialists, LLC has elder care specialists who are certified mediators through their elder care division.</description>
      <author>accordo</author>
      <pubDate>Sun, 13 Sep 2009 22:27:34 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be</guid>
      <link>http://www.caring.com/blogs/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be/comments</link>
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      <title>Comment on Federal Initiative Brings Nursing Home Patients Home</title>
      <description>This site is just like all the rest no real answers to real questions!</description>
      <author>godhelpme</author>
      <pubDate>Sat, 12 Sep 2009 07:25:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/federal-initiative-brings-nursing-home-patients-home</guid>
      <link>http://www.caring.com/blogs/federal-initiative-brings-nursing-home-patients-home/comments</link>
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      <title>Comment on Grandparent's Day (or Any Day) Gifts Kids Can Make</title>
      <description>i like that these ideas are fast and easy, most of them</description>
      <author>Anonymous</author>
      <pubDate>Fri, 11 Sep 2009 18:38:39 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/grandparents-day-gifts</guid>
      <link>http://www.caring.com/blogs/grandparents-day-gifts/comments</link>
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      <title>Comment on Financial Crises for Caregivers: The Time vs. Money Dilemma</title>
      <description>OMG!!!  This didn't even answer the question!!!  The question is, how do I keep my job, health insurance, income, house, sanity!!!  Clip coupons and get utility discounts.  Honestly.  This is a serious question, not one that deserves half-brained suggestions like these.  My husband was the one that was ill, so I am the only income.  What I had to do was just work as much and as hard as I could when I was able and pray that my boss didn't get tired of it and let me go.  I was lucky in that I have teenagers that could stay with him several hours a day while I worked.  There really isn't much help for us, I have found, so even having gone through it, I have no suggestion other than hard work, and prayer.</description>
      <author></author>
      <pubDate>Thu, 10 Sep 2009 03:56:42 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/financial-crises-for-caregivers-the-time-vs-money-dilemma</guid>
      <link>http://www.caring.com/blogs/financial-crises-for-caregivers-the-time-vs-money-dilemma/comments</link>
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      <title>Comment on Prescription Addiction Part 2: (Grand)Mother's Little Helpers</title>
      <description>My mother was given Lortab after surgery for a broken hip, that was in May of 07 and by July 07 she was still on them per Dr's orders, why I don't know.  The surgery was healed and all she had was back pain from scoliosis for which she had never taken pain medication. I went round and round with them about it, I wanted the dosage reduced to help get her off of them; her personality changed and she seemed to be in more pain when she was on them between her &quot;fixes&quot; On top of that she was on a laxative and 2 stool softeners and was so constipated she had to dig it out with her finger.  She was losing weight and so they had her take Ensure and she had 2 seizures in a row.  She had never been on any type of medication and hadn't even taken an aspirin in over 20 years so I started looking at the medications.  One of the stool softeners can cause seizures in people prone to them.  So using that as my leverage I told the Dr I wanted her off of the Lortab because it was causing the constipation and all the laxatives too.  They told me she would get an obstructed bowel.  I told them I knew what to do for the constipation.  I went to the store and bought her prunes, cashew nuts and yogurt, she had a bowel movement the next day and no more seizures.  She was in the hospital a year later for pain in her bladder which turned out to be too much calcium it was blocking her urethra from the Caltrate she was taking, I put her on liquid calcium and give her cranberry for UA health.  They found out she needed a pacemaker and put her on Prolosec like the first time and wanted to give her Lortab and all the laxatives again and I told them no.  I went out to the nurses desk and told everybody sitting there what I just typed here and when I came back to the hospital the next day she had 2 armbands on NO Opiates, No stool softeners or laxatives.  We had no problems and she has been fine ever since.  My husband was in the hospital and was taking the highest dose of Lortab and they wouldn't let him leave until he had a bowel movement, I went to the grocery store and bought a six pack of Texun Ruby Red Grapefruit juice and he drank a couple of cans of that and had a bowel movement and then worked to get off of the Lortab, he's not on any pain medication no. They were both so grouchy and hateful until they got off the meds all together and they are normally very kind and loving.  I can't take Lortabs, I'm allergic to them.  It just seems that organized medicine wants to put you on drugs and keep you on them.  I believe our food is our medicine and if you eat well you won't need the drugs, that is the approach I use for my family.  </description>
      <author>CHICA60</author>
      <pubDate>Wed, 09 Sep 2009 22:04:05 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/prescription-addiction-among-seniors</guid>
      <link>http://www.caring.com/blogs/prescription-addiction-among-seniors/comments</link>
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      <title>Comment on Financial Crises for Caregivers: The Time vs. Money Dilemma</title>
      <description>give them the phone number to the nursing home and place your # on the do not call list.</description>
      <author>Anonymous</author>
      <pubDate>Wed, 09 Sep 2009 19:18:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/financial-crises-for-caregivers-the-time-vs-money-dilemma</guid>
      <link>http://www.caring.com/blogs/financial-crises-for-caregivers-the-time-vs-money-dilemma/comments</link>
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      <title>Comment on Financial Crises for Caregivers: The Time vs. Money Dilemma</title>
      <description>This article was not helpful - and worse, implies that it contains some information that caregivers can use.  Especially irksome was the line about a reply to Meigsters question being a helpful answer....drum roll please!  After going to that link the &quot;helpful&quot; info was to check with your state because *some states let you be PCA*.  DUH DUH DUH DUH DUH!!!
WHen will editors and writers realize that most caregivers have spent so much time looking for info, unless it is something real please don't pull our chains and get our hopes up.  Saving receipts and asking grandma to help with the bills is not helpful..,....recognizing that care for an elder family member is costly, takes time, and impacts your finances is helpful.  No more articles like this please.  We deserve better as caregivers, please respect our time when writing do nothing articles like this</description>
      <author>Anonymous</author>
      <pubDate>Wed, 09 Sep 2009 19:17:23 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/financial-crises-for-caregivers-the-time-vs-money-dilemma</guid>
      <link>http://www.caring.com/blogs/financial-crises-for-caregivers-the-time-vs-money-dilemma/comments</link>
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      <title>Comment on Can Marilyn Monroe or George Clooney Predict Alzheimer's?</title>
      <description>Now you see my memory problem I misspelt remember
in my blog,yes I can spell it.but I didn't also I did not notice this until posted it,then it was like a sore thumb.Freudian?may be.
My mother had alzheimer's but I think being 79 may have something to do with it.I forgot Marilyn Monroe's name After watching Bus Stop.why?
I remember dreams some people dont.but my dreams have meaning.I was on Richard Dawkins website I queried their belief that we all came from one cell They called me all sorts of an idiot .The website was red hot.that night I had a dream,my neighbour had dumped all his rubbish in my garden,symbolic?it was to me.</description>
      <author>octoman</author>
      <pubDate>Wed, 09 Sep 2009 17:37:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/predicting-alzheimers</guid>
      <link>http://www.caring.com/blogs/predicting-alzheimers/comments</link>
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      <title>Comment on Tips to Help Family Caregivers Save Both Time and Money</title>
      <description>My husband has Alzheimers and can't travel alone. It would be so helpful if the bus service that comes to the house did not charge for the assistance, but when you have to pay 2.50 for each of you going and then 2.50 each coming home, that is $10.00 for transportation to the doctor (or wherever).The service would be great, but it is just too expensive for us.</description>
      <author>1care</author>
      <pubDate>Wed, 09 Sep 2009 17:03:57 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-tips</guid>
      <link>http://www.caring.com/blogs/caregiver-tips/comments</link>
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      <title>Comment on Can Marilyn Monroe or George Clooney Predict Alzheimer's?</title>
      <description>I am sorry It is a spectacular approach to a normal human funtion memory loss.
Strange  we can rembember some names and not others some film stars and not others ,I have a simple way of over coming this problem.
I have ninety golfing friends names to remember every week.
I just imagine crown on the head of George a potty on the head of Jerry A leg of mutton on Jeffs head .  long  John big Fred and a I never have trouble again,sort of giving my memory a clue.   </description>
      <author>octoman</author>
      <pubDate>Wed, 09 Sep 2009 17:03:34 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/predicting-alzheimers</guid>
      <link>http://www.caring.com/blogs/predicting-alzheimers/comments</link>
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      <title>Comment on Free Caregiving Help -- From Your Job?!</title>
      <description>I am one of the fortunate that has an eldercare benefit.  My mother is 89 years of age and even though she is in assisted living, this benefit has certainly paid off for me. Frequent hospitalizations means that she goes back to assisted living with the need for a lot more assistance that is provided.
We get 20 days per year of eldercare and pay a co-pay of $40 per day of one on one care (during our scheduled working day(s). You can't beat that.
I would recommend that you contact your HR representative to look into this.</description>
      <author>Dino</author>
      <pubDate>Wed, 09 Sep 2009 13:45:46 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/free-help-for-caregivers</guid>
      <link>http://www.caring.com/blogs/free-help-for-caregivers/comments</link>
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      <title>Comment on An Aspirin a Day Keeps Colon Cancer at Bay</title>
      <description>On reading blog again 61% improvement  is deceptive
it does mean 60 patients in every 100 survived.
If only one person in a hundred without aspirin survived it means just over two people more people,survived with aspirin.
 50% would mean exactly two people survived.
The magic of maths,it could also mean at 79 I have gone Ga Ga and my maths have followed me.
 </description>
      <author>octoman</author>
      <pubDate>Wed, 09 Sep 2009 05:43:50 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/daily-aspirin-reduces-colon-cancer-risk</guid>
      <link>http://www.caring.com/blogs/daily-aspirin-reduces-colon-cancer-risk/comments</link>
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      <title>Comment on An Aspirin a Day Keeps Colon Cancer at Bay</title>
      <description>I used to take a aspirin a day until I was diagnosed with stomach cancer.
It did help,it caused my cancer to bleed more so  that I became acutely anemic.and they found my cancer earlier.
So aspirin may help but it can also harm.</description>
      <author>octoman</author>
      <pubDate>Wed, 09 Sep 2009 05:26:26 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/daily-aspirin-reduces-colon-cancer-risk</guid>
      <link>http://www.caring.com/blogs/daily-aspirin-reduces-colon-cancer-risk/comments</link>
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      <title>Comment on What Is Someone With Dementia Thinking?</title>
      <description>My mother has Alzheimer's and is 86 years old,  she thrives on social contact and her mood is much better when she visits relatives who live out of town. She loves when I visit and I tell her stories of when she and my aunts/uncles/grandma were young and when my family of origin were growing up.  She loves to hear them, of course, these are stories that she or my other relatives have passed on to me, but she loves to hear them because she can't remember them herself.  I tell her who I am, what day it is, and tell her the names of her family of origin, and then tell her the names of my brothers and sisters.  I also make sure that she is dressed appropriately for the weather and make sure she has eaten, is drinking enough water, and take her blood pressure to reassure her that she's OK.  She has had a TIA (mini-stroke) and a heart attack, so she worries alot when she doesn't feel well.  I really love my mother and now it's like I am the mother and she is my baby.
The article was spot on concerning the behavior and emotions of my mother.  It was a great article.

Thanks,
Eva Carvajal</description>
      <author>luckybabygirl</author>
      <pubDate>Tue, 08 Sep 2009 16:58:51 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/mental-thinking-with-dementia</guid>
      <link>http://www.caring.com/blogs/mental-thinking-with-dementia/comments</link>
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      <title>Comment on What Is Someone With Dementia Thinking?</title>
      <description>Informative and comforting.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 08 Sep 2009 13:54:13 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/mental-thinking-with-dementia</guid>
      <link>http://www.caring.com/blogs/mental-thinking-with-dementia/comments</link>
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      <title>Comment on What To Do When a Family Disagreement Makes Caregiving Way Harder Than It Needs To Be</title>
      <description>I am a caregiver by default and proximity for an 80 yr old roommate with two broken hips. He relies on me for everything except financial. He is hyper-critical, derides me, is adept at denying responsibility for his actions (I'm always the culprit) and has a ready excuse for being unable to cooperate with my &quot;badgering&quot; requests. IE, &quot;Could you please throw your wet clothes (incontinence)in the plastic pale rather than on the hardwood floors?&quot; &quot;Stop yelling at me!,&quot; is his usual response. His reactions to any efforts to reason have been to make an anti-Semitic remark, threats to call the police for &quot;harassing&quot; him and, most recently, the repetition of how much he hates me and his hope I will soon die (I have a brain tumor). A worker bathes him weekly. I prepare meals, shop, do laundry, take care of the dog. I've stopped talking to him because this seems the only way to avoid conflict. My one attempt to engage his social worker in a mediation process was a disaster. My roommate ranted that I had no &quot;rights&quot; to complain, that I was &quot;just a roommate&quot; and had overstepped my bounds. I'm at my wits end. </description>
      <author>boredwell</author>
      <pubDate>Mon, 07 Sep 2009 20:42:02 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be</guid>
      <link>http://www.caring.com/blogs/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be/comments</link>
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      <title>Comment on RIP, Ted Kennedy--and Thank You</title>
      <description>Thank you for this fine tribute.  He is loved.</description>
      <author></author>
      <pubDate>Sun, 06 Sep 2009 19:01:49 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/ted-kennedy-death</guid>
      <link>http://www.caring.com/blogs/ted-kennedy-death/comments</link>
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      <title>Comment on What To Do When a Family Disagreement Makes Caregiving Way Harder Than It Needs To Be</title>
      <description>Strange things happen with our Mother; hard of hearing, memory problems, quick changes from inability to co-operate in daily living chores to the opposite. Now that she has 3 caregivers the problems are more often than not. 15 yrs. difference in ages of daughters cause resentment issues in care decisions, tho all are educated in nursing to various degrees.  Blame goes from &quot; abuse&quot; to &quot;pampering&quot; on the different sides</description>
      <author>Anonymous</author>
      <pubDate>Sun, 06 Sep 2009 10:31:48 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be</guid>
      <link>http://www.caring.com/blogs/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be/comments</link>
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      <title>Comment on Are You About to Have A Heart Attack? 7 Heart Attack Signs Women -- And Doctors -- Often Miss</title>
      <description>I am 51, heart disease runs in my family. My dad died age 44. My brothers and I have all been on Cholestrol meds for a long time. I have had years of constant tightness in my chest. I had every heart test done and they tell me my heart is fine. They gave me Zanax to relieve my stress. I have had episodes of nausea, sweating, my arms tingle and my chest feels like someone is squeezing it but still they say it is all stress. I carry asprin with me and when this happens I chew a tablet. I have the constant fear I am going to have a heart attack and there is nothing I can do. Since losing my husband I am under a lot more stress but these symptoms have been going on for years. I am concered because my husband was not diagnosed early enough and when he was they told him you are going to die soon, he lasted 5 months and his life was over. Who can we trust? </description>
      <author>Dakota</author>
      <pubDate>Thu, 03 Sep 2009 15:47:06 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/signs-of-a-heart-attack-in-women</guid>
      <link>http://www.caring.com/blogs/signs-of-a-heart-attack-in-women/comments</link>
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      <title>Comment on 6 Ways to Work Around Someone Else's Denial</title>
      <description>Timely and thoughtful as always Paula! And such an important issue.  For myself, I think sometimes it leads to self-doubt.... maybe its me that's over reacting.  thanks!</description>
      <author>Rebecca</author>
      <pubDate>Thu, 03 Sep 2009 13:36:21 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dealing-with-denial</guid>
      <link>http://www.caring.com/blogs/dealing-with-denial/comments</link>
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      <title>Comment on Financial Crises for Caregivers: The Time vs. Money Dilemma</title>
      <description>Ihave taken care of our mother(3 other siblings--no financial help and very little otherwise) for 10 yrs. She had credit card debt when Itook over. I had been paying minimum until I recently had to put her in assisted living which they take all of her income. My name is not on her cards. Ido have power of attorney but am having trouble paying my own expenses. What needs to be done? I tell the creditors she is in a nursing home but they keep calling. Any suggestions?</description>
      <author>Anonymous</author>
      <pubDate>Thu, 03 Sep 2009 13:02:22 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/financial-crises-for-caregivers-the-time-vs-money-dilemma</guid>
      <link>http://www.caring.com/blogs/financial-crises-for-caregivers-the-time-vs-money-dilemma/comments</link>
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      <title>Comment on Tips to Help Family Caregivers Save Both Time and Money</title>
      <description>As a longtime caregiver I am disappointed that these typse of articles are still running.  The realities of caregiving are complex and are not one size fits all - to suggest that the senior &quot;take the bus&quot; or call a foodbank is ridiculous - Maybe they can take the bus to the foodbank and carry it all back with them.  I expected better.  Public transportation in most cities and suburban areas is subpar to unacceptable - in rural areas it does not exist.  Nutritional needs in seniors is pitted against food insecurity as prices rise and income falls - including the planned increase in Medicare Part B premiums at the same time that COLA (Cost of Living Increase) is not going to happen.  Please Caring.com ..... consider jettisoning the experts if this is the best they can do and ask real *at home* caregiving family members to contribute instead.  I look forward to learning new information, not looking at articles purporting to 'help' and hitting the delete key.  It is finally time for caregivers to speak up and ask for respect - not pie-in-the-sky articles like this.
No offense to the author, but I doubt that they have considered what I have written - I hope they take my and others comments to heart.</description>
      <author>Anonymous</author>
      <pubDate>Wed, 02 Sep 2009 20:46:25 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-tips</guid>
      <link>http://www.caring.com/blogs/caregiver-tips/comments</link>
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      <title>Comment on Tips to Help Family Caregivers Save Both Time and Money</title>
      <description>I do understand your point, and you're right, some of these would be impossible with dementia. But my mom was actually suffering from severe mental impairment and I was still able to set up some transportation solutions, including a public bus. But yes, she was stubborn, she did refuse, and I had to insist and explain patiently how impossible a burden it was for me to provide all transportation. Then she was willing to try. I should have mentioned that in any caregiving situation, a lot of back and forth has to go on to come up with a solution that works for everyone. </description>
      <author>Melanie Haiken</author>
      <pubDate>Wed, 02 Sep 2009 19:16:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-tips</guid>
      <link>http://www.caring.com/blogs/caregiver-tips/comments</link>
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      <title>Comment on Tips to Help Family Caregivers Save Both Time and Money</title>
      <description>So many of these suggestions are not doable. If the caregiver is aiding someone with dementia, early stage Alzheimers or just plain stubborn, giving them maps, cell phones and access to undependable senior transportation is useless. My mother was unable to use these as well as refused help from outsiders or spend money on services she was not familiar with. These tips may help those who have physical challenges but not mental ones.</description>
      <author>Anonymous</author>
      <pubDate>Wed, 02 Sep 2009 17:34:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-tips</guid>
      <link>http://www.caring.com/blogs/caregiver-tips/comments</link>
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      <title>Comment on Are You About to Have A Heart Attack? 7 Heart Attack Signs Women -- And Doctors -- Often Miss</title>
      <description>I have to say this scared the daylights out of me. I am a 31 year old female. I suffer from anxiety so I have every symptom that was mentioned. I am a health conscience person. I eat good, exersize and keep my weight down. If I have everyone of those symptoms, have been checked by a cardiologist and suffer from anxiety should I be rechecked???? </description>
      <author>ellkay</author>
      <pubDate>Wed, 02 Sep 2009 12:55:00 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/signs-of-a-heart-attack-in-women</guid>
      <link>http://www.caring.com/blogs/signs-of-a-heart-attack-in-women/comments</link>
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      <title>Comment on Can Marilyn Monroe or George Clooney Predict Alzheimer's?</title>
      <description>I agree with Friendma.  This type of testing is almost like playing &quot;Trivial Pursuit&quot;.... it is predicated on KNOWLEDGE of pop culture and current events rather than on actual brain FUNCTION.  Knowledge is self-controlled whereas brain function is not.  For a test such as this to be scientifically valid, it should be able to be duplicated.  How would you test someone from a different culture?  For example, Amish people live in our midst but they do not participate in our culture and would very likely not know the names of pop icons.  Like Friendma, I would not recognize many of the faces or names of some of the current heartthrobs, but, for now, my memory is fine.  I would label this as &quot;pseudo-science&quot; and is predictive of cultural participation, not purely brain function.  A better test would be to show random images and ask the participant to identify a specific type of object, such as a specific geometric shape.  Has this &quot;study&quot; been peer reviewed and held up to scientific scrutiny?</description>
      <author>mamoros</author>
      <pubDate>Tue, 01 Sep 2009 17:36:56 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/predicting-alzheimers</guid>
      <link>http://www.caring.com/blogs/predicting-alzheimers/comments</link>
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      <title>Comment on Testing for Your Genetic Risk of Alzheimer's: Yes or No?</title>
      <description>My adult children are facing this decision because my husband and his two sisters have Alzheimer's.  I do not recommend it to them until there is a cure or prevention drug.  I encourage good health.  I had breast cancer and there is a test for that as well, but no cure or treatment you could start.  So I don't recommend that to my daugther and neither did her doctor.  </description>
      <author>Anonymous</author>
      <pubDate>Tue, 01 Sep 2009 15:38:18 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/genetic-risk-of-alzheimers</guid>
      <link>http://www.caring.com/blogs/genetic-risk-of-alzheimers/comments</link>
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      <title>Comment on Can Marilyn Monroe or George Clooney Predict Alzheimer's?</title>
      <description>I don't have a memory problem but have never been a big movie fan or watched a lot of tv, so putting ME through that kind of test would most likely end up with an incorrect conclusion.  My husband couldn't have passed that test 25 years ago when he was healthy!  Einstein, probably...Monroe, maybe...Clooney or Spears...not a chance!  </description>
      <author>Friendma</author>
      <pubDate>Tue, 01 Sep 2009 15:08:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/predicting-alzheimers</guid>
      <link>http://www.caring.com/blogs/predicting-alzheimers/comments</link>
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      <title>Comment on RIP, Ted Kennedy--and Thank You</title>
      <description>Yes, there IS a question that he was an eloquent champion that would bring quality healthcare for all! A very serious question! The ramifications of his thinking on healthcare reform are tremendously frightening! Everyone would not receive the quality care we now know, nor would the best available care be given in a timely &amp;/or equitable way. I have relatives who are medical professionals in Canada and I have friends undergoing cancer treatment in Great Britain.  I'm very well aware of how things are done in those countries and Americans do not want to go that route.  The Ted Kennedy's of this world would have a certain quality of care for themselves, but would then determine what degree of &quot;quality&quot; care the rest of us could/should have and when we should have it.  Don't assume we all agree about what Ted Kennedy stood for. There is, after all, the &quot;controversy and legislative wrangling&quot; going on for a reason - people do not want this type of plan imposed on them.  They know a disaster when they see it.</description>
      <author></author>
      <pubDate>Mon, 31 Aug 2009 21:33:44 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/ted-kennedy-death</guid>
      <link>http://www.caring.com/blogs/ted-kennedy-death/comments</link>
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      <title>Comment on 10 Ideas for Getting a Reluctant Person Checked for Alzheimer's</title>
      <description>My husband was adamantly against home care, nursing homes, assisted living...just wanted to be at home with me.  To get him into the A/L facility, our doctor recommended that he check into a clinic for memory evaluation/assessment and hubby went without question.  However, after being there awhile, he still questions why he needs the &quot;testing&quot; and wants to come home. It hurt me to use the &quot;loving manipulation&quot; someone else suggested, but it was the only way.  He's getting the care now that I no longer can provide. </description>
      <author>Friendma</author>
      <pubDate>Mon, 31 Aug 2009 20:49:21 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/10-ideas-for-getting-a-reluctant-person-checked-for-alzheimers</guid>
      <link>http://www.caring.com/blogs/10-ideas-for-getting-a-reluctant-person-checked-for-alzheimers/comments</link>
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      <title>Comment on The 5 REAL Reasons You're Stressed &#8211;- and How to Tame Them Now</title>
      <description>It is easy to read about it but to take and put into real life situations for me is hard. I not only have my family to take care of I need to help my mom take care of my dad. 
I have had depression for over 16 years and don't know how to stop the feelings. When something hurts me instead of taking out on the person or thing that hurts me I take it out on myself. I am in couseling for it but i don't want to have to take medication for it. So I don't know what else to do.</description>
      <author>AlwaysDaddy'sGirl</author>
      <pubDate>Sun, 30 Aug 2009 20:17:29 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/stress-causes</guid>
      <link>http://www.caring.com/blogs/stress-causes/comments</link>
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      <title>Comment on The 5 REAL Reasons You're Stressed &#8211;- and How to Tame Them Now</title>
      <description>Terrific article, great reminders. Most of them break down to taking a &quot;left turn&quot; off of how I usually think &amp; operate. Guess it's good advice for dealing with life in general.</description>
      <author>jpirron1</author>
      <pubDate>Sun, 30 Aug 2009 12:46:47 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/stress-causes</guid>
      <link>http://www.caring.com/blogs/stress-causes/comments</link>
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      <title>Comment on The 5 REAL Reasons You're Stressed &#8211;- and How to Tame Them Now</title>
      <description>I pretty much know what you're sayin' &amp; try to do those things........still hard &amp; lack of options/help!</description>
      <author>Spockula</author>
      <pubDate>Sun, 30 Aug 2009 06:07:52 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/stress-causes</guid>
      <link>http://www.caring.com/blogs/stress-causes/comments</link>
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      <title>Comment on The 5 REAL Reasons You're Stressed &#8211;- and How to Tame Them Now</title>
      <description>Gosh can I relate to STRESS!  Been a rough year so far.  Hard to be upbeat.  Need prayers and a hug.</description>
      <author>sophie659</author>
      <pubDate>Sat, 29 Aug 2009 01:46:58 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/stress-causes</guid>
      <link>http://www.caring.com/blogs/stress-causes/comments</link>
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      <title>Comment on The 5 REAL Reasons You're Stressed &#8211;- and How to Tame Them Now</title>
      <description>No one can feel the way I have in the last year.
These and more apply...
I challenge anyone to go through what I've gone through without support!</description>
      <author>Anonymous</author>
      <pubDate>Sat, 29 Aug 2009 00:03:41 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/stress-causes</guid>
      <link>http://www.caring.com/blogs/stress-causes/comments</link>
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      <title>Comment on The 5 REAL Reasons You're Stressed &#8211;- and How to Tame Them Now</title>
      <description>#4 and #5 are definitely me right now!  Thanks for helping me see it...</description>
      <author>Slipjig</author>
      <pubDate>Fri, 28 Aug 2009 21:48:19 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/stress-causes</guid>
      <link>http://www.caring.com/blogs/stress-causes/comments</link>
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      <title>Comment on The 5 REAL Reasons You're Stressed &#8211;- and How to Tame Them Now</title>
      <description>Yes !!!  Very helpful......so many ways I am feeling right now !!!  sometimes we need to see it in writing to help us get on with life !!!   Thanks !!!  </description>
      <author></author>
      <pubDate>Fri, 28 Aug 2009 13:28:20 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/stress-causes</guid>
      <link>http://www.caring.com/blogs/stress-causes/comments</link>
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      <title>Comment on Are You About to Have A Heart Attack? 7 Heart Attack Signs Women -- And Doctors -- Often Miss</title>
      <description>women, please listen to your body! I am a registered nurse and had everyone of these symptoms but blew them off as change fo life till one day I hooked myself up to the monitor and saw I was having irregular rythms called PVC's. I went to the cardiologist and had a stress test. The next day he came up on my unit sent me home said I was in heart failure!!!!!!I now have a pacemaker and defibrilator. I no longer allowed to work... so DONT ignor your symptoms or blow them off.</description>
      <author>Pattycakes</author>
      <pubDate>Fri, 28 Aug 2009 01:16:56 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/signs-of-a-heart-attack-in-women</guid>
      <link>http://www.caring.com/blogs/signs-of-a-heart-attack-in-women/comments</link>
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      <title>Comment on Are You About to Have A Heart Attack? 7 Heart Attack Signs Women -- And Doctors -- Often Miss</title>
      <description>I'm so happy to hear you found this post helpful. Yes, please do go see a doctor, and make sure she runs all possible tests. I was very shocked to see the statistics of how many women have heart attacks and don't get to the doctor until days later.</description>
      <author>Melanie Haiken</author>
      <pubDate>Thu, 27 Aug 2009 23:21:49 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/signs-of-a-heart-attack-in-women</guid>
      <link>http://www.caring.com/blogs/signs-of-a-heart-attack-in-women/comments</link>
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      <title>Comment on Are You About to Have A Heart Attack? 7 Heart Attack Signs Women -- And Doctors -- Often Miss</title>
      <description>Last Friday, I was at my neighbor's house for dinner, after dinner, I suddenly felt extrememly weak, dizzy, and couldn't walk.  I asked my neighbor to walk me home and since I have a history of panic disorder, we thought it was another panic attack.  But this felt different, I was not panicky, just kept feeling worse, weaker, pressure in the middle of my chest, shortness of breath, and unable to walk. My friend called 911 and the ambulance took me to the hospital.
A couple of days before this, I had extreme intestinal cramping, the kind that makes you want to lay on the floor and scream, the pain was so bad. For several months previous, I have had insomnia.
I also had the sensation at the time of the incident of feeling my blood pounding through my head and body; and a curious sensation of tingles along the top of my head.
I stayed overnight at the hospital because I am high risk, I am 53, smoke (yes, I know I need to stop), about 65 lbs overweight, have a family history of strokes/heart attacks, and have chronic pain due to an accident.  That same week, I was very upset due to the fact that a longtime friend of mine for 30 years (male) did not want to be my friend any longer. This upset me greatly.
At the hospital, they ran blood enzyme test to determine if I had had a heart attack, the results were negative.
I believe that this incident might have been a precursor to a heart attack/stroke.  I am scheduled for a stress test.
I have been taking my health for granted, but will change my habits for better health.
</description>
      <author>luckybabygirl</author>
      <pubDate>Thu, 27 Aug 2009 18:13:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/signs-of-a-heart-attack-in-women</guid>
      <link>http://www.caring.com/blogs/signs-of-a-heart-attack-in-women/comments</link>
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      <title>Comment on Are You About to Have A Heart Attack? 7 Heart Attack Signs Women -- And Doctors -- Often Miss</title>
      <description>thanks a lot. Great post. I am experiencing it right now.  I have to make a doctors appointment as soon as possible.</description>
      <author>marlan98b</author>
      <pubDate>Wed, 26 Aug 2009 23:33:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/signs-of-a-heart-attack-in-women</guid>
      <link>http://www.caring.com/blogs/signs-of-a-heart-attack-in-women/comments</link>
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      <title>Comment on Five Debt Triggers -- One Simple Solution</title>
      <description>Debt settlement helps when you are not able to repay your debt amount. I was struggling to repay my my debts and I took help of &lt;a href=&quot;http://www.freedomdebtreliefshop.com/&quot;&gt;Freedom Debt Relief&lt;/a&gt; to settle my debts.</description>
      <author>rchrdle</author>
      <pubDate>Wed, 26 Aug 2009 04:58:20 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/causes-of-debt</guid>
      <link>http://www.caring.com/blogs/causes-of-debt/comments</link>
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      <title>Comment on When Caregiving for Someone With Alzheimer's, Emotions Are All-Important</title>
      <description>Very helpful and very relevant article.  I can see the truth of the importance of emotions, both as a trigger for negative/hostile/frustrated behavior and for maintaining a positive and calm outlook in the dementia patient/parent.  Thank you for your insight.</description>
      <author></author>
      <pubDate>Tue, 25 Aug 2009 17:26:29 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/emotional-stability-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/emotional-stability-with-alzheimers/comments</link>
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      <title>Comment on De-Stressing End-of-Life Care NOW (Whatever Healthcare Reform Brings)</title>
      <description>Thank you so much for your article.  You explained it in such a way that felt your compassion for your parents.  I have written several articles that I'd like to share: http://www.examiner.com/x-20416-Virginia-Beach-Elder-Care-Examiner

We must help each other.  The reality is: Each one of us will either become a caregiver, or need to have someone care for us.  We cannot excape it!
Please live a posting on the site.
By the way, hospice helps not only the dying, but most especially the living family members.  I would not have made it without them.  </description>
      <author>cashew</author>
      <pubDate>Mon, 24 Aug 2009 22:20:10 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/de-stressing-end-of-life-care-for-caregivers-now-whatever-healthcare-reform-brings</guid>
      <link>http://www.caring.com/blogs/de-stressing-end-of-life-care-for-caregivers-now-whatever-healthcare-reform-brings/comments</link>
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      <title>Comment on How to Choose the Best Nursing Home: Look for a Nonprofit</title>
      <description>You're right, I neglected to mention that a home run by an individual or family is in a different situation than one owned by a public company (usually part of a chain) with shareholders who focus mainly on profit/loss. I should have made this distinction. Of course it all comes down to the quality of management and every home is going to be different, so readers, use our guidelines to choose the best home, making an evaluation based on our list of factors to consider.</description>
      <author>Melanie Haiken</author>
      <pubDate>Mon, 24 Aug 2009 18:44:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/choosing-best-nursing-home</guid>
      <link>http://www.caring.com/blogs/choosing-best-nursing-home/comments</link>
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      <title>Comment on De-Stressing End-of-Life Care NOW (Whatever Healthcare Reform Brings)</title>
      <description>FIRST OF ALL-REGARDING HEALTH CARE REFORM-BE SURE TO FOCUS ON FACT AND NOT RUMOR.  BE VERY CAUTIOUS NOT TO FALL PREY TO RUMOR AND MEDIA HYPE.  BEFORE YOU REACT, GET EVERY FACT!  Advance directives put the patient in control.  Be sure to not only have it in writing-have a conversation with those you have designated to speak on your behalf to ensure that they know what your wishes are.  Hospice philosphy can offer a beautiful experience to all. I too have &quot;done it both ways&quot; (i.e. lost loved ones tragically &amp; suddenly vs. under Hospice care.  I'll take Hospice any day!) Each of us will face death some day.  Why not make it loving, reflective,and appreciative of the human being you are caring for.</description>
      <author>Ruth S-Professional</author>
      <pubDate>Mon, 24 Aug 2009 13:04:44 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/de-stressing-end-of-life-care-for-caregivers-now-whatever-healthcare-reform-brings</guid>
      <link>http://www.caring.com/blogs/de-stressing-end-of-life-care-for-caregivers-now-whatever-healthcare-reform-brings/comments</link>
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      <title>Comment on Is This Alzheimer's Prevention Advice Worth Changing Your Life Over?</title>
      <description>Having a wonderful Mom and an equally wonderful Mom-in-law with Alz. I can appreciate ANY possible help in life style changes. Most of the recommended information such as excercise, eating more veggies, getting rest, socializing and pray and mediatation will help any life style to improve. Right????</description>
      <author>knighthouse</author>
      <pubDate>Sun, 23 Aug 2009 16:58:33 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alzheimers-studies</guid>
      <link>http://www.caring.com/blogs/alzheimers-studies/comments</link>
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      <title>Comment on De-Stressing End-of-Life Care NOW (Whatever Healthcare Reform Brings)</title>
      <description>Thanks for helping sort out things. Although I feel only those of us facing end of life issues sees this information. Looks like when nothing else would get the american public off the proverbial couch health care reform did and about time too.</description>
      <author>knighthouse</author>
      <pubDate>Sun, 23 Aug 2009 16:50:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/de-stressing-end-of-life-care-for-caregivers-now-whatever-healthcare-reform-brings</guid>
      <link>http://www.caring.com/blogs/de-stressing-end-of-life-care-for-caregivers-now-whatever-healthcare-reform-brings/comments</link>
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      <title>Comment on De-Stressing End-of-Life Care NOW (Whatever Healthcare Reform Brings)</title>
      <description>ms Mad Dog - I interpreted the comment a bit differently, to mean that real life is not similar to TV life. I don't think the implication was that nurses don't care or that one should not bother with CPR!! I believe the message was not to buy in to the hollywood representation of end-of-life, don't delay putting your wishes in writing and discussing your desires.</description>
      <author>John</author>
      <pubDate>Sun, 23 Aug 2009 10:23:14 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/de-stressing-end-of-life-care-for-caregivers-now-whatever-healthcare-reform-brings</guid>
      <link>http://www.caring.com/blogs/de-stressing-end-of-life-care-for-caregivers-now-whatever-healthcare-reform-brings/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>When more than one adult sibling is involved in overseeing the care and finances of an elderly parent, all rarely agree on everything.  In our society, we are so stressed and busy - everyone seems to feel others have more time or money to help, than they do.
  In some cases, elder siblings may be facing their own changes or financial reverses - so suddenly, the living parents assets start looking like readily available &quot;funds.&quot;  
   Due to the complicated dynamics of siblings, families, and past memories/perceptions - it seems best to pay for expert guidance and mediation from sources that are not &quot;family.&quot;  If you &quot;move on&quot; - but leave the parent's care in uncapable hands - the eventual outcome may be far worse than a few hours of family &quot;mediation&quot; or &quot;therapy.&quot; </description>
      <author>Anonymous</author>
      <pubDate>Sat, 22 Aug 2009 17:10:28 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on How to Choose the Best Nursing Home: Look for a Nonprofit</title>
      <description>This article is not necessarily true.  I have worked in a for-profit nursing home for almost three years.  We do not have share holders, we are owned by one person.  If I did not believe the residents were getting the best care, I would not work for the facility.  The only pressure ulcers (bed sores) we have in our facility(and there are very few), the residents have gotten while at the hospital, which we usually get healed up fairly quickly. We are fairly well staffed. There are usually about 7 residents per nurses aid on average.  We are also a skilled care facility (which means we have people there for therapy).  I see a lot of these people want to stay permanently, and sometimes they do.  Our facility is very old, so it is not that pretty and fancy, but we take very good care of them and try to make sure they have fun.  So, if your looking for a nursing home dont rule one out just because it is for profit, you could be doing your loved one a great disservice.  FYI we are located in New Carlisle Ohio.   </description>
      <author>tabidean</author>
      <pubDate>Sat, 22 Aug 2009 02:25:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/choosing-best-nursing-home</guid>
      <link>http://www.caring.com/blogs/choosing-best-nursing-home/comments</link>
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      <title>Comment on Bad News for Those with Spinal Compression Fractures; Popular Treatment May Not Work After All</title>
      <description>Oh! I saw the send a hug.I thought why not.so I pressed it .low and behold I got a hug.
Lucky me.</description>
      <author>octoman</author>
      <pubDate>Fri, 21 Aug 2009 19:30:03 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/compression-fractures</guid>
      <link>http://www.caring.com/blogs/compression-fractures/comments</link>
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      <title>Comment on Bad News for Those with Spinal Compression Fractures; Popular Treatment May Not Work After All</title>
      <description>My wife has osteoporosis.She has two replacement knee's but her back now troubles her.living in England all these treatments are free,but of course there are long queues.But the fact that doctors are looking into their proceedures in great news,they are usually so blinkered.</description>
      <author>octoman</author>
      <pubDate>Fri, 21 Aug 2009 19:25:52 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/compression-fractures</guid>
      <link>http://www.caring.com/blogs/compression-fractures/comments</link>
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      <title>Comment on De-Stressing End-of-Life Care NOW (Whatever Healthcare Reform Brings)</title>
      <description>So the percentage of 70 and over don't survive CPR, is it Nurse Sara who would decide because of age don't bother?? Heaven help us old folks because a lot of young people would go with the don't bother routine.</description>
      <author>msmaddog</author>
      <pubDate>Fri, 21 Aug 2009 18:06:14 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/de-stressing-end-of-life-care-for-caregivers-now-whatever-healthcare-reform-brings</guid>
      <link>http://www.caring.com/blogs/de-stressing-end-of-life-care-for-caregivers-now-whatever-healthcare-reform-brings/comments</link>
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      <title>Comment on A &quot;Perfect Mom,&quot; a Bottle of Vodka, and 8 Dead: Why We Must Learn to Recognize Alcoholism in Women</title>
      <description>I grew up in a very abusive household &amp; my father was also an alcoholic. I am the youngest of three I myself have suffered with a long term alcohol addiction, I thought there was no way out, it was just one big cycle. I have now overcome my addiction and I am no longer an alcoholic, if anyone is reading this and needs help and support I seriously recommend this site Healthwise Global  www.healthwise-global.com  which is fantastic for helping manage stress, the site does have a special program to help overcome alcohol addiction ( which I used), the man who started the site was himself and alcoholic.  I hope it helps any one who is reading this article.

</description>
      <author>sunnywho</author>
      <pubDate>Wed, 19 Aug 2009 14:15:51 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alcoholism-in-women</guid>
      <link>http://www.caring.com/blogs/alcoholism-in-women/comments</link>
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      <title>Comment on When Caregiving for Someone With Alzheimer's, Emotions Are All-Important</title>
      <description>An excellent article, and so true.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 18 Aug 2009 19:12:00 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/emotional-stability-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/emotional-stability-with-alzheimers/comments</link>
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      <title>Comment on When Caregiving for Someone With Alzheimer's, Emotions Are All-Important</title>
      <description>Not only was it helpful, it was beautiful.  It is a tool that I use and Bob's care partner Kathy uses regularly.  There is a wonderful T Shirt by Suzy.  View it here www.suzytoronto.com. It has a poem titled She With Healing Hands.  I recommend it as a gift for a caregiver.</description>
      <author>Joy Golliver</author>
      <pubDate>Tue, 18 Aug 2009 17:30:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/emotional-stability-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/emotional-stability-with-alzheimers/comments</link>
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      <title>Comment on Anti-Cancer Superfoods: Do They Really Work?</title>
      <description>I have tried to access the link to get the 10 anti-cancer superfoods.  My screen is only showing the first 5. How can I access the other 5. I greatly appreciate this article. Thanks for any and all assistance.</description>
      <author>sandstone</author>
      <pubDate>Tue, 18 Aug 2009 16:58:54 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/anti-cancer-foods</guid>
      <link>http://www.caring.com/blogs/anti-cancer-foods/comments</link>
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      <title>Comment on When Caregiving for Someone With Alzheimer's, Emotions Are All-Important</title>
      <description>I agree - have found that my mother responds best when the mood is lighter. She has told me she notices body language in other people, and gets embarrassed even tho she may not realize just what she has done. When I am asked the same question for the umpteenth time, I try to pause for a beat or two, and smile and just respond as if it is the first time. I try not to let my body language convey anything negative. It is hard, but I have found that my pausing for a moment helps both of us!  I also agree with the last point - my mother is fine when I answer her question as it is put, because whether it is applicable to the situation or not, she will forget it momentarily. In the meantime, however, I have given her a response that she understood, and haven't made her feel like an idiot in the process.  Pride is important, and tho it may not seem like it, they beat themselves up inside whenever they realize they've made a &quot;mistake&quot;...they feel unimportant and a burden even more. It is so frustrating for us, but imagine how frustrating to them!  My mother was always on top of everything, and now she isn't. She knows it too. And it hurts to see the look on her face when she realizes that she isn't tracking. Imagine yourself there - </description>
      <author>pollytnjc</author>
      <pubDate>Tue, 18 Aug 2009 15:12:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/emotional-stability-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/emotional-stability-with-alzheimers/comments</link>
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      <title>Comment on When Caregiving for Someone With Alzheimer's, Emotions Are All-Important</title>
      <description>This was really helpful and informative....</description>
      <author>Sherryaw</author>
      <pubDate>Tue, 18 Aug 2009 13:29:28 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/emotional-stability-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/emotional-stability-with-alzheimers/comments</link>
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      <title>Comment on The Secret Guilt of Caregivers</title>
      <description>  My husband who will be 59 in October 2009 has been unable to work for the last 15 years due to his first +MI.  Since then he has had two more MI'S, PulmonaryHypertension, Cardiac tampanode, COPD, Diabetes Militus-Insulin dependent, morbid obesity, utilitizates oxygen 24hours a day and bipap at night.  He had a ruptured diverticulitis and has a colostomy, neuropathy of leg and feet, arthristis, has a torn rotator cuff of the right shoulder, can only transfer from bed to chair with assistance, is prone to GI bleeds, has renal calculi which he has been passing stones for the las 7 years from however the risk is to high for surgery, is becoming increasingly confused, falling when he tries to ambulate as he forgets about his disabilties and on and on it goes.  As these problems have developed and worsend ove the last 10 years we have tried to adapt as each new symptom developes.
   I had been working fulltime as an LPN at our local hospital until a year ago when I fell and broke my left angle.  I was on crutches for 3 months and then returned to work full time.  In 4 weeks I fell again and had a fracture of my left ankle and compound fracture of left foot.  They were unable to do surgery as I was caring for my husband at home still so was sent home with frx boot, crutches and non-weight bearing to left foot.
   Our daughter came home for a week, however she left her husband and 7 year old twins at home which is a 2 hour drive so she headed back for home.  I am 57 years old which leaves us to young for many of the services available to either the younger or senior population.  While I was off work with the 2nd fracture I developed neuropathy of both legs/feet, hypertension and depression.  I have had a seizure disorder-etiology unknown since I was 6 years old.  It is controlled with medications however I do not drive because of it and now that my husband is so sick he is unable to drive.
   I returned to work after 4 months during which time our hospital was taken over by another facilty with all new administration and many changes in personnel policies.  I was called in for a meeting
with my new supervisor who was not going to as lenient with me if I needed to leave because of my husbands declining health.  
   My work records were always good and after working at this hospital for 32 years I had missed work for 6 weeks when I had my daughter 24 years ago, a total of 11 full days for my own illness at different times in those 32 years until I had fractured my ankles in the last year so I still had PTO hours which I had accumulated and not yet used all of them even with my time off over the last year.  
   I was given the option of quitting on my own or being fired because of missing work and leaving at times for emergencies for husband which would result in any where from 30 mintues to the remainder
of a day depending on his problem at the time.  Now that neither of us are working I have reluctently tried to get assistance with some of the daily issuse which come in dealing with caring for my husband at home.  I have never before asked for help because of my seizure disorder and the inability to drive from anyone except for family members. My husbands Dr's. are a 2 hour drive and his appointment becoming more frequent as he has become more ill.  We live in a rural town with no intown transportation let alone long distance transportation to doctors or hospitals.  
   It is almost to the place where I am going to have to place him in a nursing home to get the care he needs from his physicians.  Both of us are becoming more depressed trying to figure out where to turn next.  There are many agencies out there but our ages makes us to old or to young for most of these services.  I have been told to go on medicare/medicaid, you have paid for it all these years so use it.  We have always tried to plan for our older years and I really do not want to turn this all over in one lump sum and then have nothing to fall back on in later years.  
   I feel we are the forgotten generation.  I resent that they are making me beg for help when we have always tried to care for things ourselves.</description>
      <author>jatmy</author>
      <pubDate>Tue, 18 Aug 2009 00:06:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-guilt</guid>
      <link>http://www.caring.com/blogs/caregiver-guilt/comments</link>
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      <title>Comment on Surprising New Research: Is It Alzheimer's--or a Vision Problem?</title>
      <description>Your extra tips about mirrors and throw rugs in front of doors (both the pro and the con!) are bound to help others, thanks for sharing them. ps</description>
      <author>Paula Spencer</author>
      <pubDate>Sun, 16 Aug 2009 02:40:33 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/improving-vision-for-alzheimers</guid>
      <link>http://www.caring.com/blogs/improving-vision-for-alzheimers/comments</link>
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      <title>Comment on Oral Histories: Preserving Your Family's Stories</title>
      <description>My mother and I would sit outside (weather permitting), enjoying a cocktail and she would dictate her story while I keyboarded as fast as I could into my laptop. We didn't have enough time for all the stories, but important dates and times, courtship, early marriage, moving a lot has been preserved. 
My mother, age 85, died suddenly (isn't it always) in New Orleans 2005, we had just had my daughters wedding. We didn't get to share any last words but we had shared a lifetime over the five years she lived with me.</description>
      <author></author>
      <pubDate>Sat, 15 Aug 2009 20:43:22 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/oral-histories</guid>
      <link>http://www.caring.com/blogs/oral-histories/comments</link>
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      <title>Comment on What To Do When a Family Disagreement Makes Caregiving Way Harder Than It Needs To Be</title>
      <description>My husband was sick for about a year, before he passed. I had no support from his sibling and father.Since his death, I am not included in nothing. What should I do?</description>
      <author>Quincy</author>
      <pubDate>Sat, 15 Aug 2009 18:30:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be</guid>
      <link>http://www.caring.com/blogs/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>Thanks for this posting Paula. It helps to know we are not a lone and it is actually common. 
I'm also glad you brought up the point of no reconciliation. Sometimes it just is not possible. We've learned that DNA doesn't mean a whole lot if you do not have honesty, respect, trust and love. You are right, it is important to move on. </description>
      <author>Anonymous</author>
      <pubDate>Sat, 15 Aug 2009 15:55:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on The Secret Guilt of Caregivers</title>
      <description>Thanks for the reminder that guilt is normal.  The older my mother gets, the more guilt I feel.  I feel that I'm it and am in no way nearly enough but don't see a way to involve others at this time.
It is true...It takes a village to raise a child and it takes a village to sustain an elder.</description>
      <author>sugarbay</author>
      <pubDate>Sat, 15 Aug 2009 00:48:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-guilt</guid>
      <link>http://www.caring.com/blogs/caregiver-guilt/comments</link>
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      <title>Comment on Prolonged Grief, a New Psychological Disorder?</title>
      <description>April died 3/21/95....i'm her mom....i'm still trying to stay alive....prolongued grief is real</description>
      <author>Della</author>
      <pubDate>Fri, 14 Aug 2009 23:33:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/prolonged-grief</guid>
      <link>http://www.caring.com/blogs/prolonged-grief/comments</link>
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      <title>Comment on Prolonged Grief, a New Psychological Disorder?</title>
      <description>Since the death of my brother, 1989, then my sister, 1990, 8 months apart. I have not been able to pull my self back to the real me. This is when everything started in a downward spiral. I still see the fear in my brothers eyes when I told him I needed to be at work the next day and would be back that night. The nurses, assured me he was going to pull through the stroke. The very next morning as I arrived at work. I recieved a phone call telling me my brother was brain dead. I later found out that his wife of 33 yrs. refused medical treatment upon arrival at the hospital, while he was still unconcious. Also, she insisted that the nurses needed me to sign a form stating he was brain dead. Later when my sister was dying, I asked her doctor if a brain dead person shed tears when you talked to them. I was ask to do this on the night he died by his wife. I ask her why, they said he was brain dead. She could not or would not answer that question. As I talked to him of my love for him and to for him to tell our mother in heaven hi for me. There were tears running down his face. My sister's doctor informed me he was not brain dead. I was told at the funeral for his wife in 2003, but the grown children they would buy headstones. He had already been dead several years. They were not buried next to each other she was placed some distance away with her mother. 2007, I went to a funeral at the cemetary expecting to find his grave, still no headstone, 19 yrs. after his death. I purchased one and had it put up on his birthdate a few months later. The fear in his eyes still haunt me and I still cry and can not talk about him. He was my brother, best friend and acting father, our own father did not care about us. I was 6 when mom died and he was 12.  I was lied to by the wife, hospital and ask to sign his death warrant. To this day it is still extremely painful.</description>
      <author>Anna1945</author>
      <pubDate>Thu, 13 Aug 2009 21:23:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/prolonged-grief</guid>
      <link>http://www.caring.com/blogs/prolonged-grief/comments</link>
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      <title>Comment on A &quot;Perfect Mom,&quot; a Bottle of Vodka, and 8 Dead: Why We Must Learn to Recognize Alcoholism in Women</title>
      <description>I am a daughter of a father alcoholic but I read this post with great interest and sadness. I can really see how, insidiously, women alcoholics *could* be more likely to hurt others. Very sad. Thank you for being unafraid to confront this.</description>
      <author>Anonymous</author>
      <pubDate>Thu, 13 Aug 2009 05:30:28 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alcoholism-in-women</guid>
      <link>http://www.caring.com/blogs/alcoholism-in-women/comments</link>
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      <title>Comment on A &quot;Perfect Mom,&quot; a Bottle of Vodka, and 8 Dead: Why We Must Learn to Recognize Alcoholism in Women</title>
      <description>this is an excellent post.  I am a recovering alcoholic, my mother is an alcoholic.  Anyone who thinks their mother, sister, friend may have a drinking problem should read this post.  </description>
      <author>marfagirl</author>
      <pubDate>Thu, 13 Aug 2009 00:03:26 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alcoholism-in-women</guid>
      <link>http://www.caring.com/blogs/alcoholism-in-women/comments</link>
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      <title>Comment on A &quot;Perfect Mom,&quot; a Bottle of Vodka, and 8 Dead: Why We Must Learn to Recognize Alcoholism in Women</title>
      <description>Powerful blog. I appreciated reading this.</description>
      <author>Anonymous</author>
      <pubDate>Wed, 12 Aug 2009 15:12:33 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alcoholism-in-women</guid>
      <link>http://www.caring.com/blogs/alcoholism-in-women/comments</link>
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      <title>Comment on Surprising New Research: Is It Alzheimer's--or a Vision Problem?</title>
      <description>While your comment about covering mirrors to reduce glare is a good idea..we found that by putting mirrors on the inside of doors we did not want patients to leave through..was a great deterent to them attempting to get out through those doors.  We think it was because of their inability to always recognize themselves and they just thought there was a person blocking the exit. </description>
      <author>GrannyB</author>
      <pubDate>Tue, 11 Aug 2009 22:41:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/improving-vision-for-alzheimers</guid>
      <link>http://www.caring.com/blogs/improving-vision-for-alzheimers/comments</link>
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      <title>Comment on How to Cope With Cancer Fear</title>
      <description>My prayers are with the person who posted the first comment.  Sometimes we do everything we are supposed to do, and we still don't find health issues in the earliest stages.  Cancer is never &quot;fair&quot; and is has affected too many of my own friends and relatives. One of my healthiest friends has stage IV lymphoma (going on 7 years). I have two friends who were diagnosed with stage IV colon cancer, 9 and 8 years ago respectively.  Both are still alive.  And a friend who was diagnosed with ovarian cancer in 1993--still alive and going strong.  </description>
      <author>Anonymous</author>
      <pubDate>Tue, 11 Aug 2009 19:39:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/cancer-fear</guid>
      <link>http://www.caring.com/blogs/cancer-fear/comments</link>
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      <title>Comment on How to Hang Out With Someone Who Has Alzheimer's</title>
      <description>These are all good ideas.  I agree that you have to be sure the person is up for a large visit of people, but if folks arrive at the same time but can string in a few at time, it may be less overwhelming. Older people love children, but if they are alzheimers AND sick, older people can only take noise and disruption for so long. In visiting my elderly dementia/alzheimers family/friends, I have found that offering to brush their hair or help them put some lotion on their hands is usually readily agreed to. If you can take them for a walk, get them outside if you have a nice day or somewhere they can see outside. Identifying yourself and those with you are a must. Patience - well, be ready to repeat yourself and do so with a smile.  They may have a problem remembering facts or people, but they have not forgotten what it feels like to be considered &quot;old&quot;. My mother said that she notices the &quot;winks and nods&quot; of people when she repeats herself and it hurts her feelings. She knows she is not &quot;on top of her game&quot; anymore, but those little social things are still noticed! Remember that sometimes the problem is not the mental aspect - it may be more a hearing or vision issue!</description>
      <author>pollytnjc</author>
      <pubDate>Tue, 11 Aug 2009 15:13:11 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/family-with-alzheimers/comments</link>
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      <title>Comment on Surprising New Research: Is It Alzheimer's--or a Vision Problem?</title>
      <description>This is good info. I'd also like to add that a hearing loss can result in behavior that appears to be alzheimers related too.  My mother was responding inappropriately to comments from others - in getting her a GOOD hearing aide, this &quot;problem&quot; has improved markedly. In addition, I am not sure if this is true, but a friend of mine whose mother was alzheimers patient who &quot;ran away&quot; alot, was told by nursing home attendents that putting a dark/black mat under the door would appear to be a hole to many alzheimers patients and would stop them from going out the door. Unfortunately, the aides did not tell her this until her mother had already passed away. She said if it would work, it would have saved her a lot of grief!  Anyone know about this?</description>
      <author>pollytnjc</author>
      <pubDate>Tue, 11 Aug 2009 15:03:17 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/improving-vision-for-alzheimers</guid>
      <link>http://www.caring.com/blogs/improving-vision-for-alzheimers/comments</link>
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      <title>Comment on Surprising New Research: Is It Alzheimer's--or a Vision Problem?</title>
      <description>Great article.

One more note on the dark throw rugs.  Depending on where a man grew up, a dark spot could be a hole to urinate in - if he grew up in the country.</description>
      <author>CA-Claire</author>
      <pubDate>Tue, 11 Aug 2009 14:41:28 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/improving-vision-for-alzheimers</guid>
      <link>http://www.caring.com/blogs/improving-vision-for-alzheimers/comments</link>
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      <title>Comment on What To Do When a Family Disagreement Makes Caregiving Way Harder Than It Needs To Be</title>
      <description>journey: you are doing the right thing. Sometimes our spouses are not as able to deal with their emotions very well when it involves people they care about. I witnessed my husband doing the same thing. It was easier for him to vent on me than admit what he was really feeling. My suggestion: be like teflon when this happens, don't let it stick to you. It's not about you, you are just in the line of fire.</description>
      <author>jpirron1</author>
      <pubDate>Mon, 10 Aug 2009 12:48:48 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be</guid>
      <link>http://www.caring.com/blogs/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be/comments</link>
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      <title>Comment on The Secret Guilt of Caregivers</title>
      <description>It's still hard to pass off the guilt. Also, guilt goes w/ depression sx's, too. Again, the more you delegate, or get help....the easier life is, &amp; guilt lessens.</description>
      <author>Spockula</author>
      <pubDate>Sun, 09 Aug 2009 06:17:31 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-guilt</guid>
      <link>http://www.caring.com/blogs/caregiver-guilt/comments</link>
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      <title>Comment on How to Cope With Cancer Fear</title>
      <description>I ama a female and just turned 60, and have always gone in for my annual physicals, or any other time I was not feeling well. Two years ago I got my first colonoscopy and was told no polps all was clear.  Last year I noticed my energy level droping and a feeling like there was something in my lower abdomen.  I thought it was my female organs having a problem.  I had no pain.  My doctor said I was a little anemic and could not feel or see anything with the exam.  Around February I started having pain in my lower right side. I thought it was my ovary.  I was still feeling tired a lot.  In March I went to the doctor again complaining of pain when I bent ove to put my shoes on.  I had a pelvic ultrasound and nothing howed up.  However, my blood test showed that I was iron deficient.  My doctor sent me for a CT scan, which showed I had a mass in my colon!  On June 1 I had a surgery to remove 12&quot; inches of my colon.  The mass was cancer, stage 3.  The only reason why I had pain was because the cancer started in my appendix then went through to the colon.  The doctor took 24 of my lymph nodes out and 4 were positive for cancer.  My margins were clear.  The surgeon said they got all the cancer, but I would need six months of chemotherapy as a preventative measure.  When I say the oncologist he ordered a PET scan, which unfortunately for me, showed 3 cancer spots on my liver, one just outside my liver and some small spots near my stomach which they were not sure of.  So now I am on a chemotherapy schedule, just finished my second session.  So even though I did was I was supposd to do, annual exams, my colonoscopy, somehow this cancer was missed.  How upsetting this has been for me and my family.  Two years ago if the doctor had found it during the colonoscopy, maybe it would have been a stage 1 or 2 and not spread to my other organs.  My prognosis?  I don't know.  I will be starting a 3rd medication with my 3rd chemo session.  The medication is Avstin, which I hear is a very good life saving drug.</description>
      <author></author>
      <pubDate>Sun, 09 Aug 2009 04:44:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/cancer-fear</guid>
      <link>http://www.caring.com/blogs/cancer-fear/comments</link>
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      <title>Comment on The Secret Guilt of Caregivers</title>
      <description>I thought this was very helpful...My sister and I are now dealing with this guilt.  My mom lives with my sister (who works day, nights and weekends) and I take care of Mom when my sister cannot be there.  I also do all doctor, hairdresser, eye doctor appointments, etc.  If Mom wants to go out, I take her.  But we recently had a weekend where both my sister and I wanted to have a break and you should have heard Mom.  You girls don't love me anymore because you don't want me around....I'm telling you it was difficult!!! So thanks for the comments... Keep them coming</description>
      <author>PT Cruzr</author>
      <pubDate>Sat, 08 Aug 2009 17:41:29 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-guilt</guid>
      <link>http://www.caring.com/blogs/caregiver-guilt/comments</link>
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      <title>Comment on The Secret Guilt of Caregivers</title>
      <description>Very good article.  Helps me understand my guilt better.  Guilt isn't going away, I can just look at it differently and then compartmentalize it.</description>
      <author>CA-Claire</author>
      <pubDate>Fri, 07 Aug 2009 14:58:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-guilt</guid>
      <link>http://www.caring.com/blogs/caregiver-guilt/comments</link>
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      <title>Comment on The Secret Guilt of Caregivers</title>
      <description>Very good article.  Helps me understand my guilt better.  Guilt isn't going away, I can just look at it differently and then compartmentalize it.</description>
      <author>CA-Claire</author>
      <pubDate>Fri, 07 Aug 2009 14:58:31 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-guilt</guid>
      <link>http://www.caring.com/blogs/caregiver-guilt/comments</link>
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      <title>Comment on The Secret Guilt of Caregivers</title>
      <description>Very good article.  Helps me understand my guilt better.  Guilt isn't going away, I can just look at it differently and then compartmentalize it.</description>
      <author>CA-Claire</author>
      <pubDate>Fri, 07 Aug 2009 14:58:28 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-guilt</guid>
      <link>http://www.caring.com/blogs/caregiver-guilt/comments</link>
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      <title>Comment on The Secret Guilt of Caregivers</title>
      <description>Very good article.  Helps me understand my guilt better.  Guilt isn't going away, I can just look at it differently and then compartmentalize it.</description>
      <author>CA-Claire</author>
      <pubDate>Fri, 07 Aug 2009 14:58:16 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-guilt</guid>
      <link>http://www.caring.com/blogs/caregiver-guilt/comments</link>
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      <title>Comment on The Secret Guilt of Caregivers</title>
      <description>Very good article.  Helps me understand my guilt better.  Guilt isn't going away, I can just look at it differently and then compartmentalize it.</description>
      <author>CA-Claire</author>
      <pubDate>Fri, 07 Aug 2009 14:58:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregiver-guilt</guid>
      <link>http://www.caring.com/blogs/caregiver-guilt/comments</link>
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      <title>Comment on What To Do When a Family Disagreement Makes Caregiving Way Harder Than It Needs To Be</title>
      <description>Oh God!! I was going to write about this very subject just yesterday, but, my mother-in-law (who has middle stage dementia/Alzheimer's) fell and I was wrapped up in taking care of her. 
I am the sole caregiver of my mother-in-law. I see to her every need, including talking with all the doctors and dealing with the pallative care group that comes into the home. Its from my observations that they come up with a medicine plan for her. She is progressing rapidly with the disease right now and we have had to add a couple of new medicines. I try to explain to my husband (her son - who does literally nothing to help me..even though he works at home) the need for the medicines and what to expect from them, especially the first few days while her body is adjusting to them. He throws a fit and blames the rapid progression of her disease on the medicines. I print off articles from the internet that describes the disease and its stages, yet, he doesn't seem to get it. Its so frustrating to me. He goes on and on about it so much that I start to second guess myself and the doctors/nurses that are taking care of her over the medicines. He makes me feel guilty that I could be adding to her condition and making her worse. We tried to set up a family meeting with the doctors, nurses and case worker assigned to her from the pallative care group so that he would finally get it, but, so far, haven't been able to do it. After her fall yesterday, I told my husband about it and, of course, he blamed it all on the medicines, although he knows she's been falling for years, long before any hardcore medicines were introduced to her. I called her nurse and had her come out, just to make sure my mother-in-law was okay. I explained (again) to the nurse my husband's reaction. After she left (mother-in-law was shaken but fine, btw), she called my mother-in-law's primary care doctor and explained to him what was going on. They called me this morning to set up an appointment with my mother-in-law, my husband and myself. I'm not sure how he's going to take this and am worried about it. My main goal is to make whatever time my mother-in-law has left as pain free and peaceful as I can. I would never allow anything to happen to her that would hurt her, but, am so close to telling the husband to find someone else to take care of her, yet, I know that no one else will. They will say, &quot;put her in a home&quot;, and I don't want to do that as long as I can. 
Obviously, a mediator won't work in my situation. Does anyone have any suggestions for me on how to deal with a spouse that is battling me on everything, yet, really has no clue as to what is going on??
Sorry I went on and on...just really need some advice here. Thanks!</description>
      <author>Journey002</author>
      <pubDate>Thu, 06 Aug 2009 15:27:29 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be</guid>
      <link>http://www.caring.com/blogs/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>The relationship between my sibling and I is so
broken, due to lack of support all around, and distancing
away from my concerned calls very early during moms changes.

I have been A caregiver for my mom now going on 6 years now. So happens I am the youngest,so have lived with mom longer, infact never left her side, She an aging widow me commited to make it as the first college grad in the family. My mother became very supportive of my wishes to further my education. So we settled in a small nice community senior friendly and single professional types; I convinced mom it was ideal for both, while I now worked on a solid 10 year career path, she can relax and socialize in the community. Alot seem to happen before mother demntia surfaced; Her oldes son passes away suddenly in 2001 from cardiac arrest, she had no greiving support from anyone, calls just stopped.
Delusional dreams, awoke her in sweat, claiming to
have overheard my brother say, &quot;mom I bleed&quot;,
then another of an Angel saying do not go back to sleep,
they will be comming for you soon, Then it worsend to a point, where her fear was for me. After several incidences of her walking out to find me at a hospital;
We finally got my mother then 66 of age into an evaluation center for two weeks. It was found to be Dementia of the Alzheimers type with early delusion.
My college minor in Psychology awakened my concerns early; so I had always engaged her in long talks about movies we'd watch; and so now that I look back I had always been trying to keep her relaxed and calm.
 According to the Doctors
We caught the illness early. mom's treatment began with Namenda,Zoloft and Lipitor
I still do not understand how I could not have seen
how radically she loss weight, She had began entering my room in sweat over hearing my brother speak to her over her bed, then i assumed because of the War in Iraq; she ran out saying she heard voices of things happening to other relative aswell. The economy then forced me to work double cause the Economy was realy bad then.
Homecare was obtained and a side from her grumpy demenor with the aides and her resistance to her
privacy being invaded and others doing hercooking, Her condition improved voices were gone due to louder tv watching.and talkative homeaides. 
Gradually over the years I took over things she could no longer do for herself billing,banking, food shopping,medication management, and many others.
My hope was to keep who she was intact; contagiouse laugher and loving person., We never mentioned the A word
in her precence.
Doctor's said it was Dementia of the AD type with early hallucinations and Depression features. Unfotunaly three years after a home attendant accompaning my mom to a med appointment loss mom on a bus, mom got off and was loss 20 hours. found exhausted the following morning at a local hospital 100 block away from where they boarded the bus.
My (now feuding sibling) other sibling became erradic and decided to practically take her from me; an absentee, uninvolved, arguementative so long away from her care. Became a very ugly situation,.
When the smoke cleared and mom back home with me; 
I changes that were not there before, I noticed mom conversing with stuffed animals as if they were children, and unable to go the the bath room so near her bedroom; and would go anywhere. 
I could not understand if the 20 hours with out her medication caused her to further lose her mental stability? or if others may have given her unprescribed meds since &quot;jane doe&quot; had no ID.? I still have no clue; but the recentment fell at that point, I followed her closley and recognized cognitive decline, but not these symptoms they seemed different somehow? In 2007 moms 10 year old application for rental susidy asst
came through and was able to relocated to a neighboring state borderline but close to transportation. The move was needed due to her changes and so we moved from a studio 1br to a two bedroom railroad apt; She is visible to me from all rooms which is perfect now that I can care for her fulltime.

Very unusual to me now, is the sudden changes that happened to mom almost the next day. Mom could not stay still..... literally,....., Its so not like her......... to not watch her favorite channels peacfully. when I tell you
Severe restlessness &quot;I mean&quot;
all day pacingup and down; no medications were missed or changed. So I don't understand why this is possible, Symptoms as they progress are common but so are medication withrawl symptoms. Is it that mom is so 
overwhelmingly happy? I do not know., But very concern Now I find my self running after her all the time? Can anyone share if this is in fact Akathisia is normal or if it is typical to begin overnight? or if someone may have used something not consulted with doctors, while I worked?
Neighbors here feel it is wonderfull excercise; But she also started whimpering expressions or cry urge around the same time. If any of you ever knew my mother she has been known for her (Loretta Switt m.a.s.h) strength to my family,.. a true srgnt.
I am very restless, over her restlessness any infomation or advise for mom and moms last son and moms only daughter? Advice welcomed********************** right away; from &quot;Whatagoodson&quot;
********************** Thankyou. roberto</description>
      <author>Whatagoodson</author>
      <pubDate>Thu, 06 Aug 2009 07:01:13 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on Bad News for Menopausal Women: Hormone Therapy Boosts Ovarian and Breast Cancer Risk</title>
      <description>I am always impressed by the information from the Women-to_women Clinic.  Here's an article about this... 
http://www.womentowomen.com/bioidentical-hrt/perspectiveonrisks.aspx
</description>
      <author>Rebecca</author>
      <pubDate>Wed, 05 Aug 2009 21:43:57 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/hormone-replacement-therapy-risk</guid>
      <link>http://www.caring.com/blogs/hormone-replacement-therapy-risk/comments</link>
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      <title>Comment on Bad News for Menopausal Women: Hormone Therapy Boosts Ovarian and Breast Cancer Risk</title>
      <description>This is a really good question. I will need to look into it, as the issues related to taking hormones post-hysterectomy are different. I'll cover this in a future post!</description>
      <author>Melanie Haiken</author>
      <pubDate>Wed, 05 Aug 2009 19:46:20 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/hormone-replacement-therapy-risk</guid>
      <link>http://www.caring.com/blogs/hormone-replacement-therapy-risk/comments</link>
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      <title>Comment on Bad News for Menopausal Women: Hormone Therapy Boosts Ovarian and Breast Cancer Risk</title>
      <description>I guess I need some clarification. First of all, if I am on estrogen only, and the reason I am on hormones is because I had my ovaries removed, is there still a risk? 
Secondly, as I read the article on breast cancer, it was referring to women who take estrogen with progestins. Therefore, if I take estrogen only, what is the increased risk of breast cancer?
This is all so confusing.  I had a total hysterectomy three weeks before the original study came out. I had done lots of homework on the available information at the time and met for two hours with a consulting nurse in order to make an informed decision. And then three weeks into my recovery all the information I had learned was discounted.
I have tried to go off the hormones, but in addition to debilitating hot flashes (every 20 minutes around the clock that not only make me sweat, but begin with an intense surge of nausea), I also get severe migraines, the kind that make me throw up and require that I lay motionless in a dark room for hours. Fun huh!
Right now the only thing that keeps me functioning is the estrogen! 
So, based on the fact that I have no ovaries and take estrogen only, what is the actual risk of ovarian and breast cancer in my situation?
</description>
      <author></author>
      <pubDate>Wed, 05 Aug 2009 13:13:14 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/hormone-replacement-therapy-risk</guid>
      <link>http://www.caring.com/blogs/hormone-replacement-therapy-risk/comments</link>
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      <title>Comment on How to Hang Out With Someone Who Has Alzheimer's</title>
      <description>Great thoughts! When my grandchildren are here, it is fun for my father with alzheimers to participate in whatever he can. Twice, at birthdays, balloons have been part of our day for our 3-6 yr. old grandchildren. We ALL had a great time batting them from one person to the next and great grandpa never got tired of it, much to the kids' deight!</description>
      <author>maryl</author>
      <pubDate>Tue, 04 Aug 2009 22:05:13 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/family-with-alzheimers/comments</link>
    </item>
    <item>
      <title>Comment on How to Hang Out With Someone Who Has Alzheimer's</title>
      <description>I agree with most of what you say, but before any of that, be sure your &quot;person&quot; is up to a large group of people, especially kids.  I've had that blow up in my face...usually better to limit it to 2or 3 at the most at a time.  Watch for signs of agitation and end it quickly if you see a problem.</description>
      <author></author>
      <pubDate>Tue, 04 Aug 2009 17:29:49 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/family-with-alzheimers/comments</link>
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      <title>Comment on Health Alert: 7 Vaccines Few Adults Have Had -- But Need</title>
      <description>You don't mention that 40% of vaccines today come from China, a country with a terrible inspection record.  It has the highest rejection rate of imports and its factory inspection rate shows that it cannot be depended on to follow safety requirements.  (*The FDA only checks these vaccine factories once every 13 years!!).  Also, sadly,  many deaths from flu and pneumonia are caused by hospital errors/weakness from bad nutrition. *The info on vaccines came from Dr. Russell Blaylock. 
</description>
      <author>jorie13</author>
      <pubDate>Tue, 04 Aug 2009 16:42:22 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/adult-vaccination</guid>
      <link>http://www.caring.com/blogs/adult-vaccination/comments</link>
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      <title>Comment on How to Hang Out With Someone Who Has Alzheimer's</title>
      <description>It's all helpful, I am just starting out with caring for my Pops finding out were he is at mentally and physically has been and eye opener to say the least. He has been living in another city and a couple of my siblings have been taking advantage of him from a money stand point so now he has no money other than him SS. I am the only child who is in a position with time to some what care for him along with my very understanding wife. It's great to have a spot on the internet which is this helpful. My wife and I have taken Pops onto our property in a fifth wheel trailer which is very nice for him he seems to be happy here. But doesn't seem to understand this is now the place where he will live from now on. We are going to his home in another town which he has moved from and pack more of his belongings letting him say what goes and what doesn't. Hoping this will help put some input to the move. we are also putting together a visual calender for him with a daily schedule. We are having some difficulty keeping him active he is 79 years young so activity I am hoping will help him have a more complete life and help him mentally also. For the most part he understands 50% of what is happening in his life right now lots of changes currently so he gets lost in it a bit. Anyway I just wanted to say not alone hoping the journey will be and enjoyable one.   </description>
      <author>robert k</author>
      <pubDate>Tue, 04 Aug 2009 15:52:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/family-with-alzheimers/comments</link>
    </item>
    <item>
      <title>Comment on How to Hang Out With Someone Who Has Alzheimer's</title>
      <description>It's all helpful, I am just starting out with caring for my Pops finding out were he is at mentally and physically has been and eye opener to say the least. He has been living in another city and a couple of my siblings have been taking advantage of him from a money stand point so now he has no money other than him SS. I am the only child who is in a position with time to some what care for him along with my very understanding wife. It's great to have a spot on the internet which is this helpful. My wife and I have taken Pops onto our property in a fifth wheel trailer which is very nice for him he seems to be happy here. But doesn't seem to understand this is now the place where he will live from now on. We are going to his home in another town which he has moved from and pack more of his belongings letting him say what goes and what doesn't. Hoping this will help put some input to the move. we are also putting together a visual calender for him with a daily schedule. We are having some difficulty keeping him active he is 79 years young so activity I am hoping will help him have a more complete life and help him mentally also. For the most part he understands 50% of what is happening in his life right now lots of changes currently so he gets lost in it a bit. Anyway I just wanted to say not alone hoping the journey will be and enjoyable one.   </description>
      <author>robert k</author>
      <pubDate>Tue, 04 Aug 2009 15:52:06 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/family-with-alzheimers/comments</link>
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      <title>Comment on How to Hang Out With Someone Who Has Alzheimer's</title>
      <description>What great ideas!  I will keep them in mind for my parents, although there are only 2 grandchildren which are over 18 now.
Sometimes it's difficult to have conversations with my parents, whom I believe are in the early stages of dementia - Mom has 4 of the 8 symptoms, and Dad has the other 4, which is how they were able to hide it for so long.
We are too late on the photo albums, they are unable to remember the photos that are unlabelled.  Wish I had taken an interest earlier.
The repetition is difficult, but we try to cope with it. 
Thank you so much for sharing!</description>
      <author>CA-Claire</author>
      <pubDate>Tue, 04 Aug 2009 14:57:25 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/family-with-alzheimers/comments</link>
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      <title>Comment on How to Hang Out With Someone Who Has Alzheimer's</title>
      <description>My grandchildren visit my husband frequently.  To make it more comfortable for them, we plan to entertain him.  Once a granddaughter did her tap dance routine, the grandson demonstrated Tai Kwan Do and talked aboiut his black belt.  Another time all of the grandkids came and decorated their Easter eggs in the activity room.  Lots of pictures and laughing.  We &quot;invented&quot; a 500 mile race.  We bought 4 tiny pull back cars in different colors.  We made a simple track of plastic framing material and taped it to the table so the cars couldn't fall off.  We had a stop ramp of the same at the end. Lots of flag decorations.  All took their turn while the rest guessed which car would win.  We can even play it again!  Bob enjoyed it all and the grandkids felt needed.</description>
      <author>Joy Golliver</author>
      <pubDate>Tue, 04 Aug 2009 14:36:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/family-with-alzheimers/comments</link>
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      <title>Comment on How to Hang Out With Someone Who Has Alzheimer's</title>
      <description>much appreciated</description>
      <author>batarina</author>
      <pubDate>Tue, 04 Aug 2009 14:13:36 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/family-with-alzheimers/comments</link>
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      <title>Comment on How to Hang Out With Someone Who Has Alzheimer's</title>
      <description>Thanks...very helpful.  Liked the cookie idea!!</description>
      <author></author>
      <pubDate>Tue, 04 Aug 2009 14:03:00 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/family-with-alzheimers</guid>
      <link>http://www.caring.com/blogs/family-with-alzheimers/comments</link>
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      <title>Comment on Safe Sleep Tips to Prevent Stroke</title>
      <description>I HAVE SLEEP APNEA AND IT'S TERRIBLE.  I AM CONSTANTLY TIRED AND RARELY HAVE ENERGY TO PERFORM EVEN THE MOST SIMPLE DAILY TASKS.  I HAVE STARTED USING A C-PAP MACHINE AND IT SEEMS TO HELP,ALTHOUGH I HAVEN'T BEEN USING IT VERY LONG.  I WAS TOLD THAT AFTER A FEW MONTHS OF USING IT,I WILL BE ABLE TO TELL A TOTAL DIFFERENCE.  I CAN HARDLY WAIT.  SLEEP APNEA CAN CAUSE SO MANY PROBLEMS, LIKE DEPRESSION,FORGETFULNESS,ANXIETY AND IRRITABILITY TO NAME A FEW.  I WAS TOLD THAT I WAS LUCKY THAT I DIDN'T DIE IN MY SLEEP,ALREADY!!  THIS IS VERY SERIOUS AND NOTHING TO PLAY WITH.  IF YOU THINK YOU MAY HAVE SLEEP APNEA OR HAVE ANY OF THE PROBLEMS LISTED, YOU SHOULD AT LEAST BE TESTED.  IT CAN'T HURT AND YOU HAVE NOTHING TO LOSE,BUT SLEEP!!  THAT'S ENOUGH!  I'M SO GLAD THAT I WAS TESTED.  I HOPE ANYONE WHO EVEN THINKS THEY HAVE IT WILL BE TESTED A.S.A.P.  GOOD LUCK AND GOD BLESS YOU!    MCKI777</description>
      <author>Mcki777</author>
      <pubDate>Tue, 04 Aug 2009 04:44:53 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sleep-apnea-can-cause-strokes-safety-tips</guid>
      <link>http://www.caring.com/blogs/sleep-apnea-can-cause-strokes-safety-tips/comments</link>
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      <title>Comment on Sasha and Malia Obama's Parents Have Living Wills, How About Yours?</title>
      <description>It was quite an eye-opener. With age catching up, one does think about these situations.  But it never occurred that one can prepare a living will.  It should be mandatory. One can't leave these decisions to others.

Thanks a lot!</description>
      <author></author>
      <pubDate>Fri, 31 Jul 2009 00:53:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/obamas-living-wills</guid>
      <link>http://www.caring.com/blogs/obamas-living-wills/comments</link>
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      <title>Comment on What To Do When a Family Disagreement Makes Caregiving Way Harder Than It Needs To Be</title>
      <description>Though it is a good idea to have a mediator for resolving family disagreements for care giving, how do we know that the mediator is not biased by his mindset.  I know of cases where the woman is always held responsible for every problem that arises in the family, whether it be a heavy electricity bill, kids not faring well in school, the food not being palatable enough. In short even a superwoman would be a failure. How does one find a reliable mediator who does not add fuel to the fire?</description>
      <author></author>
      <pubDate>Fri, 31 Jul 2009 00:40:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be</guid>
      <link>http://www.caring.com/blogs/what-to-do-when-a-family-disagreement-makes-caregiving-way-harder-than-it-needs-to-be/comments</link>
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      <title>Comment on Which Painkillers Are Safe for Seniors?</title>
      <description>I did not mean the comment below to be anonymous. It was from the author, Melanie Haiken.</description>
      <author>Melanie Haiken</author>
      <pubDate>Thu, 30 Jul 2009 22:30:22 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/painkillers</guid>
      <link>http://www.caring.com/blogs/painkillers/comments</link>
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      <title>Comment on Which Painkillers Are Safe for Seniors?</title>
      <description>The panel said they primarily focused on those age 75 or older. However, I bought an NSAID myself yesterday and noticed that the new &quot;black box&quot; warning on the box applies to age 60 and up. This is a good question and I'll address it more in a future post.</description>
      <author>Anonymous</author>
      <pubDate>Thu, 30 Jul 2009 22:29:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/painkillers</guid>
      <link>http://www.caring.com/blogs/painkillers/comments</link>
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      <title>Comment on Which Painkillers Are Safe for Seniors?</title>
      <description>How does the author or the Society define a &quot;senior&quot; and/or an &quot;older adult&quot;?  Also for those of us who belong to large HMOs, who like to use NSAIDs and are extremely hesitant to prescribe narcotics, what can a patient to do to help change the formulary policies?</description>
      <author>Tater</author>
      <pubDate>Thu, 30 Jul 2009 01:42:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/painkillers</guid>
      <link>http://www.caring.com/blogs/painkillers/comments</link>
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      <title>Comment on Is This Alzheimer's Prevention Advice Worth Changing Your Life Over?</title>
      <description>



Good advice</description>
      <author></author>
      <pubDate>Wed, 29 Jul 2009 01:30:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/alzheimers-studies</guid>
      <link>http://www.caring.com/blogs/alzheimers-studies/comments</link>
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      <title>Comment on Oral Histories: Preserving Your Family's Stories</title>
      <description>This is a great tip...one I used with my Mother before she died back in July 2000....Mom was in a nursing home and it was hard to visit because she complained about every pain she had.
I came up with the idea of &quot;Interviewing Mom&quot; and she LOVED it...I would take her a McDonald's Happy meal(she loved them) or a pizza and her Diet Pepsi and she was in heaven...She was important...she had my complete attention...she loved it. I was able to visit with her and I was rewarded with stories of her life that I would never had heard.</description>
      <author></author>
      <pubDate>Tue, 28 Jul 2009 16:11:52 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/oral-histories</guid>
      <link>http://www.caring.com/blogs/oral-histories/comments</link>
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      <title>Comment on Prostate Cancer Therapy May Do More Harm Than Good</title>
      <description>Re: prostate hormonal therapy (lupron): a decade back I dealt with prostate cancer. I survived by getting out from under a urologist at a local medical facility &amp; finding another out of town. I did try alternatives with minor success combined with orthodox therapy. Orthodox at the time being lupron and my urologist (at the time) a money hungry  doc had me coming one to two times a months for: 1- 2 office visits often charging a 'double' office visit, or a scan or imaging or his favorite form of torture prostate biopsy ( several times even though he already established I had prostate cancer).  I took lupron several months (about $1,000 /month lupron alone). Side effects were nasty. In my opinion lupron should be outlawed. One nasty side effect was fibromyalgia (although medical establishment disagrees). Finally found an answer for that on my own about 9 months later. But today, I have what may be residual problems with muscle tissue - that is constant pain, misery &amp; discomfort although, admittedly, i can't prove it. (Fibromyalgia comes in several different forms.) There were other miserable effects like taking on a new personality: anger, fits of hyperactivity, wanting to smash cars on the freeway (wonder how many have done that). It caused lot other nasty side effects but not one good came out of it.  By the way - I finally got out from under that doc and found a real doctor. Fortunately, all doctors are not alike and that applies to medical facilities as well. It pays to 'shop around'. And if you encounter a urologist surgeon that insists on blood transfusions - don't hesitate - leave promptly. That is old fashioned, no longer necessary. It does indicate that surgeon should be working in a meat shop, not operating on humans.

GF San Diego, CA</description>
      <author>gffoye</author>
      <pubDate>Tue, 28 Jul 2009 00:06:31 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/tprostate-cancer-therapy-may-do-more-harm-than-good</guid>
      <link>http://www.caring.com/blogs/tprostate-cancer-therapy-may-do-more-harm-than-good/comments</link>
    </item>
    <item>
      <title>Comment on Prostate Cancer Therapy May Do More Harm Than Good</title>
      <description>Re: prostate hormonal therapy (lupron): a decade back I dealt with prostate cancer. I survived by getting out from under a urologist at a local medical facility &amp; finding another out of town. I did try alternatives with minor success combined with orthodox therapy. Orthodox at the time being lupron and my urologist (at the time) a money hungry  doc had me coming one to two times a months for: 1- 2 office visits often charging a 'double' office visit, or a scan or imaging or his favorite form of torture prostate biopsy ( several times even though he already established I had prostate cancer).  I took lupron several months (about $1,000 /month lupron alone). Side effects were nasty. In my opinion lupron should be outlawed. One nasty side effect was fibromyalgia (although medical establishment disagrees). Finally found an answer for that on my own about 9 months later. But today, I have what may be residual problems with muscle tissue - that is constant pain, misery &amp; discomfort although, admittedly, i can't prove it. (Fibromyalgia comes in several different forms.) There were other miserable effects like taking on a new personality: anger, fits of hyperactivity, wanting to smash cars on the freeway (wonder how many have done that). It caused lot other nasty side effects but not one good came out of it.  By the way - I finally got out from under that doc and found a real doctor. Fortunately, all doctors are not alike and that applies to medical facilities as well. It pays to 'shop around'. And if you encounter a urologist surgeon that insists on blood transfusions - don't hesitate - leave promptly. That is old fashioned, no longer necessary. It does indicate that surgeon should be working in a meat shop, not operating on humans.

GF San Diego, CA</description>
      <author>gffoye</author>
      <pubDate>Tue, 28 Jul 2009 00:06:30 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/tprostate-cancer-therapy-may-do-more-harm-than-good</guid>
      <link>http://www.caring.com/blogs/tprostate-cancer-therapy-may-do-more-harm-than-good/comments</link>
    </item>
    <item>
      <title>Comment on Prostate Cancer Therapy May Do More Harm Than Good</title>
      <description>Re: prostate hormonal therapy (lupron): a decade back I dealt with prostate cancer. I survived by getting out from under a urologist at a local medical facility &amp; finding another out of town. I did try alternatives with minor success combined with orthodox therapy. Orthodox at the time being lupron and my urologist (at the time) a money hungry  doc had me coming one to two times a months for: 1- 2 office visits often charging a 'double' office visit, or a scan or imaging or his favorite form of torture prostate biopsy ( several times even though he already established I had prostate cancer).  I took lupron several months (about $1,000 /month lupron alone). Side effects were nasty. In my opinion lupron should be outlawed. One nasty side effect was fibromyalgia (although medical establishment disagrees). Finally found an answer for that on my own about 9 months later. But today, I have what may be residual problems with muscle tissue - that is constant pain, misery &amp; discomfort although, admittedly, i can't prove it. (Fibromyalgia comes in several different forms.) There were other miserable effects like taking on a new personality: anger, fits of hyperactivity, wanting to smash cars on the freeway (wonder how many have done that). It caused lot other nasty side effects but not one good came out of it.  By the way - I finally got out from under that doc and found a real doctor. Fortunately, all doctors are not alike and that applies to medical facilities as well. It pays to 'shop around'. And if you encounter a urologist surgeon that insists on blood transfusions - don't hesitate - leave promptly. That is old fashioned, no longer necessary. It does indicate that surgeon should be working in a meat shop, not operating on humans.

GF San Diego, CA</description>
      <author>gffoye</author>
      <pubDate>Tue, 28 Jul 2009 00:06:29 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/tprostate-cancer-therapy-may-do-more-harm-than-good</guid>
      <link>http://www.caring.com/blogs/tprostate-cancer-therapy-may-do-more-harm-than-good/comments</link>
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      <title>Comment on Stress and the Music Cure</title>
      <description>What I love about this post is that is points out something we often forget: caregivers have to prioritize taking care of themselves.  It's hard to do, but it's so important.  I learned this lesson almost accidentally when my mom was diagnosed with Alzheimer's.  I'm not her primary caregiver, but her diagnosis changed my life nonetheless.  (I wrote about it recently on my blog.  I'll included the link, if you'd like to check it out: http://starfishenvy.typepad.com/starfish-envy/2009/07/you-spin-me-right-round-baby-right-round.html</description>
      <author></author>
      <pubDate>Sat, 25 Jul 2009 19:36:04 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/music-cure</guid>
      <link>http://www.caring.com/blogs/music-cure/comments</link>
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      <title>Comment on Stress and the Music Cure</title>
      <description>Thanks, this has been working with me...Mom will  have nothing but TV sound, so far.  I'm still working on her, starting with music radio in the car as we make our rounds.  I know it will help, as soon as I get through.  For me, it saves my sanity!</description>
      <author>jjobse</author>
      <pubDate>Fri, 24 Jul 2009 21:21:55 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/music-cure</guid>
      <link>http://www.caring.com/blogs/music-cure/comments</link>
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      <title>Comment on Stress and the Music Cure</title>
      <description>I am a private music teacher and church musician for more than 25 years.  In addition, for the last 10 years, I have been conducting choruses of seniors at senior centers and in assisted living and senior communities.  All the groups perform reguarly within their facilities and frequently in schools, for town events.  Two groups have performed with the local community symphony orchestra.  One group even went overseas to perform with another community group.  

Many of my chorus members have reported that their doctors comment that they don't know what they are doing in chorus, but whatever it is, they seem to be far healthier than before the joined the group.  One reason, I think (I'm not a therapist), is because I teach them to breath correctly, which promotes relaxation.  Several singers with cancer, have reported that they only get out of bed for doctor appointments and for chorus.  Chorus is the &quot;fun&quot; activity in their life that helps them get thru the rest of their week. 

Before I started working with seniors, I was aware that musicians are asked to play slower, more calming music in fine dining restaurants and when playing in a bar musicians are asked to play upbeat music.  This is because we unconcously eat, drink and move to the tempo heard.  In other words, economics gets involved in that restaurants don't want patrons to get indigestion so they require slower musc while bars make more money when patrons drink more.

As I have aged, my own osteoarthritis has gotten progressively worse and now, when I conduct a 30 minute performance, my knees hurt for the following two days.  I told my orthopedic (I'm to have replacement surgery) that the best pain killer I've found is making music.  While I am conducting I feel NO pain!  (I'm planning to take my ipod to PT)!

Over the years, I have also noted that when I am in emotional pain, making music focuses my insides and a 20 minute &quot;treatment&quot; soothes me and gives me a better perspective on whatever was causing the pain.

All this to say, I don't fully understand it, but I sure can attest that it works!</description>
      <author>LindaK</author>
      <pubDate>Fri, 24 Jul 2009 17:55:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/music-cure</guid>
      <link>http://www.caring.com/blogs/music-cure/comments</link>
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      <title>Comment on Foods That Prevent Memory Loss</title>
      <description>Interestingly, the study subjects didn't go on the DASH diet; their own diets were simply analyzed and it turned out that the people whose way of eating most resembled DASH -- which is an eating approach that seems to sum up what most doctors are saying is simply healthful basic nutrition -- did the best. So while I'm not an MD, it's hard to imagine this way of eating (a better description than the word &quot;diet&quot;) being &quot;bad&quot; for most people. (Your own doctor could address any tweaks specifically tailored to your medical situation, but they'd likely be tweaks, not major departures.)</description>
      <author>Paula Spencer</author>
      <pubDate>Tue, 21 Jul 2009 22:42:51 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/foods-that-may-prevent-memory-loss</guid>
      <link>http://www.caring.com/blogs/foods-that-may-prevent-memory-loss/comments</link>
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      <title>Comment on Foods That Prevent Memory Loss</title>
      <description>I find this to be very interesting. Not only because with out really knowing it, I have eating foods pertaining to the DASH diet, but because of the effects it has on our bodies. Although it's not sodium-reduced, would staying on this diet be bad for me even though I have hypo-tension? </description>
      <author>lolo23</author>
      <pubDate>Mon, 20 Jul 2009 17:39:18 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/foods-that-may-prevent-memory-loss</guid>
      <link>http://www.caring.com/blogs/foods-that-may-prevent-memory-loss/comments</link>
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      <title>Comment on Who's Worse Off: People With Alzheimer's&#8230;or Their Caregivers?</title>
      <description>I am 61 full time worker taking care of my 89 yr old mother-live with her. I have been doing this for 10 years.  She is healthier than me now.  I am stressed and about to lose my job.  She has no worries.  I take care of everything.  I have no social life and talk to myself a lot.  Ask me, the caregiver suffers more.  My mother may have thinking problems but is not aware of problems at all.  She has me who does her laundry, cooking, shopping, take her to the doctor, get her cleaned up...I do everything for her.  Some days after work and then doing for her I'm so tired I can't sleep.  There is no one to take care of me and we are running out of money.  So now I worry more than her, she doesn't worry at all.  Everyone says take care of yourself.  Have you tried finding time to do that?  I understand the concept and wish I could but how?  Now I also worry if I lose my job we both will be in financial trouble.  The patient with dementia has no such worries, my mom doesn't think any more.</description>
      <author>LindaSD</author>
      <pubDate>Sat, 18 Jul 2009 19:02:17 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/whos-worse-off-people-with-alzheimers-or-their-caregivers</guid>
      <link>http://www.caring.com/blogs/whos-worse-off-people-with-alzheimers-or-their-caregivers/comments</link>
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      <title>Comment on Foods That Prevent Memory Loss</title>
      <description>The DASH Diet is wonderful.  But it is not sodium-reduced.  The original DASH Study confirmed an 11.4 mmHg SBP fall on the DASH Diet with sodium held constant (among hypertensives).  A second, DASH-Sodium, study found hypertensives on the DASH Diet with 60% salt reduction achieved an 11.5 mmHg SBP fall.  The &quot;DASH effect&quot; is what is observed; the &quot;sodium effect&quot; is statistical noise.

That is what Heidi Wengreen found as well.  Sodium was tested independently and contributed nothing to the benefit of the DASH Diet with regard to mental function in the elderly.

Dick Hanneman
President
Salt Institute</description>
      <author>rhanneman</author>
      <pubDate>Sat, 18 Jul 2009 02:05:58 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/foods-that-may-prevent-memory-loss</guid>
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      <title>Comment on Who's Worse Off: People With Alzheimer's&#8230;or Their Caregivers?</title>
      <description>A caregiver must take care of themselves or someone will be taking care of them. I find myself gradually saying good-bye to the spouse that I love dearly and try to remember each day all of the years that he worked so hard to take care of me and our big family. I'm not saying that it is not hard because it really is. But now I recognize the value of Day Care and the time I have to read, meditate, have a little recreation at times and just have some time for myself. Keeping in contact over the phone with old friends is helpful and also sharing the experiences of the day with other caregivers </description>
      <author>1care</author>
      <pubDate>Thu, 16 Jul 2009 20:46:06 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/whos-worse-off-people-with-alzheimers-or-their-caregivers</guid>
      <link>http://www.caring.com/blogs/whos-worse-off-people-with-alzheimers-or-their-caregivers/comments</link>
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      <title>Comment on Who's Worse Off: People With Alzheimer's&#8230;or Their Caregivers?</title>
      <description>I understand the point of the article, but I basically disagree - I constantly strive to remember it's not about ME, the caregiver - it is about my WIFE, who is lost. She may not remember it 5 minutes later, but she lives it 24 hours a day. In choosing whether to place her or not, I worry about what is best for HER more than what is best for ME. Maybe its because I have caregivers who provide a lot of help, but I hate the idea that I would place her because it was tough on me, if its not also better for her.</description>
      <author>kronhead</author>
      <pubDate>Wed, 15 Jul 2009 20:58:04 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/whos-worse-off-people-with-alzheimers-or-their-caregivers</guid>
      <link>http://www.caring.com/blogs/whos-worse-off-people-with-alzheimers-or-their-caregivers/comments</link>
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      <title>Comment on Who's Worse Off: People With Alzheimer's&#8230;or Their Caregivers?</title>
      <description>Yes, the dementia patient has their share of problems, but the Caregivers are worse off. The dementia patient may be agitated one minute, but 5 minutes later has forgotten if and what he/she has been agitated about. The Caregiver, on the other hand remembers everything and loses sleep and develops health problems trying to handle and solve all the problems and responsibilities involved with caregiving.</description>
      <author>doforanimals</author>
      <pubDate>Wed, 15 Jul 2009 20:05:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/whos-worse-off-people-with-alzheimers-or-their-caregivers</guid>
      <link>http://www.caring.com/blogs/whos-worse-off-people-with-alzheimers-or-their-caregivers/comments</link>
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      <title>Comment on Diabetes: Can't Get No Respect -- And Why It Should</title>
      <description>I am seeing a man with type 2 diabetes, and although I have one sister and one brother with it, he really doesn't talk much about what he needs to do for his diabetes.  I am working on improving his diet, and exercise, but find I meet with resistance from him.  I also know he totally blows his diet during the week when we are not together, eating a lot of prepared, highly processed foods, and not much fresh.  I need all the help I can get!  So, thanks!</description>
      <author>sisterspitfire</author>
      <pubDate>Wed, 15 Jul 2009 13:33:58 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/diabetes-cantt-get-no-respect-and-why-it-should</guid>
      <link>http://www.caring.com/blogs/diabetes-cantt-get-no-respect-and-why-it-should/comments</link>
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      <title>Comment on Who's Worse Off: People With Alzheimer's&#8230;or Their Caregivers?</title>
      <description>CAREGIVERS (Family Caregivers) - HANDS DOWN!</description>
      <author>GALOWA</author>
      <pubDate>Wed, 15 Jul 2009 01:05:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/whos-worse-off-people-with-alzheimers-or-their-caregivers</guid>
      <link>http://www.caring.com/blogs/whos-worse-off-people-with-alzheimers-or-their-caregivers/comments</link>
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      <title>Comment on Who's Worse Off: People With Alzheimer's&#8230;or Their Caregivers?</title>
      <description>My problem isn't the cost of care - Medicare and our state program help cover the major expenses.  My problem is this: How do you know/recognize when the time has come to put the patient into full-time care?  I agree that I need to care for Mom as long as I can; no one else will care for her or about her as I do, including family members who can't be bothered to even call her occasionally.  Homes are impersonal and cold no matter how well-run they are. I also know she is going to hate me for it.  But I also recognize that I can't do this forever.  It's a very stressful life for all of us.   </description>
      <author></author>
      <pubDate>Tue, 14 Jul 2009 18:42:19 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/whos-worse-off-people-with-alzheimers-or-their-caregivers</guid>
      <link>http://www.caring.com/blogs/whos-worse-off-people-with-alzheimers-or-their-caregivers/comments</link>
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      <title>Comment on Who's Worse Off: People With Alzheimer's&#8230;or Their Caregivers?</title>
      <description>Everyone's situation is different...   In my case, my mom was diagnosed at age 64 and is 65 now.  I have three young children.  My mom is divorced and lives alone.  The &quot;roadblocks&quot; mentioned in the article do any apply to me.  I would be happy to get my mom to day care or have someone else give a hand...fact is she DOES NOT have a rainy day fund nor do we...  This is her rainy day and we are still trying to find an umbrella!!  My mom's quite content living in her middle stage world right now...she does not realize that her judgment is severly impaired and her memory is rapidly declining nor does she have empathy for the stress she has put on our family by choosing to spend her &quot;rainy day&quot; fund before she needed elder care.  Meanwhile, I see the rapid decline far too well and have not yet found the means with which to get her into some kind of assisted living.  From where I am right now...she is doing okay and I am on a steady decline both mentally and physically from the stress which this disease causes.  She has medications helping her cope...I do not...  I know my mom and I know myself and right now she is much better off than me...</description>
      <author>Cndy</author>
      <pubDate>Tue, 14 Jul 2009 16:52:10 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/whos-worse-off-people-with-alzheimers-or-their-caregivers</guid>
      <link>http://www.caring.com/blogs/whos-worse-off-people-with-alzheimers-or-their-caregivers/comments</link>
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      <title>Comment on Who's Worse Off: People With Alzheimer's&#8230;or Their Caregivers?</title>
      <description>I wonder how the person in the middle to later stages of Alzheimer's disease would respond.  No doubt those of us who are caregivers feel/live the stress of caring for a family member with Alzheimer's disease.  Protecting them, answering the same question a thousand times, cajoling them into bathing, and grieving for the relationship to go on as before, without change or interuption.  Meanwhile is it better to live with the stress and grief OR to be the care receiver filled with fear, surrounded by strangers, unable to protect oneself or flee from danger, and perhaps isolated (mentally, socially and spiritually). All suffer . . . neither one more than the other . . . just differently.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 14 Jul 2009 16:32:58 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/whos-worse-off-people-with-alzheimers-or-their-caregivers</guid>
      <link>http://www.caring.com/blogs/whos-worse-off-people-with-alzheimers-or-their-caregivers/comments</link>
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      <title>Comment on Who's Worse Off: People With Alzheimer's&#8230;or Their Caregivers?</title>
      <description>The Caregiver suffers the most. They know what is really going on. You can explain the the victim of the disease but they won't remember. You as the caregiver have to &quot;humor&quot; them. Not lying, but dancing around the questions ex: Where is my money? or I want to go home. or when they cry and can't recall the words their brain is trying to say. Being appreciated by the victim is not relevant in this.  The truth of the matter is no one will care for your loved one like you would..just as when your children were small, no one loves and raises your children as you do or good enough. At some point, you had to trust someone with your child, just as you have to trust someone with your loved one with Alzheimer's. AND remember things happen and it is usually no particular person's fault. </description>
      <author>Anonymous</author>
      <pubDate>Tue, 14 Jul 2009 13:20:51 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/whos-worse-off-people-with-alzheimers-or-their-caregivers</guid>
      <link>http://www.caring.com/blogs/whos-worse-off-people-with-alzheimers-or-their-caregivers/comments</link>
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      <title>Comment on Life's 5 Most Important Lessons </title>
      <description>laughter is the very best medicine... not original but true!</description>
      <author>Anonymous</author>
      <pubDate>Sun, 12 Jul 2009 20:01:24 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/notice-memory-loss-dont-forget-to-do-this</guid>
      <link>http://www.caring.com/blogs/notice-memory-loss-dont-forget-to-do-this/comments</link>
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      <title>Comment on 10 Early Signs of Prostate Cancer That Often Go Unnoticed</title>
      <description>my best friend and husband of 36 years goes to the VA hospital friday july17 for biopsey of the postate and he is terrified, because his brother is just now getting over the kemo, etc. for his cancer of the postate. any thing i can get to help me deal with this is so very helpful.  out youngest son 28years old just went in a mental ward for sucide attempt the second time since mothers day and my aunt (mama for 55years since the death of my mother at birth) has started kemo for cancer in the limpnods of her back.  out family is smothered in sickness of one time or other. thank you marm</description>
      <author>marm</author>
      <pubDate>Sun, 12 Jul 2009 15:11:20 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/signs-of-prostate-cancer</guid>
      <link>http://www.caring.com/blogs/signs-of-prostate-cancer/comments</link>
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      <title>Comment on Why Hospitals and Alzheimer's Are a Tough Mix</title>
      <description>I've had both my parents in the hospital this past year. Dad has Alzheimer's and Mom with dementia.  I have learned that the doctors, usually internists,  are concerned about the main complaint and don't continue the dementia meds.  Dad sundowned and Mom had hallucinations.  Now I stay the whole ER visit and talk to the floor nurse insisting on the demntia meds be given, even if she has to call the doctor again.  Unfortuneitly I learned the hard way.  Maybe this will help someone else.</description>
      <author>kam0614</author>
      <pubDate>Sat, 11 Jul 2009 19:21:03 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/why-hospitals-and-alzheimers-are-a-tough-mix</guid>
      <link>http://www.caring.com/blogs/why-hospitals-and-alzheimers-are-a-tough-mix/comments</link>
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      <title>Comment on How to Prevent Family Money Conflicts by Reconciling Money Styles</title>
      <description>I see some of the styles you describe in various people, but most people don't seem to exclusively fall into one category or another. Rather they tend to have characteristics of 2 or 3 with one being dominant. For example, my mother was probably a hoarder until she was about 50 or so. By that time her family was nearly raised and they were quite comfortable. She had always had a bit of the binger in her, but she really went into high gear on the binging at that point in her life and has remained there. She is very critical of anyone else spending money on anything, but she can go out and spend several thousand dollars (that she supposedly didn't have a week earlier) on new furniture, diamond rings, or whatever she has decided she needs to maintain her status at the moment. My Dad is pretty much a miser and as long as he has some money in his pocket, he doesn't care what she does most of the time. This is pretty difficult for me because I'm not money motivated, but I take care of it the best I can. One of my brother's is just a spender (so is his wife) and mother has bailed them out over &amp; over. My other brother is a miser like Dad with a little of the spender characteristics, and his wife is a hoarder with spender characteristics. I believe that if it is necessary to spend some money for health care or something like that, then do it. They won't. If two items are nearly the same, but the prices are widely apart, go for the cheaper one (Mom, their wives, &amp; both brothers would buy the brand name if it was for themselves, but a cheaper model for someone else.)They will cheat if they get the chance, but profess to be honest. I will tell the clerk if they undercharged me or gave me too much change. They say I'm too honest. I get totally frustrated with the money wars and try to point out to all of them that you can't take it with you and family is more important than money, so I end up the bad guy most of the time. I'm tired of all of them. To make matters worse, I'm the POA and executor of our parents' estate. They are both elderly and ill. I figure it's going to get real ugly and I don't know how to stop it. </description>
      <author>JeanC</author>
      <pubDate>Fri, 10 Jul 2009 02:58:01 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-prevent-family-money-conflicts-by-reconciling-money-styles</guid>
      <link>http://www.caring.com/blogs/how-to-prevent-family-money-conflicts-by-reconciling-money-styles/comments</link>
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      <title>Comment on Beware Red Meat, the New Cancer Risk</title>
      <description>Here's a link to the abstract: http://glycob.oxfordjournals.org/cgi/content/abstract/cwn072. But this is just one study focusing on the mechanism; there have been numerous studies on red meat, processed meat, colon cancer, and pancreatic cancer and my point was to try to pull it all together as a health alert.</description>
      <author>Melanie Haiken</author>
      <pubDate>Thu, 09 Jul 2009 22:39:10 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/newslflash-eating-red-meat-raises-cancer-risk</guid>
      <link>http://www.caring.com/blogs/newslflash-eating-red-meat-raises-cancer-risk/comments</link>
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      <title>Comment on Beware Red Meat, the New Cancer Risk</title>
      <description>What ball park do you go to?  Here you cannot bring in any food or beverage.  Something about safety?</description>
      <author>thevanman</author>
      <pubDate>Thu, 09 Jul 2009 18:18:13 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/newslflash-eating-red-meat-raises-cancer-risk</guid>
      <link>http://www.caring.com/blogs/newslflash-eating-red-meat-raises-cancer-risk/comments</link>
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      <title>Comment on Why Hospitals and Alzheimer's Are a Tough Mix</title>
      <description>Thanks, now I understand my mom strange behaviour. This is very informative article. My mom is now hard to sleep, any one can explain this phenomenon?</description>
      <author></author>
      <pubDate>Thu, 09 Jul 2009 01:36:17 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/why-hospitals-and-alzheimers-are-a-tough-mix</guid>
      <link>http://www.caring.com/blogs/why-hospitals-and-alzheimers-are-a-tough-mix/comments</link>
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      <title>Comment on Beware Red Meat, the New Cancer Risk</title>
      <description>To put 'consumption of red meat and processed meat' in the same sentence, on equal footing, is not correct science. Do you happen to have a citation for the actual study (you only link to Science Daily's interpretations of the study.) As a scientist, I'd like to read the original report. Could you publish the link, so that all could follow it?</description>
      <author>Anonymous</author>
      <pubDate>Wed, 08 Jul 2009 16:15:03 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/newslflash-eating-red-meat-raises-cancer-risk</guid>
      <link>http://www.caring.com/blogs/newslflash-eating-red-meat-raises-cancer-risk/comments</link>
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      <title>Comment on Why Hospitals and Alzheimer's Are a Tough Mix</title>
      <description>My Dad was in the hospital last year right when he was beginning to show signs of dementia. I wondered why he kept insisting he was in a hotel and why he accidentally pulled out his catheter. Now I know. Thanks.</description>
      <author>IrishMiddleChild</author>
      <pubDate>Wed, 08 Jul 2009 15:45:10 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/why-hospitals-and-alzheimers-are-a-tough-mix</guid>
      <link>http://www.caring.com/blogs/why-hospitals-and-alzheimers-are-a-tough-mix/comments</link>
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      <title>Comment on Dementia Alert: The Scary Complication Nobody Tells You About</title>
      <description>Yes, I was not prepared for the many months of delirium my mother had during a hospital and rehab stay for a broken hip. I was getting used to her dementia and forgetfulness (answering the same question every 30 seconds... sound familiar?) but her violence, delusions, hallucinations, screaming, accusations, paranoia, etc. really threw me. She claimed to have talked to deceased relatives, claimed people had visited her (they hadn't), asked how her mother was doing (who had died 12 years ago at age 98!), thought she was in a hotel one day, the next day she thought she was at her beauty salon because a nurse resembled her hair stylist, screamed at me for not letting her leave, cried, threw tantrums, or wouldn't speak to me at all, crawled under the bed looking for her purse, tried to stab medical personnel with eating utensils, and on and on. It was a nerve shattering experience and I felt so helpless because I couldn't do anything to make it better or settle her down. Even the nursing staff said it was the worst they'd ever dealt with and seemed ill-equipped to deal with her mental issues. Now that she's somewhat recovered (10 months later) she fortunately has no memory of any of that, but it is ingrained in my head and I worry about the next hospital stay she'll have! It is so incredibly difficult and they do have the advantage of forgetting all the bad stuff. But the caregiver has to whether the storm and deal with the memory of it. I think there's going to be an epidemic of caregiver fallout health-wise both mentally and physically. Add to that stress the current economical mess. Very trying times.</description>
      <author>doforanimals</author>
      <pubDate>Tue, 07 Jul 2009 18:28:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-alert-the-scary-complication-nobody-tells-you-about</guid>
      <link>http://www.caring.com/blogs/dementia-alert-the-scary-complication-nobody-tells-you-about/comments</link>
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      <title>Comment on Take the New 5-Minute Alzheimer's &quot;Test&quot; &#8211;- And Then Do This</title>
      <description>Same problem as flyguy: I was unable to enter answers into the test area. However, I did the questions in my head (except for the one about the prime minister).</description>
      <author>Anonymous</author>
      <pubDate>Tue, 07 Jul 2009 06:18:28 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/take-the-new-5-minute-alzheimers-test-and-then-do-this</guid>
      <link>http://www.caring.com/blogs/take-the-new-5-minute-alzheimers-test-and-then-do-this/comments</link>
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      <title>Comment on Take the New 5-Minute Alzheimer's &quot;Test&quot; &#8211;- And Then Do This</title>
      <description>I was unable to enter data into the test area. Was not allowed by the program to do so.
</description>
      <author>flyguy1934</author>
      <pubDate>Mon, 06 Jul 2009 21:13:23 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/take-the-new-5-minute-alzheimers-test-and-then-do-this</guid>
      <link>http://www.caring.com/blogs/take-the-new-5-minute-alzheimers-test-and-then-do-this/comments</link>
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      <title>Comment on &quot;One Day at a Time&quot; and 4 Other Caregiver Stress Coping Traps to Avoid</title>
      <description>This article is really an eye opener, particularly the last trap. Before my dad died I promised him that I would take care of my mom. My husband and I have taken care of my mom for 6 years in our home. She doesn't have Alzheimer's but does have some dementia. As her other health problems increase, plus the dementia, it is getting more difficult to keep that promise. I'm starting to think that a nursing home might be the better option, but feel so guilty even thinking about this. I just want what is best for her care.  This is the hardest thing I have ever done in my life.</description>
      <author>Anonymous</author>
      <pubDate>Sat, 04 Jul 2009 00:54:58 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/one-day-at-a-time-and-4-other-caregiver-coping-traps-to-avoid</guid>
      <link>http://www.caring.com/blogs/one-day-at-a-time-and-4-other-caregiver-coping-traps-to-avoid/comments</link>
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      <title>Comment on 5 Money Styles and How Differences Cause Family Conflicts </title>
      <description>Hi Claire, I think you're right, there is a Depression-era combination of worrier and hoarder that is particularly challenging, and many of our parents fall into this demographic. My mother was similar; I had to redo her budget over and over to try to prove to her that she had enough money to pay a caregiver a few hours a week and give my sisters and me some respite. Good luck with your situation!</description>
      <author>Melanie Haiken</author>
      <pubDate>Fri, 03 Jul 2009 00:46:22 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/5-money-styles-and-how-differences-cause-conflict-in-families</guid>
      <link>http://www.caring.com/blogs/5-money-styles-and-how-differences-cause-conflict-in-families/comments</link>
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      <title>Comment on &quot;One Day at a Time&quot; and 4 Other Caregiver Stress Coping Traps to Avoid</title>
      <description>Two years ago my husband and I relocated to live with my mom.  Four years ago my dad passed away.  Mom has had breast cancer, heart failure and is practically blind because of glaucoma.  I have one brother that lives here but does not help at all in fact he doesn't even speek to me because he thinks I want her &quot;money&quot;. We took a financial loss moving here and I work prn at a hospital. We will both be getting equal shares after her death and it really isn't that much money.  I really feel so alone in this because I hate to complain to my husband because he is so understanding of the situation.
This blog really helps put the stress in prospective.</description>
      <author>Anonymous</author>
      <pubDate>Thu, 02 Jul 2009 19:33:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/one-day-at-a-time-and-4-other-caregiver-coping-traps-to-avoid</guid>
      <link>http://www.caring.com/blogs/one-day-at-a-time-and-4-other-caregiver-coping-traps-to-avoid/comments</link>
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      <title>Comment on Is There Such a Thing as a &quot;Caregiving Instinct&quot;?</title>
      <description>I think there is,  my Mom says I was caring for someone when I was little.  I have cared for my grandparents and now my parents.  </description>
      <author>Jaye</author>
      <pubDate>Wed, 01 Jul 2009 18:00:00 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-there-such-a-thing-as-a-caregiving-instinct</guid>
      <link>http://www.caring.com/blogs/is-there-such-a-thing-as-a-caregiving-instinct/comments</link>
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      <title>Comment on 5 Money Styles and How Differences Cause Family Conflicts </title>
      <description>There is one category missing.  My parents are children of the depression (b. 1921).  The are a very difficult combination of Worrier and Hoarder.  They have plenty of money (enough to live in the facility they are in for 25+ years, and it is a land-locked cruise ship-type), yet they wear shoes until they have holes in the soles.  They purchase clothes only once every 5 years or so, and the clothes they purchase are Walmart or 'dollar' store clothing.  Very frustrating to us kids.  When we moved them, we had to give to junk stores and throw out a very large amount of 'precious' items.  They are still asking where something is (cost in 1960 $5.00, worn out and dirty).</description>
      <author>CA-Claire</author>
      <pubDate>Wed, 01 Jul 2009 14:37:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/5-money-styles-and-how-differences-cause-conflict-in-families</guid>
      <link>http://www.caring.com/blogs/5-money-styles-and-how-differences-cause-conflict-in-families/comments</link>
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      <title>Comment on Dementia Alert: The Scary Complication Nobody Tells You About</title>
      <description>After my husband had six major surgeries, a few trips to the emergency room, C-Diff infection, in-patient therapy and finally, cardiac arrest in 2008 followed by another month-long in-patient therapy, I feel qualified to add a few things. My husband was in two hospitals. The doctors didn't seem to be talking to each other. Nursing staff at one hospital were constantly in his room because of vomiting and diarrhea. I requested he be moved to Intermediate Care. My husband would not look at me, talk to me, spit on me, etc. He became combative and had to be restrained. I kept telling them to look at his sodium level. What do I know? One nurse told me that he had seniority--I corrected him by saying that we had been married 45 years, and I had 45 years seniority! My husband was having gall bladder attacks that were not recognized, until I insisted he be examined. On and On. We made it home, only to have infection settle in his right knee replacement (June). Back to the hospital on emergency basis. Different doctors, different hospital. Better care. Still C-Diff. Knee surgery (6th for year). Released December 1. Follow-up for infection control. Cardiac arrest at home December 5. ICU. Lowered body temperature. Induced coma. I agree that if you are not with your patient almost 24 hours a day, things can get out of hand. You have to insist that you know what you're talking about. Even argue with a doctor if necessary. He/she may be part of a group and is &quot;doing rounds&quot; for your main doctor. Specialties disagree on meds. Your mother is blessed to have you to look after her. BUT--if she is hospitalized again, make sure they check her sodium level! Best to all of you. Oh, by the way, my husband came home with little brain damage and is doing fine now. Thanks to an excellent EMS team who were only 4 minutes away.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 30 Jun 2009 21:44:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-alert-the-scary-complication-nobody-tells-you-about</guid>
      <link>http://www.caring.com/blogs/dementia-alert-the-scary-complication-nobody-tells-you-about/comments</link>
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      <title>Comment on Don't Have Health Insurance? Here's How to Get Health Care Anyway</title>
      <description>This is great for low income, but what about a person whose company discountinued coverage one week and the employee was rushed to the hospital the next week with an unknowned brain tumor?  This person is now uninsurable with a pre-existing condition.  That was 4 years ago and still has not had the needed surgery.</description>
      <author>sdhIndy</author>
      <pubDate>Tue, 30 Jun 2009 18:59:00 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dont-have-health-insurance-heres-how-to-get-health-care-anyway</guid>
      <link>http://www.caring.com/blogs/dont-have-health-insurance-heres-how-to-get-health-care-anyway/comments</link>
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      <title>Comment on RIP Farrah Fawcett, Who Wanted Us to Take Her -- And Cancer -- Seriously</title>
      <description>I hear fighting cancer so many times,Big John Wayne Beautiful Farrah Plucy Wendy Ricards and Jade,it is so stressful,stress and cancer seem to go together I have had cancer for 7 years I have never fought it,I am too big a coward I just to relax as much as possible and give my imune system a chance to do its job,it has had a million years of experience.of course I could be just an old fool,but I have avoided all pain and trauma that fighting cancer brings.I remain a live coward.I admire the fighters,but I cannot follow them.</description>
      <author>octoman</author>
      <pubDate>Tue, 30 Jun 2009 16:04:25 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/rip-farrah-fawcett-who-wanted-us-to-take-her-and-cancer-seriously</guid>
      <link>http://www.caring.com/blogs/rip-farrah-fawcett-who-wanted-us-to-take-her-and-cancer-seriously/comments</link>
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      <title>Comment on What Michael Jackson's Early Death Can Teach Us About Heart Health</title>
      <description>i have a history of high blood pressure,and is on meds to control it,but sometimes i forget to take them.since M.J. death its a wake up call for me to take my meds every single day.</description>
      <author>debbie darville</author>
      <pubDate>Sun, 28 Jun 2009 17:47:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/as-we-mourn-michael-jackson-dead-of-cardiac-arrest-at-50-we-need-to-protect-our-own-hearts</guid>
      <link>http://www.caring.com/blogs/as-we-mourn-michael-jackson-dead-of-cardiac-arrest-at-50-we-need-to-protect-our-own-hearts/comments</link>
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      <title>Comment on What Michael Jackson's Early Death Can Teach Us About Heart Health</title>
      <description>Michael is not the youngest of the Jackson's brothers.  Info was helpful</description>
      <author>Anonymous</author>
      <pubDate>Sat, 27 Jun 2009 12:59:23 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/as-we-mourn-michael-jackson-dead-of-cardiac-arrest-at-50-we-need-to-protect-our-own-hearts</guid>
      <link>http://www.caring.com/blogs/as-we-mourn-michael-jackson-dead-of-cardiac-arrest-at-50-we-need-to-protect-our-own-hearts/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>My heart goes out to anyone who is not appreciated for the efforts that they extend to an aging parent. My father has dementia. My sister lives in Oregon. She and I have always been polar opposites since birth. Our mother became ill with ovarian cancer 8 years ago and during the last phase of her illness my sister visited her and convinced her to make a change to my parents Living Trust documents and give her the right of first refusal to purchase all of the family land ahead of me. Our parents attorney, my father, mother, sister and brother in law all knew that this document had been created. I found out, six months after my mother died. My father told me about the document, said he did not agree with it and he had never signed it. Eventually he told my sister and her husband that he was not going to sign it. Now our father has dementia. I live in the same town and see him daily. He also has two wonderful care givers that are with him for 2 hours a day 7 days a week.  He does not cook, clean, do his laundry and needs help with his medication each day. He lives alone. My greatest concern is his safety, both physically and financially. He became adicted to sending money to fraudlent companies and was placed on the Super Sucker List!. This has been going on since our mother died. One summer he deposited 4 counterfiet checks into his Trust checking account. The bank VP had me bring my Dad to her office to discuss these checks and asked him to stop writing them to the fraudlent organizations. He did not. I was then asked to have his primary care physician write a letter to his bank addressing his medical condition and whether he should be writing any checks. His physician informed the bank officials that Dad had dementia for several years and that he should not be writing checks without a second signature power of attorney from one of his daughters, namely me. I received a call from his Trust attorney, who by the way owns the bank where he has banked for 80 years, is the President of the bank and the attorney for the bank. He wanted me to bring Dad to his office for a talk. I did and for one hour his attorney asked Dad 7 different times to step down as Trustee of his Trust and let my sister and I do our jobs as co-trustee's. Dad refused each time. His attorney brought up the letter that they had requested from his physician and his memory loss and confusion. Dad continued to refuse. There was no provision made to stop him from continuing to write checks. I received a letter from his attorney memoralizing our meeting and the fact that Dad did not want to step down as trustee of his Trust. I was told to hire my own attorney to make that happen. This was July of 2007. In May of 2008 the same Trust attorney began to change Dad's Trust documents and notorize his signature. My sister started making trips to visit our father when she knew that I would be out of town. She took him to a new attorney, had me removed as Power of Attorney on his bank account, so I could no longer pay his bills for him. The new attorney created a document that removed both my sister and me as co-trustee's of our father's Trust and named himself as successor Trustee and then personally notorized our father's signature. This new attorney is the law partner of his Trust attorney. He had all the medical documentation that Dad had dementia and did not have the capacity to understand and should not be changing any legal documents that were created prior to his diagnosis of dementia. My sister thinks that Dad is &quot;fine&quot; he has no memory problems. When Dad was visiting her in Oregon she took him off of his Aracept that his Neurologist in San Francisco had put him on months before and was doing great on. She said, &quot;It is safer for Dad to have a worse memory than to be on medication for it.&quot; She also believes that, &quot;The body will heal itself.&quot; She will not volintarily have a family meeting with a mediator. We can not come to an agreement on anything related to keeping our father safe. I finally had a consultation with an attorney about Conserving our father. I found out that my sister, brother-in-law and father all went to Dad's Trust attorney and they were making yet another Amendment to the Family Trust and this would give my brother-in-law Durable Power of Attorney over all our father's wealth. That was the straw that broke the camels back, so to speak. I hired the attorney to Conserve my father. He was offically served the documents for a hearing in July and he promptly had someone drive him to those special attorney's affiliated with his bank and Trust and told them he did not understand what the papers ment and needed their help. The very same attorney's that are part of the reason necessary to Conserve him are now involved tryng to keep me from doing that. When family members and attorney apply undue influence on my Dad, the only thing left to do is try to stop them. It is a very emotional process. My father thought that I was suing him and that I didn't like him any more. It broke my heart to hear him say that. I told him I was not suing him and that this was being done to protect him and reduce some of the stress that he was being subjected to. He still does not understand. My adult children are very upset with their Aunt.  They see their grandfather often and see his dementia in action. It is very sad for all concerned. Again, my heart goes out to  all of you who are having difficulties with sibblings that believe something other than reality, and live far away from the parent with special needs that you are caring for. Do what you have to do and know that there are those of us who support you all the way.
JLN</description>
      <author></author>
      <pubDate>Thu, 25 Jun 2009 20:26:33 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on Do Parents With Dementia Need a &quot;Sexual Power of Attorney&quot;?</title>
      <description>Dad wants Mom to have oral sex and she is not into it at all.  Is the only solution for him to relieve himself in the shower?
</description>
      <author>Anonymous</author>
      <pubDate>Wed, 24 Jun 2009 21:43:57 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/do-parents-with-dementia-need-a-sexual-power-of-attorney</guid>
      <link>http://www.caring.com/blogs/do-parents-with-dementia-need-a-sexual-power-of-attorney/comments</link>
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      <title>Comment on How to Make Difficult Conversations Less Stressful</title>
      <description>My Dad cares for Mom and they live in the first floor of my house.  I try to keep their home clean and fresh, but Mom is always cold so Dad won't put the air on or a fan.  The place has a musty smell from cooking and humidity and I keep telling him to circulate air but either forgets or he ignores me because she's cold. I don't know what else to do.</description>
      <author>Anonymous</author>
      <pubDate>Wed, 24 Jun 2009 20:02:20 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful</guid>
      <link>http://www.caring.com/blogs/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful/comments</link>
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      <title>Comment on 3 Key Steps to Protect Against Falls -- and Prevent a &quot;Cascade&quot; of Health Problems</title>
      <description>I am a physical therapist with over 20 years in long term care.  The bulk of my case load deals with fall prevention.  Here are some basic environmental tips--
1. get rid of throw rugs
2. get rid of clutter--as we age, &quot;less is more&quot;
3. use night lights
4. consider a bedside commode for urgency during the night--people who hurry tend to fall
5. many older folks use 25 watt bulbs to save money--they already have compromised vision--low light can contribute to confusion about shadows/shapes on the floor, leading to falls
6. check shoes/slippers--if they fit poorly, they can contribute to a fall
7. avoid &quot;lift chairs&quot; and other aids that make life &quot;easier&quot;--they also make muscles weaker, eventually leading to a fall.  All adaptive equipment should be evaluated for the individual person, not just used because it's available--consult a PT with experience in long term care
8. Strengthening the trunk and lower extremities is key--maintaining good range of motion is important--avoid sleeping with pillows under the knees--it leads to stiff knees and ankles.  If anything, pillows are used under the calves, to keep pressure off the heels.  For people who move freely, I'd stick to no pillows.
I love working on fall prevention.  Hope some of these tips are helpful!
Sunshine</description>
      <author>Anonymous</author>
      <pubDate>Tue, 23 Jun 2009 21:40:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/3-key-steps-to-protect-against-falls-and-prevent-a-cascade-of-health-problems</guid>
      <link>http://www.caring.com/blogs/3-key-steps-to-protect-against-falls-and-prevent-a-cascade-of-health-problems/comments</link>
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      <title>Comment on 3 Key Steps to Protect Against Falls -- and Prevent a &quot;Cascade&quot; of Health Problems</title>
      <description>These are wonderful ideas! Thanks so much and i'll be sure to write about them in future posts. Really appreciate your feedback.</description>
      <author>Melanie Haiken</author>
      <pubDate>Tue, 23 Jun 2009 18:39:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/3-key-steps-to-protect-against-falls-and-prevent-a-cascade-of-health-problems</guid>
      <link>http://www.caring.com/blogs/3-key-steps-to-protect-against-falls-and-prevent-a-cascade-of-health-problems/comments</link>
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      <title>Comment on 3 Key Steps to Protect Against Falls -- and Prevent a &quot;Cascade&quot; of Health Problems</title>
      <description>My mother has vascular dementia and possibly Alzheimer's disease, and when she fell and fractured her pelvis two years ago, the physical therapist at her rehab center suggested HipSavers--a girdle-like garment you wear under your pants, with three soft disc pads built in, one pad in the back over the tailbone and one on each hip. Mom has been wearing them since she recovered from her fracture, and though she's been found on the floor of her memory care facility a few times (she forgets to use her walker), she has had no more injuries. Some people object to wearing them, but in my mother's case she does not, as she forgets she has them on. If falling is a concern, and you want to avoid your loved one having to spend weeks or months in the hospital and rehab, I highly recommend HipSavers. They're fairly new, but you can find them online.  </description>
      <author>Martha</author>
      <pubDate>Tue, 23 Jun 2009 13:23:01 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/3-key-steps-to-protect-against-falls-and-prevent-a-cascade-of-health-problems</guid>
      <link>http://www.caring.com/blogs/3-key-steps-to-protect-against-falls-and-prevent-a-cascade-of-health-problems/comments</link>
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      <title>Comment on 3 Key Steps to Protect Against Falls -- and Prevent a &quot;Cascade&quot; of Health Problems</title>
      <description>There are many missing pieces in fall prevention efforts. For example: A recent study published in the Journal of Clinical Nursing showed that 1 in 6 older people who lived at home were under-nourished and at risk of malnutrition. Low levels of certain minerals can cause dizziness and balance problems. Another report showed vitamin D helped reduce falls. It&#8217;s hard to get strength or balance if you lack the nutrients that help improve either problem. Another issue is how drugs deplete certain nutrients. This is an area that gets too little attention.

A research report in the January 2009 Journal of American Geriatrics Society showed a lack of effect of Tai Chi had on preventing falls. Then there is another that says exercise is good. No doubt exercise is beneficial but it seems everyone needs to be properly assessed to make sure the benefits out weigh the risks. The CDC focuses on exercise and overlooks bed falls while statistics show it is an issue. The statistic below is from the CDC:

Difficulty performing activities of daily living among Medicare beneficiaries, ages 65+: US, 2006 figures: Non-institutionalized 

Getting In/Out of Bed/Chair 	11.9%
Using Toilet 		4.8%

We have big gaps in getting important information out about falls causes. Too many programs rely on those who are not well informed about leading causes of falls and fall deaths or how to prevent them. According to the National Safety Council (nsc.org) falls from bed are the second leading cause of fall death after stairs and steps. Here is the web address for the quiz: http://nsc.org/resources/issues/falquiz.aspx 

Device safety in fall prevention programs are another area of concern where the focus is on cheap cost not safety or effectiveness. Too many devices are not used as intended while the recommenders don't know the intended use. We have a long way to go in fall prevention this includes educating the educators.
</description>
      <author>Patrece Banks</author>
      <pubDate>Mon, 22 Jun 2009 15:25:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/3-key-steps-to-protect-against-falls-and-prevent-a-cascade-of-health-problems</guid>
      <link>http://www.caring.com/blogs/3-key-steps-to-protect-against-falls-and-prevent-a-cascade-of-health-problems/comments</link>
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      <title>Comment on How to Make Difficult Conversations Less Stressful</title>
      <description>Okay, now I don't feel so bad!  I'm working with a 81 year-old mother who is in and out of situations which cause me concern, and I've backed off because  don't want to deal with the vicious responses.  I know now that it doesn't matter how she responds...I have to create a positive conversation if I can.  THANK YOUU</description>
      <author>jjobse</author>
      <pubDate>Sun, 21 Jun 2009 06:44:24 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful</guid>
      <link>http://www.caring.com/blogs/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful/comments</link>
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      <title>Comment on How to Make Difficult Conversations Less Stressful</title>
      <description>Very informative and helpful article.  I just want to add another dimension to painful conversations with our parents.  What if you have a parent that has been a rageaholic all their lives?  If you bring up any topic that is sensative, a rageaholic parent will make you pay the rest of your days.  I understand wanting to keep them safe and protected as well as others, but I also know from experience that self-preservation is also very important.</description>
      <author>Anonymous</author>
      <pubDate>Sat, 20 Jun 2009 23:03:27 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful</guid>
      <link>http://www.caring.com/blogs/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful/comments</link>
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      <title>Comment on How to Care for Someone Who Has Cancer - AND a Negative Attitude</title>
      <description>...9:15 AM EST...yeah right...&quot;beckiecann&quot;...you need to identify yourself if you're going to play &quot;pretend doctor&quot;...while you're telling cancer patients and/or their relations you have &quot;something far worse than cancer&quot; to justify your rambling. As you say, you &quot;don't have cancer&quot;, so you need to get off this blog and a see a &quot;Gulf War&quot; shrink, because I suspect you're enjoying your &quot;Gulf War Illness&quot; a little too much...J.B. 6/20/09</description>
      <author>James Ballard</author>
      <pubDate>Sat, 20 Jun 2009 13:31:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude</guid>
      <link>http://www.caring.com/blogs/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude/comments</link>
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      <title>Comment on Take the New 5-Minute Alzheimer's &quot;Test&quot; &#8211;- And Then Do This</title>
      <description>i am forgetful but all my friends tell me the same thing, but i would like to find out the truth.</description>
      <author>joskutay</author>
      <pubDate>Sat, 20 Jun 2009 12:37:11 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/take-the-new-5-minute-alzheimers-test-and-then-do-this</guid>
      <link>http://www.caring.com/blogs/take-the-new-5-minute-alzheimers-test-and-then-do-this/comments</link>
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      <title>Comment on How to Make Difficult Conversations Less Stressful</title>
      <description>this is one of those articles i'll file for future reference.  thanks. -karen</description>
      <author>Anonymous</author>
      <pubDate>Sat, 20 Jun 2009 11:28:40 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful</guid>
      <link>http://www.caring.com/blogs/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful/comments</link>
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      <title>Comment on How to Care for Someone Who Has Cancer - AND a Negative Attitude</title>
      <description>I shuddered as I read this blog. I don't have cancer. I have something far worse - Gulf War Illness. The &quot;depression&quot; is an effect of the destruction taking place at the cellular level by both chemo and cancer. Anti-depressants, anti-anxiety meds will absolutely aggravate symptoms of fatigue and irritability.
      Anti-depressants depress the immune system so much by making the cancer patient more prone to opportunistic infections, fungal overgrowth, and bacterial infections of the intestine. And if a chemo patient is suffering insomnia, it means their adrenals are bad shape. They are not producing sufficient levels of cortisol, which is produced only during deep sleep. Most sleep medications do not sedate sick people long enough to provide deep, refreshing sleep, much less produce sufficient cortisol.
    Exhaustion sleep or debilitating chronic fatigue that chemo triggers is hardly ever refreshing.
For Gulf War Illness, I rely on several adrenal hormones - bio-identical or nutriceuticals - to pick me up off the bottom of the well, face-down in the mud. As far as I can tell, I have never been clinically depressed. The biomarkers for depressed people is over-production of cortisol. They usually have belly fat from being stressed, producing too much cortisol. You don't see that on cancer patients.
     Also, a much better way to beat cancer is by IV infusion therapy of Vit C or extremely diluted H2O2 (pharmaceutical grade hydrogen peroxide) in a small bag of dextrose. Anyone whose system is being depleted by disease should always consider the Myer's Cocktail IV infusion therapy. It replenishes minerals and nutrients at the cellular level, where chemo strips the system at a cellular level.
    Irritability may also be hormone imbalance, especially if losing weight and losing hair. A very, very good adrenal-pituitary supplement is Pregnenalone. You can not take so much of it that it is dangerous. The best kind is sublingual tablets you can find a natural foods market or pharmacy. The tablets dissolve under the tongue, by-pass blood-brain barrier and provide instant relief. Grumpiness is instantly gone. For me, Pregnenalone relieves mid-back pain of adrenal inflammation. www.prohealth.com has a product called Adrenal Support, extremely helpful when diet is running straight through or coming back up quite often.
    I encourage everyone to understand how important educating yourself about chemo-therapy and how devastating it is to the entire system. Some forms of chemo actually cause rapid-growing cancer. So learn how to rebuild nutritionally at the cellular level before you start rolling out prescription mind-numbing, mood-altering drugs that enhance the devastation.</description>
      <author>beckiecann</author>
      <pubDate>Sat, 20 Jun 2009 06:51:53 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude</guid>
      <link>http://www.caring.com/blogs/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude/comments</link>
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      <title>Comment on How to Make Difficult Conversations Less Stressful</title>
      <description>Thanks all for your input. I love that pullups story! And Anonymous, I hope you'll look for some caregivers in similar situations with relatives in our discussion groups (click &quot;Groups&quot; above) -- more people than you know can relate to your hardship, and may have other supportive insights for you --</description>
      <author>Paula Spencer</author>
      <pubDate>Sat, 20 Jun 2009 01:36:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful</guid>
      <link>http://www.caring.com/blogs/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>That's a turnaround.  Could she be living the life of a martyr and feel she has to do everything herself?  Does she have control issues?  (I know I've been accused of that, but that's not possible when I'm asking for help.)  Does the caretaker have a friend/neighbor/clergy that could try to find out for you?  Could the parents arrange something?  POA can be over-ridden with a judgement of guardianship through the court if you feel you need to go that far.  

The problem is that when one person won't communicate, the door is closed.  I don't know what else you could do.  My prayers are with you &amp; your family.</description>
      <author>sttng</author>
      <pubDate>Fri, 19 Jun 2009 19:55:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Don't Have Health Insurance? Here's How to Get Health Care Anyway</title>
      <description>These are great suggestions.  They can work for young and old.</description>
      <author>dihi</author>
      <pubDate>Fri, 19 Jun 2009 18:08:01 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dont-have-health-insurance-heres-how-to-get-health-care-anyway</guid>
      <link>http://www.caring.com/blogs/dont-have-health-insurance-heres-how-to-get-health-care-anyway/comments</link>
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      <title>Comment on How to Make Difficult Conversations Less Stressful</title>
      <description>This is one of the best articles I have read.  Very practical and right on point.  In a keynote I gave yesterday, I talked about the very same thing and the need to find you power.  We need to be strong to address these issues, but it is a absolute necessity. On this long journey there are indeed &quot;ages and stages&quot;.  And thank you Rob for that funny story which brought humor and solution to the problem. </description>
      <author>Joy Golliver</author>
      <pubDate>Fri, 19 Jun 2009 14:31:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful</guid>
      <link>http://www.caring.com/blogs/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful/comments</link>
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      <title>Comment on How to Make Difficult Conversations Less Stressful</title>
      <description>Paula, you're doing a terrific job answering these caregiving questions from frustrated relatives! I wanted to say that most of them would benefit, I think, from support group meetings, even if they have to pay someone to be with their care recipient during that time. 
I learned so much, from the young man who solved his problem with pullups for the incontinent father who simply would not accept the idea: the son took off his pants, put on a set of pullups, got his father to do the same, and after a while they looked at each other and laughed. That broke the ice - the barrier so many close relatives and spouses have in caregiving. There is no intimacy like the caregiving intimacy, and shame and embarassment have to be put aside in order to make things work. </description>
      <author>Rob</author>
      <pubDate>Fri, 19 Jun 2009 13:45:36 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful</guid>
      <link>http://www.caring.com/blogs/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>What about the siblings who don't live near the parents or caretaker who have asked for family conferences to determine roles and responsibilities and get no answer from the caretaker?  We are willing to take on what we can from a distance, but my sister refuses to acknowledge this or to discuss it -- she'd rather complain.  And yet she tells my parents she's too busy to check on a financial account, for which she gets all the statements.  I know it is not easy for the caretaker and I have made trips to relieve her -- but the caretaker, especially if she/he has POA, owes the other siblings updates, expecially when asked.  If the caretaker refuses to respond to phone calls, emails and letters, what can be done?</description>
      <author></author>
      <pubDate>Thu, 18 Jun 2009 16:12:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>I am the primary caregiver for a brother.  Fortunately, I have the support of my husband, other brother and mother.  However, my sister - who happens to live in Denmark and had had power of attorney for our disabled brother - threw a major hissy fit over me having power of attorney and then needing to persue legal guardianship.  She has it in her head that she could manage his care from overseas through e-mail and phone calls.  She has said many hurtful things to me about the situation and is of no help whatsoever.  She believes she is in the right and knows what is best for him although she cannot be her to attend to his needs.  It has hurt me deeply but also given me a chance to think back over the years about her behavior on other things and realize that she's always been this way.  In spite of her actions, I have tried to take the high road and keep the lines of communication open.  She has a laundry list of reasons why I shouldn't be the caregiver/guardian including &quot;I promised Dad when he was so sick that I would care for Tim and now I have to break my word and that pains me more than you'll ever know.&quot;  She manages to always make it about her.  Each time I extend the olive branch it's slapped away.  While my mother is alive, I will continue to try to patch things up and keep her up to date on family happenings.  I look at it this way, she has to live with her choices and face up to what she's done at some point.  She isn't her to help with her mother, who is also in need of care and attention, and makes few attempts to contact her either.  Have come to realize that I have to do what's right for me, having the support of the rest of the family helps termendously.  Learning to accept that (her words, not mine) she hates me and know that I'm doing the right thing regardless of what she thinks.  But this has put a large strain on our family's relationship with her and it's very sad.  Trying to move on but it's easier said than done.</description>
      <author>ebiden</author>
      <pubDate>Thu, 18 Jun 2009 13:48:36 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on How to Make Difficult Conversations Less Stressful</title>
      <description>i am taking care of my mother at my home,she has end stage liver diesease and advanced dementia and brain damage.she has to have her diapers changed ,bathed fed, supervised 24 hours a day.my father died almost two years ago from cancer and he and my mother wanted me to be her power of attorney.well she was staying in a nursing home for 5000.00 a month and i didn't like the way they cared for her as much as i thought i could.i needed a job also (i knew it would be hard caring for her and being p.o.a. but she has been here for 9 months now.so i decided to bring her home, but also instead of paying a nursing home i would pay myself half of what she was paying from my fathers pension and social security.My brother was living at my dad and moms house when he passed but my father kept telling me to sell the house and the 3 children (us) would share the money .but my brother says he cant pay rent since he really wanted to keep living there and so i said either pay rent or i will sell the house.well 2 years later not one cent has been paid he was supposed to give my sister and me half of the renteach month.now my sister and husband are having hard times and she &quot;says&quot; she wants half the money i make so i said fine we can take turns a week or  two at a time.Now she says she cant do it at her house so she will take her to my brothers house and watch her there except she wanted to go home at night and come the next afternoon and stay till she goes to sleep.I told her i didn;t think that that was right i thought she should spend the night also cuz mom wanders around alot at night plus my sister in law is having a baby in 4 days.she got all put out and acts like i am ripping my mom off!! When neither of my siblings rarely come visit her here except x-mas b-days etc.She my sister says she feels like shes not getting anything since my brother dont pay rent and i get paid for caring for her and buying diapers ,wipes ,clothes,baby food or pureeing everything she eats.And she thinks after my dad died my mom is still getting the full retirement they were getting bt after he passed she gets an annuity which is half of that.I really feel hurt by her comments i told her call the pension plans ans soc. security to see how much she gets.anyways things sure get out of hand and all they keep asking is if i could get money out of her cd's my grandmother and my mom had together but i explain to them thats my moms money until she pases then we are the benificeries I CANT BELIEVE THIS!!!</description>
      <author>Anonymous</author>
      <pubDate>Thu, 18 Jun 2009 08:02:42 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful</guid>
      <link>http://www.caring.com/blogs/how-make-a-difficult-conversation-with-an-aging-parent-less-stressful/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>It's so unbelieveable, isn't it?  I sent several &quot;updates&quot; over the course of 5 years with silence as the answer.  When I asked, they'd say they didn't receive it (my sister's husband intercepts mail from me, which is a federal offense) or had gotten it but hadn't read it yet.  The niece that asked for in scolded me with various emails about how all this tension isn't good for Grandma &amp; how one person shouldn't have to be responsible for all care - that was then.  Now she's blaming &amp; accusing and STILL not helping.  

GOOD LUCK!</description>
      <author>sttng</author>
      <pubDate>Wed, 17 Jun 2009 21:51:10 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Take the New 5-Minute Alzheimer's &quot;Test&quot; &#8211;- And Then Do This</title>
      <description>You didn't miss anything, and deserve extra points for good attention!...I didn't realize the scoring wasn't on the score page I linked to. So I've added this info (from reports on the test) within the post as an &quot;update&quot; above. thanks!</description>
      <author>Paula Spencer</author>
      <pubDate>Wed, 17 Jun 2009 20:04:51 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/take-the-new-5-minute-alzheimers-test-and-then-do-this</guid>
      <link>http://www.caring.com/blogs/take-the-new-5-minute-alzheimers-test-and-then-do-this/comments</link>
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      <title>Comment on How to Care for Someone Who Has Cancer - AND a Negative Attitude</title>
      <description>
10:00 AM CST...Melanie, this blog is a little confusing; the &quot;comments&quot; read as though written by a child.

What type of cancer? How Long has he/she had it? Is the family not telling you anything ?

If the cancer is terminal your friend has the right to know. I would approach your friend's doctor and put the question(s) directly to him/her. If the doctor blinks too many times/stares at the floor/chews on his pencil or tells you &quot;talk to the family&quot; or avoids you in any way, I'd say your friend doesn't have much time in this Vale of Tears.
 
These are all reasonable adult-type questions. 
 
If they are your &quot;comments&quot; I sympathize with your pain, but you need to can the &quot;mantras&quot; and forget this line of &quot;discussion&quot; and spend as much &quot;quality&quot; time with your friend as possible.

He/she may appreciate that more than you depending on divine intervention or playing on the Blog machine.

Luck to you and your friend.   J.B.
</description>
      <author>James Ballard</author>
      <pubDate>Wed, 17 Jun 2009 15:24:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude</guid>
      <link>http://www.caring.com/blogs/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>I emailed this web page to my two siblings.  The results are in.  One emailed back and said thanks for the information.  That was a month ago.  Silence.  The other sibling sent an email with cuss words and a list with about 8 demands with what they WANTED.  I want    I want    I want. There was no &quot;What I can do&quot; list.  Again, I am an awful person etc.  There were 13 I's in there email. I did comply with some of the wants with an email in return. Finances, health, etc. and asked them to call at least once a week, and a visit every 2 months.(they do live in the same state).  They managed to be in this part of the state to shop.  Thank you for being here for me. Now I know why I had an imaginary friend when I was 4.      </description>
      <author>noexcuses</author>
      <pubDate>Wed, 17 Jun 2009 12:27:25 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on How to Care for Someone Who Has Cancer - AND a Negative Attitude</title>
      <description>nothing can help you cancer , but nothing can separate your presumed victims from the over powering love of the Supreme God.His love triumps over your cell destroying methods. we have your number,your sorry loser. </description>
      <author>Anonymous</author>
      <pubDate>Wed, 17 Jun 2009 03:55:36 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude</guid>
      <link>http://www.caring.com/blogs/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude/comments</link>
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      <title>Comment on How to Care for Someone Who Has Cancer - AND a Negative Attitude</title>
      <description>you , mr. cancer, are just like your name. you are a creep and we know your motive, but we will destroy your cells. </description>
      <author>Anonymous</author>
      <pubDate>Wed, 17 Jun 2009 03:52:26 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude</guid>
      <link>http://www.caring.com/blogs/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude/comments</link>
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      <title>Comment on How to Care for Someone Who Has Cancer - AND a Negative Attitude</title>
      <description>My sister inlaw will kill your efforts,mr.cancer. we together will whip your arse. </description>
      <author>Anonymous</author>
      <pubDate>Wed, 17 Jun 2009 03:50:46 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude</guid>
      <link>http://www.caring.com/blogs/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude/comments</link>
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      <title>Comment on How to Care for Someone Who Has Cancer - AND a Negative Attitude</title>
      <description>you are not welcome here. you are just a vagabon.</description>
      <author>Anonymous</author>
      <pubDate>Wed, 17 Jun 2009 03:49:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude</guid>
      <link>http://www.caring.com/blogs/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude/comments</link>
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      <title>Comment on How to Care for Someone Who Has Cancer - AND a Negative Attitude</title>
      <description>Cancer is such a theif. but we can win against it. it has no conscience but we do. so screw you mr.cancer you are a loser. we know your thieving ways and we can defend ourselves against you.you are a loser and we are winners.</description>
      <author>Anonymous</author>
      <pubDate>Wed, 17 Jun 2009 03:47:55 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude</guid>
      <link>http://www.caring.com/blogs/how-to-care-for-someone-whos-got-cancer-and-a-negative-attitude/comments</link>
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      <title>Comment on Take the New 5-Minute Alzheimer's &quot;Test&quot; &#8211;- And Then Do This</title>
      <description>I'm confused !  I took the test and added up my score....but there were no ranges of values to compare to, to see what the score means !

Did I miss something ?  I also tried to go to this website, which was mentioned, but nothing displays: http://www.tymtest.com/</description>
      <author></author>
      <pubDate>Tue, 16 Jun 2009 16:24:54 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/take-the-new-5-minute-alzheimers-test-and-then-do-this</guid>
      <link>http://www.caring.com/blogs/take-the-new-5-minute-alzheimers-test-and-then-do-this/comments</link>
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      <title>Comment on The #1 Reason You're So Tired (It's Not What You Think)</title>
      <description>I got diagnosed with apnea but I fit this description EXACTLY. Somehow I need to rid myself of the clogged ( restricted ) feeling and then all should be well. Maybe Steven N. knows the answer. Bandaids aren't perfect but they sometimes help until the fix comes around. Newborns seldom have the problerms of 67 year olds. They haven't had sufficient time to damage themselves. Names aside, it ain't fun to not sleep well and drag around all day !</description>
      <author></author>
      <pubDate>Tue, 16 Jun 2009 05:04:25 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/why-older-women-cant-sleep-a-new-explanation</guid>
      <link>http://www.caring.com/blogs/why-older-women-cant-sleep-a-new-explanation/comments</link>
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      <title>Comment on The #1 Reason You're So Tired (It's Not What You Think)</title>
      <description>Stated a few things I wasn't aware of and a few I knew.</description>
      <author>retiredgranny</author>
      <pubDate>Tue, 16 Jun 2009 04:38:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/why-older-women-cant-sleep-a-new-explanation</guid>
      <link>http://www.caring.com/blogs/why-older-women-cant-sleep-a-new-explanation/comments</link>
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      <title>Comment on The #1 Reason You're So Tired (It's Not What You Think)</title>
      <description>Sadly, we think an external cure will cure our internal disruptions.  No, changing how we think won't change how we feel, either.  Just ask a new born, who, like the rest of us is born sentient, but without the neurological &quot;wiring&quot; for cognitive reasoning. (Still, via our adult capacities for deduction, reflecting upon our culture of narcissism may be worthwhile.)
It seems we Americans suffer from maladies somewhat unique to the rest of the world(?), thus leading us into deeper dependency upon external sources to address symptoms, yet in the process avoid non-mechanistic, root causes.
That said, if you want to support the economy and buy the &quot;band- aids,&quot; well, maybe the resulting good-nights sleep will be nourishing enough to encourage one to go beyond the symptom based remedy.
Love Always,
Steven N.</description>
      <author>Steven N.</author>
      <pubDate>Mon, 15 Jun 2009 21:06:47 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/why-older-women-cant-sleep-a-new-explanation</guid>
      <link>http://www.caring.com/blogs/why-older-women-cant-sleep-a-new-explanation/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>WHAT DOES ANYONE THINK ABOUT THIS EMAIL EXCHANGE BETWEEN MY NIECE &amp; MYSELF TODAY?

FROM MY NIECE:  first i would like to say hello and hope you faimly is well. i wanted to do a quick note to inform you that hunters bday is at the end of the month. tomorrow i am haveing a major operation and will be off my feet for a long time. howveru i have faimly coming in as well and we are haveing a small party for hunter on the 28th and a bigger party july 11th. she is invited to both and i spoke to dad about and him and kathy will pick her up and drop her off on both days..


i did want to say also that i take great offense for you writeing and assumeing that we do not take grandmas happiness into consderation. It is very sad that you feel that way. Because it isn't true. Don't forget that we do have little ones and as a mother you know your self how busy it can be. Esp when my son has been ill and is also haveing surgery. Brooke mom and I always take grandma out and bring our kids to see her. Just because we don't do it when you want doesn't mean we ingore her or her feelings. Even if it is a couple days after her bday or holiday we still go and see her. Brooke and I both agree that we want our kids to spend as much time with her as possible and Morgan and Hunter love grandma and love seeing her. I'm sorry that our timings don't meet up with yours and I don't ever what to see anything in emails nor in the web page that makes it sound that she never gets to see her great grand kids, or that we ingore her or her feelings again. I am sure you will want to answer this email and I am very sad i didn't get this one sooner but I will be at my sisters and will not have a computer. Feel free to send me a letter through the mail if you wish

MY RESPONSE:

Re: What would make your Grandmother happy

Feeling a little guilty, are you?

You cannot dispute these facts:
1) Your Grandmother's 80th birthday was 3 months ago.
2) Nobody in the family even bothered to try to bring us all together for HER day.
3) Seeing her ENTIRE family all together would make your Grandmother happy.
4) Your Grandmother greatly enjoys the babies and visiting whenever anyone can do so.
5) I have never questioned or ridiculed such visits - I have merely pointed out that her ENTIRE family is not together.
6) I am part of her family, as are my husband and our daughter, yet we are not invited to family events - like your son's birthday and baby/bridal showers and weddings.

Your email makes it clear that no invitation to Hunter's party will be forthcoming to me or my family. I have absolutely no problem with that, especially considering I've never been allowed to meet him. That is YOUR choice for YOUR son. That is about YOU.

CarePages is not about you - it's about what I am doing for my Mother (your Grandmother) and trying to let the family know what's happening with her.

Here's another fact: I have asked, pleaded and begged my sister, brother and you to meet with me and a counselor (a person who has a neutral point of view) to resolve our differences so that we could work together as a team (team: two or more people who join together to achieve a common goal), the goal being to take care of my Mother (your Grandmother). My attempts have been ignored, questioned and ridiculed.

Now, with so many years having passed and nobody else in the family making any move to reconcile, I have let go of that ideal. I have accepted this and have found a new serenity in my life because I am no longer vainly hoping the rest of you will put aside your issues with me for HER benefit (your Grandmother). My new goal is to balance caring for my Mother (your Grandmother) with the needs of my husband and daughter - and maybe taking care of myself a little bit.

Oh, and please, don't pretend that I have any knowledge of the health or welfare of you, my sister, my brother or your families. I don't. I'm excluded by the rest of you, and you know it. Your excuses are not necessary and not good enough to validate your claim that you're considering what will make my Mother happy (your Grandmother).

There's only one way you can prove me wrong: Stop making excuses and accusations and get the entire immediate family (you, Rose, Andy, &amp; ME) together with a counselor (or an Arbitrator) to resolve our differences and work together at Grandma's house.

. . .

. . .

. . .

Don't worry: I'm not expecting you to take me up on it. You will no longer see any hopeful mention from me that we do something all together for my Mother (your Grandmother). That's up to the rest of you now. I'll be available.

My prayers always include all of you and I hope you all continue to include my Mother (your Grandmother) in your events.

It seems to me that with the way things have been, I guess the next time we'll all be together will be at your Grandmother's funeral.

Is THAT what you think she wants?

Love &amp; prayers,

Aunt Linda

</description>
      <author>sttng</author>
      <pubDate>Mon, 15 Jun 2009 01:29:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>noexcuses has hit the nail on the head.  Being the only caregiver with three siblings who are 'negative caregivers' nearly put me over the edge.  How great that you mentioned the isolation of the caregiver.  No matter how hard I try, there is nothing in my power to be done to make up for just ONE visit from either of the other three.  What few phone calls she receives revolve around their 'crisis'.  I never dreamed I could feel this way and you have made this day a good one for me.  You have put into words that which I could not.  Thank you!</description>
      <author>Anonymous</author>
      <pubDate>Sat, 13 Jun 2009 23:50:27 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on The #1 Reason You're So Tired (It's Not What You Think)</title>
      <description>Another reason I'm so tired is that my Mom, who has Dementia, is getting her days and nights mixed up. Last night she was up and moving every 1-2 hrs. This in turn wakes me up. I took her to daycare and then collapsed back into bed for 2 hrs of *uninterrupted* sleep!!!!! Betty J</description>
      <author>Anonymous</author>
      <pubDate>Fri, 12 Jun 2009 17:38:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/why-older-women-cant-sleep-a-new-explanation</guid>
      <link>http://www.caring.com/blogs/why-older-women-cant-sleep-a-new-explanation/comments</link>
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      <title>Comment on Reconciling With Siblings After a Fight Over Caregiving for a Parent</title>
      <description>You might add to your list of common reasons for sibling dispute over caregiving.  The reason I think there is such bad feelings is the isolation the caregiver experiences because the other siblings don't participate in visiting the elder parent or calling. The caregiving sibling becomes the enemy.  Excuses excuses excuses.  Wayne Dyer just came out with a new book about that subject.  Excuses become a bad habit and create havoc to all those that surround you.  I no longer waste my time with people who can't, over and over again.  Wayne Dyer says in his book that people that live making excuses for why they can't, don't have a healthy mind. The purpose is to figure out how you can.  For example.  Look at the calendar and mark times that as a sibling, a visit to the parent could be planned.  Call every Sunday evening on a regular basis. My daughter emails a letter to her Grandma to me and I print it out and deliver it to my Mom.  Photos are a very good way to keep in contact.  But silence, Very Cruel to my thinking.  In my family it is too late for any reconciliation and I have come to terms with that.  I have new siblings (cousins) and they deserve respect and appreciation for their family support and I celebrate that. I've tried to find the good in this situation of being the only caregiver for my Mom.  I don't think I would want to have my siblings lives.  I don't think I could do that to anybody, especially my Mother, as crazy as she is with alzheimers. I want to have some dignity and I want that for my Mom too.        </description>
      <author>noexcuses</author>
      <pubDate>Thu, 11 Jun 2009 13:29:40 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-conflict-over-caregiving</guid>
      <link>http://www.caring.com/blogs/sibling-conflict-over-caregiving/comments</link>
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      <title>Comment on 7 Health Conditions That Look and Sound Like Alzheimer's But Aren't Alzheimer's</title>
      <description>mom's 83 and having problems with memory,appitite,sleep,balance,diabetes,depression,etc.  couldn't be drinking like a rock star every day has anything to  do with it!  </description>
      <author>robert michael faul</author>
      <pubDate>Thu, 11 Jun 2009 07:20:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/7-health-conditions-that-look-like-sound-like-alzheimers-but-arent-alzheimers</guid>
      <link>http://www.caring.com/blogs/7-health-conditions-that-look-like-sound-like-alzheimers-but-arent-alzheimers/comments</link>
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      <title>Comment on Should There Be a Mandatory Driving Test for People 75 and Up?</title>
      <description>&quot;Should there be a mandatory driving test for people 75 and up?&quot;

Yes. And not just once: I think everyone should have to take a driving test periodically starting at 75. I know some people will say it's ageism, but by that logic, so are &quot;graduated&quot; licenses (used by many states to ensure safe driving habits among young people). The fact of the matter is, older drivers are more likely to get into fatal accidents than other adults. That's not discrimination, it's statistics.</description>
      <author>TheGrandChick</author>
      <pubDate>Thu, 11 Jun 2009 02:48:58 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/should-there-be-a-mandatory-driving-test-for-people-75-and-up</guid>
      <link>http://www.caring.com/blogs/should-there-be-a-mandatory-driving-test-for-people-75-and-up/comments</link>
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      <title>Comment on Wish Your Time Spent Caring for Older Family Members Could Be Paid? Maybe It Can</title>
      <description>I am in the position to be paid for my mother out of her funds right now, but can this be applied to her &quot;spending down of her assets&quot; when in a couple of years, she will have none and may qualify for Medical (California)?</description>
      <author>krod</author>
      <pubDate>Wed, 10 Jun 2009 21:36:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/wish-your-time-spent-caring-for-older-family-members-could-be-paid-maybe-it-can</guid>
      <link>http://www.caring.com/blogs/wish-your-time-spent-caring-for-older-family-members-could-be-paid-maybe-it-can/comments</link>
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      <title>Comment on Wish Your Time Spent Caring for Older Family Members Could Be Paid? Maybe It Can</title>
      <description>unfortunately I live in California where programs that pay family members for caring for family members is not available. If anyone out there knows of any that are available in California, please let me know by dropping me a line at bleueyez10@yahoo.com. It would be greatly appreciated.
</description>
      <author>bleueyez</author>
      <pubDate>Wed, 10 Jun 2009 18:05:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/wish-your-time-spent-caring-for-older-family-members-could-be-paid-maybe-it-can</guid>
      <link>http://www.caring.com/blogs/wish-your-time-spent-caring-for-older-family-members-could-be-paid-maybe-it-can/comments</link>
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      <title>Comment on How to Get Siblings to Help Pay for a Parent's Care</title>
      <description>When convening a family meeting to discuss distribution of responsibilities to care for a parent, a Geriatric Care Manager can be very helpful to provide objectivity, mediation, and insight into available resources.  If you are looking for a Care Manager, members of the National Association of Professional Geriatric Care Managers can be found by name and by zip code at www.caremanager.org.</description>
      <author>Betsy Evatt,  CMC</author>
      <pubDate>Wed, 10 Jun 2009 15:54:48 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-help-with-parent-care</guid>
      <link>http://www.caring.com/blogs/sibling-help-with-parent-care/comments</link>
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      <title>Comment on 5 Hot-Weather Bummers for Alzheimer's Caregivers</title>
      <description>Bathing is really a worrisome issue. We have a big comfortable tub, and my husband will sometimes consent to have a bath together when he has been refusing to shower. I try to keep the frequency down to still be able to offer it as something special when necessary. </description>
      <author>JeanetteNehls</author>
      <pubDate>Tue, 09 Jun 2009 17:56:26 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/5-hot-weather-bummers-for-alzheimers-caregivers</guid>
      <link>http://www.caring.com/blogs/5-hot-weather-bummers-for-alzheimers-caregivers/comments</link>
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      <title>Comment on The #1 Reason You're So Tired (It's Not What You Think)</title>
      <description>Gulf War vets and PWCs Persons With Chronic Illnesses have this problem, continuously. I have found that sleeping on my side, head elevated with minium of 2 pillows, plus pillow between my knees, work for all-time. If allergies, congestion, fungal overgrowth of the nasopharyngeal tract (nose, throat and esophogus) or viruses are a problem, a cool mist humidifier with distilled water and a small bottle of hydrogen peroxide do the job.
   I have been tested repeatedly for sleep apnea, to no avail. Chronic viruses related to military vaccines are the basic cause of my breathing and heart problems.</description>
      <author>beckiecann</author>
      <pubDate>Mon, 08 Jun 2009 17:58:48 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/why-older-women-cant-sleep-a-new-explanation</guid>
      <link>http://www.caring.com/blogs/why-older-women-cant-sleep-a-new-explanation/comments</link>
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      <title>Comment on How to Get Siblings to Help Pay for a Parent's Care</title>
      <description>We moved here almost 10 years ago to help my wifes mom take care of her sister. Her sister died almost 6 years ago and Mom quickly went downhill until now she care barely get out of bed to transfer to her potty chair. My wife suddenly became a 24/7 care provider for her mom while the rest of her family won't even visit because they know we will ask them to help out with mom. I have no relationship with my wife and I took a meaningless job just so I would be close in case Mom fell or ...worse. I hope I can find suggestions on getting through this but I'm not sure.</description>
      <author>Rev_Kerry</author>
      <pubDate>Sun, 07 Jun 2009 12:03:47 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-help-with-parent-care</guid>
      <link>http://www.caring.com/blogs/sibling-help-with-parent-care/comments</link>
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      <title>Comment on Push Our Buttons</title>
      <description>I dig it!  I have collected 161 Tips for Caregivers that I am putting into printed form right now.  It will be a wonderful place for me to blog.  Thank you. </description>
      <author>Joy Golliver</author>
      <pubDate>Fri, 05 Jun 2009 22:03:55 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/push-our-buttons</guid>
      <link>http://www.caring.com/blogs/push-our-buttons/comments</link>
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      <title>Comment on How to Get Siblings to Help Pay for a Parent's Care</title>
      <description>oops.  I mean &quot;these articles&quot;  are definitely useful.
My bad on grammar.</description>
      <author>Blue  Topaz</author>
      <pubDate>Fri, 05 Jun 2009 14:07:29 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-help-with-parent-care</guid>
      <link>http://www.caring.com/blogs/sibling-help-with-parent-care/comments</link>
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      <title>Comment on How to Get Siblings to Help Pay for a Parent's Care</title>
      <description>Thanks.  This are definitely useful.</description>
      <author>Blue  Topaz</author>
      <pubDate>Fri, 05 Jun 2009 14:06:44 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-help-with-parent-care</guid>
      <link>http://www.caring.com/blogs/sibling-help-with-parent-care/comments</link>
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      <title>Comment on How to Get Siblings to Help Pay for a Parent's Care</title>
      <description>All of the suggestions here can be discussed and implimented with the use of a FREE service offered on www.Lotsahelpinghands.com

You can create a free-of-charge, private, web-based community to organize family, friends, neighbors, and colleagues &#8211; a family&#8217;s &#8216;circles of community&#8217; &#8212; during times of need. 

This site makes it easy to coordinate activities and manage volunteers with their intuitive group calendar. Communicate and share information using announcements, messages boards, and photos too!

Using this type of 'service' makes everyone in your circle aware of &quot;what&quot; is needed and &quot;when&quot; and reduces the amount of followup required to make sure all events are covered. 

I am not affliated with this service, but I have created a website/center for my mother to eliminate misunderstandings, or 'dates' of events for our mother!</description>
      <author>Angel A</author>
      <pubDate>Wed, 03 Jun 2009 16:07:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sibling-help-with-parent-care</guid>
      <link>http://www.caring.com/blogs/sibling-help-with-parent-care/comments</link>
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      <title>Comment on 7 Health Conditions That Look and Sound Like Alzheimer's But Aren't Alzheimer's</title>
      <description>I wanted to share a similar situation. My husband was diagnosed at 65 with Alzheimer's. He had similar memory issues and had experienced some devastating issues with family that seemed to leave him in a total state of depression. When the &quot;depression&quot; did not subside I decided to have the doctor look at him and he was diagnosed with Alzheimer's. My husband went to &quot;the top neurologist&quot; in this metro area. During the five years under the care of his neurologist I noted on several doctor's appointments that I wanted to have another CT done of my husband's head since he appeared to not be regressing. The doctor repeated denied my request to have another CT done since I suspected NPH. Last October my husband was rapidly regressing in motor skills during a 2 week period. As it turned out, on my insistance, another emergency CT was done. The entire space between the brain and skull was filled with blood!! The fact the he even was alive was a miracle! Four holes were drilled into his skull to drain the 5 layers of OLD BLOOD! There has been some permanent damage to the brain but he is still alive and happy. Caregivers need to be acknowledged and doctors need to listen to what they are noticing in the patients!</description>
      <author></author>
      <pubDate>Wed, 03 Jun 2009 00:28:28 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/7-health-conditions-that-look-like-sound-like-alzheimers-but-arent-alzheimers</guid>
      <link>http://www.caring.com/blogs/7-health-conditions-that-look-like-sound-like-alzheimers-but-arent-alzheimers/comments</link>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>I was laughing when I read all this, sounds like a good description of me. I am over 40, 60 to be exact. I was caretaker for someone with altzheimers and yes, I wondered about me too....</description>
      <author>Anonymous</author>
      <pubDate>Tue, 02 Jun 2009 16:37:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on Bathing Blocks: When an Elder Refuses to Bathe</title>
      <description>Great article Kate,

I work on two elder care blogs and bathing is always a hot issue for us. 

A big danger issue that we see is shower doors. They are not strong enough to support the weight of an adult and are often relied upon dangerously. Check out the more here: http://www.rightathome.net/seniorhomecare/?p=155.

One of the best tips that we have seen work is to give the elder bathing the most power possible. Let them pick the bathing time and shampoo and soap. This seems to help them feel more comfortable.

If you are interested, check out more on our Senior Home Care Blog: http://www.rightathome.net/seniorhomecare.

Best,
Bill

</description>
      <author>RightatHome</author>
      <pubDate>Tue, 02 Jun 2009 15:16:00 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/elders-who-refuse-to-bathe</guid>
      <link>http://www.caring.com/blogs/elders-who-refuse-to-bathe/comments</link>
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      <title>Comment on 7 Health Conditions That Look and Sound Like Alzheimer's But Aren't Alzheimer's</title>
      <description>Wow I found info on LBD on fridAy last week. I am convinced thats what mom has,not AD. These Docs just throw more meds at you and they make alot of symptoms worse. If your loved one has Parkinsonian features AND Alzheimer symptoms check out The Lewy Body Dementia Association Website. </description>
      <author>mad127d@aol.com</author>
      <pubDate>Tue, 02 Jun 2009 13:08:36 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/7-health-conditions-that-look-like-sound-like-alzheimers-but-arent-alzheimers</guid>
      <link>http://www.caring.com/blogs/7-health-conditions-that-look-like-sound-like-alzheimers-but-arent-alzheimers/comments</link>
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      <title>Comment on 7 Health Conditions That Look and Sound Like Alzheimer's But Aren't Alzheimer's</title>
      <description>My mother was diagnosed with NPH 2 yrs ago. While she still has some vascular dementia, the shunt did help her to think a little clearer and helped with some of her incontence and walking. Fortunately we had a wonderful doctor who knew to refer her to a neurologist when I presented him with the ongoing symptoms.
Dawn - Columbus OH</description>
      <author>dawnsjns</author>
      <pubDate>Mon, 01 Jun 2009 12:34:28 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/7-health-conditions-that-look-like-sound-like-alzheimers-but-arent-alzheimers</guid>
      <link>http://www.caring.com/blogs/7-health-conditions-that-look-like-sound-like-alzheimers-but-arent-alzheimers/comments</link>
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      <title>Comment on Yummy Soft Foods For Seniors</title>
      <description>What a wonderful list of suggested resources. I've been caring for my brain injured 57 yr old husband for 2 yrs now. There are so many ordinary things that we take for granted, - like the ability to swallow food. Yet the process of moving the food through the mouth and down the throat without choking - is an incredibly complicated process. Just eating wears him out because every swallow is an effort requiring intense concentration. I'm definately going to check out the resources mentioned because I cook and prepare 95% of what he eats and I need new suggestions.</description>
      <author>cmacp</author>
      <pubDate>Sat, 30 May 2009 10:27:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/a-soft-food-diet-sure-doesnt-mean-bland</guid>
      <link>http://www.caring.com/blogs/a-soft-food-diet-sure-doesnt-mean-bland/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>Here's a riddle

What does an Alzheimer parent and an uncaring sibling have in common?

They both act childish and have lost their memory.

</description>
      <author>noexcuses</author>
      <pubDate>Fri, 29 May 2009 12:32:05 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>I realized that communication with my sisters is best through email, this was only after many phone conversation resulting in arguments just from the tone of their voices, never mind their ridiculous remarks.

My mom currently is living close to my home, in a senior residency and has a full time caretaker. I still have plenty of responsibility  but this has made it easier. I know she is in good hands. I get to see her several times a week &amp; she comes to my house, too.  I no longer need to ask them for anything!! When I did ask, you got it, I had some of the very same excuse you mentioned below.  Do you know them? :)</description>
      <author>noreen</author>
      <pubDate>Fri, 29 May 2009 01:47:27 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>Noreen....What I do is ask them to do things to help  my Mother by email.  I have documentation that way, plus excuses are different in writing.  They can be very creative, make you laugh or shiver in your boots. It does'nt matter what the reason is why you or your Mother may need support or help.  They will be busier, in worse health, (even more than your Mom) broke, afraid to drive, the stress of seeing her (because Mom pushes their triggers)oh yes, they don't want to run into you because you are controlling, were mean to them in 1st grade, took a vacation, etc. I'm sure you know how they stack up. 
These are my Mother's children, not mine.  My children call and visit her.    
 </description>
      <author>noexcuses</author>
      <pubDate>Thu, 28 May 2009 12:23:03 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>No need to clarify, I totally understood exactly what you meant. It is clear you want to protect your mom from any emotional hurt. I get it!

I know that my sisters would never be there for me.
Before this all happened I would have done anything for them.

I realize that my relationship with my sisters will never be. It took a few years to get to this point. Wishing, praying and hoping they would have an epiphany, but finally, I'm clear they won't ever get it.

Yes, there were many signs of selfishness through the years, but when my mom got sick it was clear there were no limits to their selfish ways. I had never really needed them and my mom never asked for help so when she got sick everything changed.  
 </description>
      <author>noreen</author>
      <pubDate>Thu, 28 May 2009 01:36:23 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>I need to claify the statement I look forward to when she will forget them.  A case manager once said &quot;If you have a deceased relative , and the alzheimer parent asks about them, don't put them through the pain of hearing about the loss, as if it were the first time.&quot;  I will be looking forward to when she no longer asks, because the realization is painful for her.</description>
      <author>noexcuses</author>
      <pubDate>Wed, 27 May 2009 13:24:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>Watching my Mom decline without their support and love is not easy.   That is what this really is all about.  I noticed you did not mention yourself not getting any love and support.  If this was not your Mother and you were in her place, would they be there for you?  Probably NOT.  Scary huh?  Rage, hurt,and anger do not feel good when you are trying to get through this part of your Mothers life and your own. I'm just glad I have the people at the ass't living taking the part as a family member.  They know, they see it all the time. It would be crazy making to have my Mother in my home.  She asks me the whole visit why my siblings don't come to see her or call. I'm looking forward to when she will forget them.  She no longer knows their childrens names, so I'm sure they will be next.  I try to talk about the family members , who are involved with her, and make it a positive conversation. You do know, I hope, that your relationship with your siblings will never be the same.  The family dysfuntion pops out during times like these.  I have one sibling that plays office politics with the family and the other thinks they are still the baby of the family and why am I not taking care of her perceived phobias.  If you really look back and even now,  how do your siblings handle life situations?  Do they get along with fellow employees, are they reliable in their job, or do you see a common theme?  So, don't take it personal, anybody would get this treatment, even during a time like this with a parent.  Have they left you stranded before?  Did you think this was a one time event?  Have you been left holding reservations or tickets, only to get a last minute cancellation from them? They like to keep their options open at all times.  Sprinkle a little white lie, bring in some drama, and poof &quot;Got out of that one.&quot;  There is always the possibility that it can  be about laziness. The reason you thought you needed a sanity check is because, you got a taste of their code of conduct.           </description>
      <author>noexcuses</author>
      <pubDate>Wed, 27 May 2009 12:29:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on 10 Tips for Better Sex After 50</title>
      <description>The trouble with oral sex,it can be treated as obligatory.and any one who dosn't agree to it,is inhibited,or frigid even abnormal. Dont be conditioned to accept all forms of sex by selfish  perverts,If you dont like it dont do it.</description>
      <author>octoman</author>
      <pubDate>Wed, 27 May 2009 08:11:31 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sex-after-50</guid>
      <link>http://www.caring.com/blogs/sex-after-50/comments</link>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>I think I saw here the question, &quot;What are the first signs of Alzheimer's disease?&quot; Since my mother was diagnosed with some form of dementia in 2002, I had to try to recall the first convincing symptoms of her dementia. Confusing the telephone for the TV remote control was one of the first signs that we picked up on. Leaving the phone &quot;off the hook&quot; repeatedly was another. Losing track of what day of the week it was seemed bizarre at the time, but now that I'm retired and have few outside demands on my time, I find myself failing to keep up with what day it is. I make all kinds of excuses for that! The fact that I don't feel compelled to get out for social interaction I excuse as just being lazy after having had to get dressed and out early for 37+ years to go to work. I read that social outlets are important, as well as physical activity being beneficial. I have to force myself to do both of those things.</description>
      <author>NeedGrace</author>
      <pubDate>Tue, 26 May 2009 23:01:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on 10 Tips for Better Sex After 50</title>
      <description>One thing missing from the piece was some encouraging talk about oral sex and &quot;69.&quot;
A &quot;cunning linguist&quot; can speak the language of love.</description>
      <author>Rob</author>
      <pubDate>Tue, 26 May 2009 16:59:08 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sex-after-50</guid>
      <link>http://www.caring.com/blogs/sex-after-50/comments</link>
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      <title>Comment on 10 Tips for Better Sex After 50</title>
      <description>I think sex can rule your life.Up till I was 77 years of age it ruled mine,then an operation on my wife went wrong and she had three prolapesd disks in her back and sex was too painful and she did not want to consider it.At first I was upset,my manhood had been deminished,but now after many months I find life without sex has its benefits.so dont be fooled into thinking life without sex is a deprived life.Before 77 years of age may be,now not at all.sex can be shared selfishness,me,me,me.but it also can be wonderful experience!but dont force it.     </description>
      <author>octoman</author>
      <pubDate>Tue, 26 May 2009 13:50:22 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/sex-after-50</guid>
      <link>http://www.caring.com/blogs/sex-after-50/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>IF I wasn't living it, it would be so difficult for me to believe that you were doing everything and then told you were the terrible person by your sibling. I actually thought I was losing my mind when I was being treated like I was the terrible one by my two siblings. I know that they will never ever get it. The way they deal with the guilt, &amp; shame is by denial and blame. I will never hear &quot;I'm sorry&quot; they could never look at themselves.    
I went to see a therapist for a sanity check. I asked &quot;how do you know it isn't me?&quot; The therapist said &quot;your mother made the decision to be with you, and you are the one that is doing it all.&quot; Clearly,
I still struggle with this disappointment from them. Watching my mom decline without their support and love is not easy.
 </description>
      <author>Anonymous</author>
      <pubDate>Tue, 26 May 2009 01:38:19 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>How did I let go of my spoiled siblings?  I listened to the silence.  
I could have asked,begged,pleaded for help because I broke my foot or the stress, even my health, but they would have bigger issues why they could not pick up any slack.
She was in independent living the first year.  I took care of her every day.  Changed her poopy sheets, cleaned her and her room.  At the end of the first year, I decided I need to think of me and my family. I moved her to ass't living.  I started talking to other women who's parent  lived in the same home and were the only caretaker in their family too.  I call them my Angels.  They guided me in how to get through this.  They had the same experience as me with their siblings.  I also read a book that was a great help &quot;Will I Ever be Good Enough.&quot; 
When I called my sibling to let her know I had moved Mom, she assumed I called to tell her she was in the hospital or dead. When she found out Mom had only moved, she did not ask about her health or how I was.  She told me what a terrible person I was.  I told her I would contact her when Mom was dead.          
To answer your question, how long before I faced reality?  1 year.  
Another good book &quot;Why is it Always about You?
I also have an Aunt, who this happened to and she is a shining example.  She is supportive and has no regrets.  She says it is better to give help and be able to live with yourself.
As far as hurt, yes it hurt and I cried, because I felt so alone.  But as you go through this life, people dissapoint you, even your own siblings.  That's why You have to take care of yourself.  Don't make them the center of attention with their bad behaviour.
good luck     </description>
      <author>noexcuses</author>
      <pubDate>Mon, 25 May 2009 16:27:53 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>When my mom got sick, I would have expected that my family would rally together. Instead my siblings heads went into the sand, (denial at it best) so I stepped up to the plate to take care of her-- and their rally was against me.
Accusations of being controlling. Sorry, I'm not going to sit back when mom's life is on the line. 
This is the time to act. CANCER!
The job of caretaker got harder (DEMENTIA) .... I was told this is that I wanted.
Are they narccisist? Do they lack the empathy gene? Are their memories so short that they don't remember all that mom did for them? How can they live with themselves?It is absolutely baffling to me. 
Anonymously posted ---Would you want these people in your life? Best to let them go!! I totally get it, but doesn't it hurt? How long did it take you to get to this point?


 </description>
      <author>Anonymous</author>
      <pubDate>Mon, 25 May 2009 03:19:57 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>My dad recently died from Shy-Drager syndrome, or Multiple Systems Atrophy, one of the Parkinsons-Plus disorders. I've privately wondered if these aren't variants of Alzheimer's, as I've read they involve the same tangling up of nerves in the brain. Also, James Doohan, the actor for Scotty on the original Star Trek, died of Alzheimer's and Parkinson's, and that also makes me wonder if the Parkinsons-plus disorders aren't variants of Alzheimer's. Robert</description>
      <author>Anonymous</author>
      <pubDate>Sun, 24 May 2009 04:05:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>My dad recently died from Shy-Drager syndrome, or Multiple Systems Atrophy, one of the Parkinsons-Plus disorders. I've privately wondered if these aren't variants of Alzheimer's, as I've read they involve the same tangling up of nerves in the brain. Also, James Doohan, the actor for Scotty on the original Star Trek, died of Alzheimer's and Parkinson's, and that also makes me wonder if the Parkinsons-plus disorders aren't variants of Alzheimer's. Robert</description>
      <author>Anonymous</author>
      <pubDate>Sun, 24 May 2009 04:04:46 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>It was a very good article.  The only thing that worries me is when I go to the bathroom and forget what I went in there for.  I'm 82 and still can joke about it all and a lot of other oldies can also, just read your article, I tell them.  Thanks for the article.  Ellen</description>
      <author>Anonymous</author>
      <pubDate>Sun, 24 May 2009 02:33:49 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>Great article (My God, I have it.  I forgot to spell article!) Seriously, my friends and I laugh a lot about such things as running upstair snd forgeting why and of course names, etc.  I am 78 almost 79 and pretty lucid.  Thanks. Gretchen</description>
      <author>Anonymous</author>
      <pubDate>Sun, 24 May 2009 02:06:04 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>Great article (My God, I have it.  I forgot to spell article!) Seriously, my friends and I laugh a lot about such things as running upstair snd forgeting why and of course names, etc.  I am 78 almost 79 and pretty lucid.  Thanks. Gretchen</description>
      <author>Anonymous</author>
      <pubDate>Sun, 24 May 2009 02:05:53 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>Interesting article.  I'm 65 &amp; facing similar symptoms.  Had some testing done. Dr. suggests not Alzheimers &amp; said that many other things can cause symptoms.  Some include impaired sleep, not enough exercise, hypertension, low B12 &amp; for males, low testosterone levels.  I can't remember the rest...</description>
      <author>Leland H.</author>
      <pubDate>Sun, 24 May 2009 01:28:21 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>I am not convinced. Although I have all these symptoms I still think I might have the weisenheimers or whatever you call that disease.</description>
      <author>Anonymous</author>
      <pubDate>Sat, 23 May 2009 22:46:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>Wonderful article! So clear and helpful. Thank you!</description>
      <author>Hank</author>
      <pubDate>Sat, 23 May 2009 20:37:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>Thank you - I think my family is more concerned than I am, so this is helpful for them.  I have trouble with nouns, sometimes, but I can describe what I'm talking about &amp; the word comes to me as I'm doing it.  I have no worries, especially after reading your info!</description>
      <author>Anonymous</author>
      <pubDate>Sat, 23 May 2009 20:32:27 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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      <title>Comment on Depression, Women, and Menopause -- a Hot Topic We Need to Talk About</title>
      <description>When my late wife was going through menopause in her late 30's the doctor prescribed birth control pills to suppliment her hormones. I don't advise doing that. By the time she was in her early 40's she was a wreck. She was constantly turning the termostat in the house up and down, and the poor gal was miserable all the time. She died at 46 due to a blood clot from a foot surgery that traveled to her fragile lungs. I miss her terribly. </description>
      <author>Anonymous</author>
      <pubDate>Fri, 22 May 2009 16:13:06 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/depression-women-and-menopause-a-hot-topic-we-need-to-talk-about</guid>
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      <title>Comment on Depression, Women, and Menopause -- a Hot Topic We Need to Talk About</title>
      <description>There is no question that depression, mood swings, sadness, anxiety, lack of sleep, aches and pains have all started affecting me at 50.   I have never been a 'depressed' type and exercise vigorously almost daily.  So its NOT 'in my head' and thanks to the individuals below I am making an appointment with a recommended FEMALE gynecologist of similar age and getting some form of treatment!!!</description>
      <author></author>
      <pubDate>Fri, 22 May 2009 15:22:19 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/depression-women-and-menopause-a-hot-topic-we-need-to-talk-about</guid>
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      <title>Comment on Depression, Women, and Menopause -- a Hot Topic We Need to Talk About</title>
      <description>When I was going through menopause (and peri-menopause), I became terribly anxious and my depression became much worse.  I have never felt right for the last 10 or so years, with each year getting progressively worse.  Not one OBGYN would help me, always indicating basically that it was no &quot;big deal.&quot;  I finally most recently went to an osteopathic family doctor who does hormone testing by saliva testing.  Sure enough my progesterone and DHEA were low.  I am now taking bio-identical hormones which I just started, and I am beginning to feel much less anxiety and depression.  

I believe that this is something that any woman suffering from a similar experience should definitely consider.  It's really going the alternative route as opposed to the traditional, standard route which has a totally different approach to the problems.</description>
      <author>Anonymous</author>
      <pubDate>Fri, 22 May 2009 14:40:47 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/depression-women-and-menopause-a-hot-topic-we-need-to-talk-about</guid>
      <link>http://www.caring.com/blogs/depression-women-and-menopause-a-hot-topic-we-need-to-talk-about/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>I truely understand my mother &amp; I was taking care of my great grand mother w/alzheimer's........mind now she hand 19 grands &amp; 32 greatgrands kids everyone had something to do.. So my mother took her to her house she would have her at night then my turned in the mornings  for about 4 months it were very hard because at the time my three kids were very young and she were fighting trying to get out tha house..but the scary thing were that she were forgetting us and I didn't understand what alzheimer's were.. But at the end the Dr. and attorney adviced my mother to put her in a long care facility..that made me get in tha medical feild cause I wer very angry at my family members when she have took care of our mothers &amp; fathers and help took care of my cousin &amp; myself..I didn't understand how could they jus forget and turn their back on her when she needed them the most..she died in my mother arms 10/30/02 she were 92 years old...The nursing homes is full of residents jus like my grandmother sum family members forget about them...</description>
      <author>mseve</author>
      <pubDate>Fri, 22 May 2009 04:30:27 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
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      <title>Comment on Dementia Alert: The Scary Complication Nobody Tells You About</title>
      <description> Donna
I just went through this with my mom when she had hip surgery. She, too, went completely &quot;out of her head&quot;; I was totally unprepared for it; nobody had every said anything to me about something like this possibly happening. The only possible inkling would be that her nurse practitioner had told me she seemed forgetful at her first office visit which is why she asked her to have me call them and let them know when I could come before they would schedule her surgery. (she lives out-of-state) but forgetful is one thing, physical is another which is what she was in the hospital. She has always been somewhat verbal toward me (and I'm an only child) but much less so toward my adult son so I actually called him in with the idea she would be calmer with him. That did possibly help somewhat but he was there in the daytime while I was there at night when she was more confused. I did manage to leave while he was there during the day and talked to a neighbor who was a nurse who told me about &quot;sundowner's&quot; being somewhat common after hip surgery - again no one had ever mentioned this. My father-in-law had this with his COPD but I never related that to this. It means what is says; she was more confused as the sun went down; she would think she was at a dear friend's house. I never thought to try to have anything in her room, but I did call this friend and told her; she then played along with her. Mom was upset about being at this friend's house and imposing on her, taking her bed; she kept trying to get up out of the hospital bed to leave to go home; this friend first tried to help her understand where she was but that only upset her more but when she took the tact that it was okay for her to be at her house even telling her what room she was in, that it wasn't her own; that seemed to calm her, at least for the moment but it didn't last. At bedtime the nurse put an alarm on her that at first I thought was hooked up to the nurses system such that it would alert them so I could get some rest. I found out otherwise when it went off and woke me up finding her out of the bed trying to go the bathroom (the actual room in her room).She at this point did not have a bedside chair because she wasn't supposed to be using one yet; she wasn't supposed to even be getting out of her bed without a nurse. I still at this point thought a nurse had been alerted and would be coming to help. She was trying to hurt me for not letting her go by herself,which is what a passing nurse heard (she probably would have seen the whole situation had the door been left open but a previous nurse had closed it for quiet at bedtime)and reported me for being abusive for. She wasn't supposed to be restrained. She probably should have been given some more medication but she didn't have any ordered. My understanding is the doctor's office was more concerned about medicine reactions and long-term effects than her actions. (I suppose in her case this was a valid concern since she had trouble even coming out of the anesthetic from surgery in times past without giving her any more medicine to depress her system) Maybe I shouldn't get this specific but she was trying to pull out her catheter which wasn't supposed to come until the next day; finally a nurse realized it would be better to go ahead and take it out rather than let her hurt herself; she was trying to go herself which is why it was agitating her so and was able to do so when she took it out.   The nurses, however, just shrugged it off , not as dementia or anything like that because she didn't have that documented on her chart but just her medicine. However, at the time I was very frightened, stressed and confused. She was being given her own medicine so that didn't make sense to me but one of those meds was an anti-depressant she was on that I suppose in one sense should have helped; except that I suppose in this situation she was actually the opposite of depressed plus she didn't normally take it the way it was prescribed so in actuality she was being given more of it than she normally took so I felt in some ways that may have actually contributed to the problem. She also had a &quot;nerve pill&quot; med in her room that she wasn't being given. She was, instead, being given that out of hospital supply that wasn't the exact same thing as hers. It may have been supposed to have been but hers was generic and the hospital is required to give brand name; she was taking Lorazepam and they were giving her Atavan. It may have been supposed to help calm her down but she seemed to have a reaction to it that made her worse. She at least was agitated over it not looking like her own meds. I have since learned that at least in these situations you can ask the doctor to permit the patient to take all their own meds which are not directly related to their reason for hospitalization. I now believe the doctor was correct; I learned from the home health care nurse after mom came home that the medicine they were talking about at the hospital was what they used for her spinal they gave her for her hip surgery, which she said normally is morphine; then I understood. I do agree now, however, with the doctor. Even though the nurse said the morphine typically takes longer to pass through an older person's system (just because their system is slower just like all the rest) it still was only a matter of weeks not months before she was back to &quot;normal&quot; and herself. She said that is why hydration is so important as well as elimination. She also said that is a real problem with the nurses at the hospital.</description>
      <author>Anonymous</author>
      <pubDate>Fri, 22 May 2009 01:14:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-alert-the-scary-complication-nobody-tells-you-about</guid>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>There must be something psychological that happens to the siblings that won't help with the care of an elderly alzheimer parent.  Both of my siblings decided they were mad at me and no longer talked to me.  I guess that means my demented Mother gets the same treatment.  Either they bury their head in the sand or they are true narcissists (lack of empathy).  I guess the shocking part is the realization that they don't care for me or their Mother.  I grieved.  But now, I feel liberated.  They are NO LONGER in my life and NEVER will be again.  I pretend I am an only child. I do what I can do for my Mother and have replaced my siblings with people who are supportive and mentally healthy.  I became friends with two of my Mothers nieces who adore her.  They email and ask about her and even visit her.  We have picnics and family gatherings and copy old family photos. My siblings snub has been a blessing in disquise. I made the best of a situation they were hoping would crush me.  Shame and guilt. I choose not to be in its web. These were the siblings my Mother took care of when they divorced etc. and had no where to go. She gave them cars looked after their child, paid for this and that. Would you want these people in your life? It's best to let go of them.

                          </description>
      <author>Anonymous</author>
      <pubDate>Thu, 21 May 2009 12:58:11 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
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      <title>Comment on A New Gel That Treats Esophageal Cancer: A Welcome Hope</title>
      <description>I have a tape of Nigella Lawson's late husband John Diamond's book C in which he discribes the treatment he received for esophageal cancer. a harrowing experience I couldn't blame him for contemplating suicide.I could not have even contemplated the treatment he undertook,I am lucky to be born a coward.</description>
      <author>octoman</author>
      <pubDate>Thu, 21 May 2009 09:53:04 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/esophageal-cancer-longshot-but-any-hope-is-welcome</guid>
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      <title>Comment on Depression, Women, and Menopause -- a Hot Topic We Need to Talk About</title>
      <description>I am about to turn 50 and have been getting waves of horrible depression like clockwork. It is very dark and deep but thankfully lasts only a few days - for now. Thanks for the heads up on this. I thought it was just me.</description>
      <author>Anonymous</author>
      <pubDate>Thu, 21 May 2009 03:11:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/depression-women-and-menopause-a-hot-topic-we-need-to-talk-about</guid>
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      <title>Comment on 12 Signs You Probably DON'T Have Alzheimer's</title>
      <description>I can't tell you how comforting that was!  For a moment I was afraid to take the test.  But then, I told myself that I had to take it and it was great!  Thank you, thank you, thank you!</description>
      <author>Anonymous</author>
      <pubDate>Wed, 20 May 2009 22:46:51 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/12-signs-you-probably-dont-have-alzheimers</guid>
      <link>http://www.caring.com/blogs/12-signs-you-probably-dont-have-alzheimers/comments</link>
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    <item>
      <title>Comment on A Surprising Gift Older Adults Often Need: Good Shoes (and How to Pick the Right Pair) </title>
      <description>I couldn't agree more- proper shoes always make a great gift, especially since 90% of Americans are wearing the wrong size shoe! And if women can't resist high heels, its best to stick with a low heel- you can often fit an orthotic in heels lower than 3 inches (which can be a lifesaver for the mom on the go!) And with recent technology, 'orthopedic' shoes are becoming more stylish than ever.  It's never too late to give your feet the attention they deserve ;)

..and don't forget, with fitness shoes, its always safe to go up a 1/2 size when you wear athletic socks.  It gives that extra 'wiggle room' that your toes desperately need!
</description>
      <author>KatieI</author>
      <pubDate>Wed, 20 May 2009 20:29:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair</guid>
      <link>http://www.caring.com/blogs/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair/comments</link>
    </item>
    <item>
      <title>Comment on A Surprising Gift Older Adults Often Need: Good Shoes (and How to Pick the Right Pair) </title>
      <description>I couldn't agree more- proper shoes always make a great gift, especially since 90% of Americans are wearing the wrong size shoe! And if women can't resist high heels, its best to stick with a low heel- you can often fit an orthotic in heels lower than 3 inches (which can be a lifesaver for the mom on the go!) And with recent technology, 'orthopedic' shoes are becoming more stylish than ever.  It's never too late to give your feet the attention they deserve ;)

..and don't forget, with fitness shoes, its always safe to go up a 1/2 size when you wear athletic socks.  It gives that extra 'wiggle room' that your toes desperately need!
</description>
      <author>KatieI</author>
      <pubDate>Wed, 20 May 2009 20:29:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair</guid>
      <link>http://www.caring.com/blogs/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair/comments</link>
    </item>
    <item>
      <title>Comment on A Surprising Gift Older Adults Often Need: Good Shoes (and How to Pick the Right Pair) </title>
      <description>I couldn't agree more- proper shoes always make a great gift, especially since 90% of Americans are wearing the wrong size shoe! And if women can't resist high heels, its best to stick with a low heel- you can often fit an orthotic in heels lower than 3 inches (which can be a lifesaver for the mom on the go!) And with recent technology, 'orthopedic' shoes are becoming more stylish than ever.  It's never too late to give your feet the attention they deserve ;)

..and don't forget, with fitness shoes, its always safe to go up a 1/2 size when you wear athletic socks.  It gives that extra 'wiggle room' that your toes desperately need!
</description>
      <author>KatieI</author>
      <pubDate>Wed, 20 May 2009 20:29:44 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair</guid>
      <link>http://www.caring.com/blogs/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair/comments</link>
    </item>
    <item>
      <title>Comment on A Surprising Gift Older Adults Often Need: Good Shoes (and How to Pick the Right Pair) </title>
      <description>I couldn't agree more- proper shoes always make a great gift, especially since 90% of Americans are wearing the wrong size shoe! And if women can't resist high heels, its best to stick with a low heel- you can often fit an orthotic in heels lower than 3 inches (which can be a lifesaver for the mom on the go!) And with recent technology, 'orthopedic' shoes are becoming more stylish than ever.  It's never too late to give your feet the attention they deserve ;)

..and don't forget, with fitness shoes, its always safe to go up a 1/2 size when you wear athletic socks.  It gives that extra 'wiggle room' that your toes desperately need!
</description>
      <author>KatieI</author>
      <pubDate>Wed, 20 May 2009 20:29:42 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair</guid>
      <link>http://www.caring.com/blogs/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair/comments</link>
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      <title>Comment on A Surprising Gift Older Adults Often Need: Good Shoes (and How to Pick the Right Pair) </title>
      <description>I couldn't agree more- proper shoes always make a great gift, especially since 90% of Americans are wearing the wrong size shoe! And if women can't resist high heels, its best to stick with a low heel- you can often fit an orthotic in heels lower than 3 inches (which can be a lifesaver for the mom on the go!) And with recent technology, 'orthopedic' shoes are becoming more stylish than ever.  It's never too late to give your feet the attention they deserve ;)

..and don't forget, with fitness shoes, its always safe to go up a 1/2 size when you wear athletic socks.  It gives that extra 'wiggle room' that your toes desperately need!
</description>
      <author>KatieI</author>
      <pubDate>Wed, 20 May 2009 20:29:31 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair</guid>
      <link>http://www.caring.com/blogs/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair/comments</link>
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      <title>Comment on Depression, Women, and Menopause -- a Hot Topic We Need to Talk About</title>
      <description>I have been in menopause for 12yrs.I'm 52, with a 82yr. old back,and need a hip replacement.I have a long time to go, and who would want to live like that??? And the golden years?? Forget it unless of course you have insurance.Not on a fixed income, not in this life...</description>
      <author>Anonymous</author>
      <pubDate>Wed, 20 May 2009 15:27:14 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/depression-women-and-menopause-a-hot-topic-we-need-to-talk-about</guid>
      <link>http://www.caring.com/blogs/depression-women-and-menopause-a-hot-topic-we-need-to-talk-about/comments</link>
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      <title>Comment on The In-Home Care Dilemma: Realizing You Need It, Figuring Out How to Afford It</title>
      <description>This article was very helpful.  Thank you.  I am in a similar situtation.</description>
      <author>Dianak2</author>
      <pubDate>Tue, 19 May 2009 21:02:44 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-in-home-care-dilemma-when-you-know-you-need-it-how-to-afford-it</guid>
      <link>http://www.caring.com/blogs/the-in-home-care-dilemma-when-you-know-you-need-it-how-to-afford-it/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>This should be the care givers bill of rights!</description>
      <author>wilibeme55</author>
      <pubDate>Tue, 19 May 2009 20:14:33 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>I will send this to my 5 brothers and sisters. I am power of attorney and nothing I do or say is right. They will not help me,I am stressed,tired and mad.
And they never like anybody I get to help out with keeping mom.Nit pick everything that goes on or is done to the house.
But I have and will not give up on my mom.She took care of me for 18 years,now I must take care of her for a few years,and no one knows how long they have.As I have always said,and believe, You are dieing from the day you are born, no one knows how long they have,so do the best you can, be cause
 it could be sooner than you think!
I pray that I can keep on doing for mom as long as she needs me to.But a break would be nice.
And as it seems I am not alone in this world,it seems a lot of us have the same problem!</description>
      <author>wilibeme55</author>
      <pubDate>Tue, 19 May 2009 20:11:34 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>OMG...this is so helpful. My younger brother just took my mom for a few days because my MOM needed a break from the older sister the caretaker. It is great but he did not take care of all the little important things and does not communicate at all with his other siblings nor does my mother. Do we let go and hope for the best or get verbally abused with his disrepectful attitude. There is no normal caring conversations discussed regarding the shared care of my mother and this is only hurting her. What to do if do not have any family support system?</description>
      <author></author>
      <pubDate>Tue, 19 May 2009 18:43:54 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on The In-Home Care Dilemma: Realizing You Need It, Figuring Out How to Afford It</title>
      <description>this article is a rehash of every take care of mom article I have ever read.  &quot;stay tuned&quot; for how to pay for it?????  Time to be real - get to the heart of the matter and leave the heroic daughters making casseroles stories for another blog.</description>
      <author>Snickersmom</author>
      <pubDate>Tue, 19 May 2009 17:56:30 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-in-home-care-dilemma-when-you-know-you-need-it-how-to-afford-it</guid>
      <link>http://www.caring.com/blogs/the-in-home-care-dilemma-when-you-know-you-need-it-how-to-afford-it/comments</link>
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      <title>Comment on The In-Home Care Dilemma: Realizing You Need It, Figuring Out How to Afford It</title>
      <description>this article is a rehash of every take care of mom article I have ever read.  &quot;stay tuned&quot; for how to pay for it?????  Time to be real - get to the heart of the matter and leave the heroic daughters making casseroles stories for another blog.</description>
      <author>Snickersmom</author>
      <pubDate>Tue, 19 May 2009 17:56:29 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-in-home-care-dilemma-when-you-know-you-need-it-how-to-afford-it</guid>
      <link>http://www.caring.com/blogs/the-in-home-care-dilemma-when-you-know-you-need-it-how-to-afford-it/comments</link>
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      <title>Comment on The In-Home Care Dilemma: Realizing You Need It, Figuring Out How to Afford It</title>
      <description>Great article, and thanks for pointing out the differences between hiring an independent caregiver vs. one from an agency.

Agencies are great, but are also expensive. www.Caresquare.com is a good alternative to agencies, as it equips families directly with the ability to run their own background checks and check references themselves right on the site. Hope this helps!</description>
      <author>arielkford</author>
      <pubDate>Tue, 19 May 2009 17:53:25 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-in-home-care-dilemma-when-you-know-you-need-it-how-to-afford-it</guid>
      <link>http://www.caring.com/blogs/the-in-home-care-dilemma-when-you-know-you-need-it-how-to-afford-it/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>PS:  This article should be published to a broader audience.
Perhaps a large newspaper, or Oprah Winfrey's magazine etc?

Or better yet ask to be on her show?
YEA!!</description>
      <author>Anonymous</author>
      <pubDate>Tue, 19 May 2009 16:31:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>That was awesome! That article should be available to every single caregiver.

I am not a caregiver now, but if I were I would sent this anonymously to my family, friends and relatives.
As a matter of fact, I think I shall do that anyway.

Hats off the the author!</description>
      <author>Anonymous</author>
      <pubDate>Tue, 19 May 2009 16:28:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>The dirty duz are right on. Additionally, I think a letter to ALL friends and relatives (special version to siblings, children, etc.)TELLING THEM what's going on with Mom or Dad, telling them what you need and how they can help, when to visit and how to conduct themselves on a visit. This is where you find out who really cares. But make it a NICE letter!  </description>
      <author>Rob</author>
      <pubDate>Tue, 19 May 2009 16:17:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on For Those Who Want to Age In Place, Lots of New Choices</title>
      <description>Great post Nell,

Yeah, it really seems like the Aging in Place movement is really gainings steam. Beyond granny flats and special home additions for seniors it seems like there is a big rise in in-home care. I work on an in-home blog and I see more and more stories on it everyday. 

If you are interested, check out our blog at http://www.rightathome.net/seniorhomecare.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 19 May 2009 15:43:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/many-new-aging-in-place-choices</guid>
      <link>http://www.caring.com/blogs/many-new-aging-in-place-choices/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>Sad but true, this society still expects the daughter to shoulder most of the responsibility of taking care of the elderly parent, AND the husband, AND the kids, AND a job, AND manage the finances AND the cooking, cleaning, shopping, etc. It's TOO MUCH.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 19 May 2009 15:10:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on 5 Real Sources of Hope About Alzheimer's Disease</title>
      <description>I felt that the parts of the Alzheimer's project I was able to watch was good,factual and well done.  I think it is every seniors worse nightmare and every caregivers fear!!!  I have always said the kindest thing about AD is the loved one forgets they have it.  </description>
      <author>Anonymous</author>
      <pubDate>Tue, 19 May 2009 14:01:36 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/5-real-sources-of-hope-about-alzheimers-disease</guid>
      <link>http://www.caring.com/blogs/5-real-sources-of-hope-about-alzheimers-disease/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>vjimw - I spent 7 years agonizing over how to MAKE them help. Needless to say, that didn't work. The depression and emotional drain over the pain they caused our Mom was affecting my health &amp; my personality. Now I'm enjoying everyday life &amp; focusing on positive things I can do to balance my time &amp; energy on HEALTHY thoughts.</description>
      <author>sttng</author>
      <pubDate>Sat, 16 May 2009 19:41:25 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>Noreen - you're NOT alone.  The more I talk with people, the more I learn that far too many familes don't pull together.  You will be the one with the clear conscience.  The suggestions in this article may work for some people. If they do - great! If they don't, you'll know you tried. The 2 most important things I've learned that have kept me sane: 1) forgiveness &amp; reconciliation are not the same thing and 2) they don't have to answer to me - but they will have to answer to God.  The most helpful thing I've done was change my goal, which had been for us to work together as a team to help Mom.  That's a faulty goal because its success depends on the actions of other people.  My &quot;breakthrough&quot; came when I finally set my sights on another idea:  to manage my mother&#8217;s care and strive to balance her needs with taking care of my husband and daughter . . . and maybe even taking care of myself a little bit.  Taking care of yourself is a NECESSITY - not a luxury.</description>
      <author>sttng</author>
      <pubDate>Sat, 16 May 2009 19:32:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on The In-Home Care Dilemma: Realizing You Need It, Figuring Out How to Afford It</title>
      <description>Terrific article.  Thanks for the real-life insight into your decision process.  </description>
      <author>MattJohnson</author>
      <pubDate>Fri, 15 May 2009 22:08:54 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-in-home-care-dilemma-when-you-know-you-need-it-how-to-afford-it</guid>
      <link>http://www.caring.com/blogs/the-in-home-care-dilemma-when-you-know-you-need-it-how-to-afford-it/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>sttng - That sounds like an amazing book.  I wish I had not spent so long agonizing about my siblings' lack or help (and awareness of the problem) and just concentrated my energy on taking care of my parents, myself and my relationship with my partner.</description>
      <author>vjimw</author>
      <pubDate>Fri, 15 May 2009 01:03:17 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>Great article with good suggestions. My mother in law is in failing health and of her 3 children only my spouse is caretaking for her. One sibling is 3,000 miles away and offers help but never follows through. The other sibling is 30 minutes away but works 50 hours a week and only helps sporadically. Thank you for the ideas.</description>
      <author>Bianca</author>
      <pubDate>Thu, 14 May 2009 14:37:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>I would like to help with the book!! I too feel like am an only child with two sisters significantly older than me, who I spent years loving and respecting. 
They do so little to help my mom they are so busy with their own lives. They turned it all around made me the bad one. Not only did they get mad at me they destroyed my relationship with their kids.--- I've lost both my two sisters( and their families) at a time when I needed them the most. IT is so difficult watching my mom decline ALONE IT has been awful -so tremendously painful, like a bad dream!
I am so angry, which I know isn't good for me.
The anger is not because they did this to me but 
because they did this to mymom --her whole life has been about family she doesn't deserve this.</description>
      <author>noreen</author>
      <pubDate>Thu, 14 May 2009 14:20:42 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>There are so many great ideas embedded in these comments, the power of group-think! Thanks for sharing them -- </description>
      <author>Paula Spencer</author>
      <pubDate>Wed, 13 May 2009 22:13:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
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      <title>Comment on A Surprising Gift Older Adults Often Need: Good Shoes (and How to Pick the Right Pair) </title>
      <description>Lots of Skechers have velcro and come in cute styles. I got my mom some for Christmas. She has arthritis so laces are doable, but time-consuming. She liked the Skechers so much, we went back and got another pair a few weeks later, and I think she just recently got another pair while out shopping with Dad. And no, I don't work for the company!</description>
      <author>Zella</author>
      <pubDate>Wed, 13 May 2009 16:10:35 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair</guid>
      <link>http://www.caring.com/blogs/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair/comments</link>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>I know what you mean.  My sister &amp; brother are 8 &amp; 7 years older than me, so much of my childhood was like I was an only child.  Now I'm taking care of Mom as if I were - my siblings don't bother to talk to me or ask about her, so I just do what I think is best for Mom.

My siblings (and their children) have caused so much pain. They exclude me from ALL family functions - weddings, baby showers, birthdays and holidays. Mom was so upset when I wasn't invited to that first baby &amp; bridal shower (two different nieces - one from each sibling), she said she wasn't going to go. I talked with her for about an hour to calm her down &amp; finally convinced her to go. I even took Mom shopping for a gift to give the bride (it wasn't from me) and the gift was REFUSED.

It's so hard to believe, and impossible to understand, how they can ignore my requests to help Mom and not care how much she is hurt. I know there will come a time when Mom won't remember these things or know who any of us are. At least then they won't be able to hurt her any more.</description>
      <author>sttng</author>
      <pubDate>Wed, 13 May 2009 10:36:49 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
    </item>
    <item>
      <title>Comment on When Mother's Day Means Grief, Not Joy</title>
      <description>Thanks everyone for your lovely comments. It means a lot to hear that my story has resonance for others.</description>
      <author>Melanie Haiken</author>
      <pubDate>Wed, 13 May 2009 03:04:18 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/when-mothers-day-means-grief-not-joy</guid>
      <link>http://www.caring.com/blogs/when-mothers-day-means-grief-not-joy/comments</link>
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    <item>
      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>Wow! I grew up like an only child.  Now I wish I was one. I knew I would have the responsibility of caring for my parents.  And I knew that my family would offer limited or no help.  But still I was not prepared for the emotional hurt not only to me but to my parents.</description>
      <author>Wezie</author>
      <pubDate>Wed, 13 May 2009 02:21:05 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
    </item>
    <item>
      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>As I take care of my elderly parents I have been telling my friends that I am glad I am an only child because I don't have those exact 12 issues stated above to deal with.</description>
      <author>Mendy</author>
      <pubDate>Wed, 13 May 2009 02:04:14 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
    </item>
    <item>
      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>This sounds like I could of written it. I commend you that you are finding time to write about the issues of family/siblings. One I wish to add is.. We told you what to do with Mother, and you choose to ignore it. Deal with it!</description>
      <author>Rendezvous 747</author>
      <pubDate>Tue, 12 May 2009 23:56:02 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dementia Alert: The Scary Complication Nobody Tells You About</title>
      <description>A light came on when I read the info on delirium versus dementia.  My mom had been experiencing a slight bit on confusion, and I had concerns she had a UTI.  She was successfully living alone and acutely became more confused.  She ended up in the hospital for 4 days (with a UTI and most like a touch of sepsis), and then to a nursing home for skilled therapy.  She is still there, and her dementia is much worse.  I am now convinced it is delirium, as she fits many of the symptoms. Is there any medication that may help with this issue?  I plan to take this info with me next week to her care plan &amp; medicare meetings to try to get her skilled benefits extended.   </description>
      <author>susan99504</author>
      <pubDate>Tue, 12 May 2009 22:27:04 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-alert-the-scary-complication-nobody-tells-you-about</guid>
      <link>http://www.caring.com/blogs/dementia-alert-the-scary-complication-nobody-tells-you-about/comments</link>
    </item>
    <item>
      <title>Comment on When Mother's Day Means Grief, Not Joy</title>
      <description>Thank you for telling your story.  Not enough is written when it comes to the very troubled relationships some of us have with parents. So many painful feelings when parents become elderly because the rage is there and yet we have to show respect and compassion for them in this stage of their life.  How to reconcile all of this, I do not know.  Thanks again for sharing your pain.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 12 May 2009 22:19:52 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/when-mothers-day-means-grief-not-joy</guid>
      <link>http://www.caring.com/blogs/when-mothers-day-means-grief-not-joy/comments</link>
    </item>
    <item>
      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>If anyone is interested, I'm writing a book about the stress &amp; heartbreak when siblings/family won't help. I was having medical problems because of how stressed I was from trying to MAKE them understand and help.  

This article gives suggestions for siblings about HOW to help.  My book will be about learning how to accept the fact that they won't.  It begins with the diagnosis, denial, excuses, broken promises, family meetings, ignored proposals, counseling, begging for help, more broken promises, anger, prayer, pain - heartbreaking pain, more counseling (for myself this time), prayer, forgiveness and acceptance.  It's been a long journey for me, and our mother's only in the early stages of Alzheimer's. 

If anyone's interested, let me know.  </description>
      <author>sttng</author>
      <pubDate>Tue, 12 May 2009 20:29:05 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
    </item>
    <item>
      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>Whew, I just clicked on this site out of morbid curiousity since only the first line of the page title showed and said &quot;The Junk Wars: 8 ways to get rid of aging parents&quot;

Guess you only need to push the comment button one time, eh?</description>
      <author>Anonymous</author>
      <pubDate>Tue, 12 May 2009 20:26:30 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
    </item>
    <item>
      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>In some circumstances, a good way to unburden everyone emotionally attached to, or burdened by, excess property, is choosing to sell at auction.  (In fact, a probate court may order an auction if a will is lacking, debts are owed, or due to embattled or neglectful heirs).  With an auction nothing is thrown away and unwanted property is converted to cash.  Its easy to sell small lots at a consignment auction house, many even offer pick-up service.  If you have a large amount of property, an on-site auction can avoid the cost and work of moving, and the auctioneers crews will do all of the work. Call each auctioneers listed in your area, then meet with least three, discuss all costs for ads, set-up, workers, commissions etc, and get an estimate in writing, ask for references and call them. Read the contract before signing. Auctions can also avoid or resolve battles between heirs for cherished items and the competitive bidding puts the money back into the estate.  Expect to pay 10 to 40% of the sale value for auction services. 

If you have the fortitude, time and energy and need to maximize cash return you can combine a family reunion with a garage sale or estate sale.  You can tag you items or take offers.  If you haggle hard and promote your event well, you can sum out ahead of an auctions proceeds by doing it yourself, but you may still have a pile of leftovers for the recycling center and local charities.  If your parents are going to help, make them promise not to give anything away once the item has been designated for the sale, not even to the grandkids.   

Ebay is another alternative for a few items, especially valuable collectibles.  On line auctions involve a lot of work unless you contract someone to sell and ship the items.

Be assured that for each and every discarded item there was a lamenting collector who would have gladly parted with good money to save that treasure from the ride to the landfill or the flames of the burn barrel.   </description>
      <author>Anonymous</author>
      <pubDate>Tue, 12 May 2009 20:22:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
    </item>
    <item>
      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>In some circumstances, a good way to unburden everyone emotionally attached to, or burdened by, excess property, is choosing to sell at auction.  (In fact, a probate court may order an auction if a will is lacking, debts are owed, or due to embattled or neglectful heirs).  With an auction nothing is thrown away and unwanted property is converted to cash.  Its easy to sell small lots at a consignment auction house, many even offer pick-up service.  If you have a large amount of property, an on-site auction can avoid the cost and work of moving, and the auctioneers crews will do all of the work. Call each auctioneers listed in your area, then meet with least three, discuss all costs for ads, set-up, workers, commissions etc, and get an estimate in writing, ask for references and call them. Read the contract before signing. Auctions can also avoid or resolve battles between heirs for cherished items and the competitive bidding puts the money back into the estate.  Expect to pay 10 to 40% of the sale value for auction services. 

If you have the fortitude, time and energy and need to maximize cash return you can combine a family reunion with a garage sale or estate sale.  You can tag you items or take offers.  If you haggle hard and promote your event well, you can sum out ahead of an auctions proceeds by doing it yourself, but you may still have a pile of leftovers for the recycling center and local charities.  If your parents are going to help, make them promise not to give anything away once the item has been designated for the sale, not even to the grandkids.   

Ebay is another alternative for a few items, especially valuable collectibles.  On line auctions involve a lot of work unless you contract someone to sell and ship the items.

Be assured that for each and every discarded item there was a lamenting collector who would have gladly parted with good money to save that treasure from the ride to the landfill or the flames of the burn barrel.   </description>
      <author>Anonymous</author>
      <pubDate>Tue, 12 May 2009 20:21:30 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
    </item>
    <item>
      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>In some circumstances, a good way to unburden everyone emotionally attached to, or burdened by, excess property, is choosing to sell at auction.  (In fact, a probate court may order an auction if a will is lacking, debts are owed, or due to embattled or neglectful heirs).  With an auction nothing is thrown away and unwanted property is converted to cash.  Its easy to sell small lots at a consignment auction house, many even offer pick-up service.  If you have a large amount of property, an on-site auction can avoid the cost and work of moving, and the auctioneers crews will do all of the work. Call each auctioneers listed in your area, then meet with least three, discuss all costs for ads, set-up, workers, commissions etc, and get an estimate in writing, ask for references and call them. Read the contract before signing. Auctions can also avoid or resolve battles between heirs for cherished items and the competitive bidding puts the money back into the estate.  Expect to pay 10 to 40% of the sale value for auction services. 

If you have the fortitude, time and energy and need to maximize cash return you can combine a family reunion with a garage sale or estate sale.  You can tag you items or take offers.  If you haggle hard and promote your event well, you can sum out ahead of an auctions proceeds by doing it yourself, but you may still have a pile of leftovers for the recycling center and local charities.  If your parents are going to help, make them promise not to give anything away once the item has been designated for the sale, not even to the grandkids.   

Ebay is another alternative for a few items, especially valuable collectibles.  On line auctions involve a lot of work unless you contract someone to sell and ship the items.

Be assured that for each and every discarded item there was a lamenting collector who would have gladly parted with good money to save that treasure from the ride to the landfill or the flames of the burn barrel.   </description>
      <author>Anonymous</author>
      <pubDate>Tue, 12 May 2009 20:21:29 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
    </item>
    <item>
      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>In some circumstances, a good way to unburden everyone emotionally attached to, or burdened by, excess property, is choosing to sell at auction.  (In fact, a probate court may order an auction if a will is lacking, debts are owed, or due to embattled or neglectful heirs).  With an auction nothing is thrown away and unwanted property is converted to cash.  Its easy to sell small lots at a consignment auction house, many even offer pick-up service.  If you have a large amount of property, an on-site auction can avoid the cost and work of moving, and the auctioneers crews will do all of the work. Call each auctioneers listed in your area, then meet with least three, discuss all costs for ads, set-up, workers, commissions etc, and get an estimate in writing, ask for references and call them. Read the contract before signing. Auctions can also avoid or resolve battles between heirs for cherished items and the competitive bidding puts the money back into the estate.  Expect to pay 10 to 40% of the sale value for auction services. 

If you have the fortitude, time and energy and need to maximize cash return you can combine a family reunion with a garage sale or estate sale.  You can tag you items or take offers.  If you haggle hard and promote your event well, you can sum out ahead of an auctions proceeds by doing it yourself, but you may still have a pile of leftovers for the recycling center and local charities.  If your parents are going to help, make them promise not to give anything away once the item has been designated for the sale, not even to the grandkids.   

Ebay is another alternative for a few items, especially valuable collectibles.  On line auctions involve a lot of work unless you contract someone to sell and ship the items.

Be assured that for each and every discarded item there was a lamenting collector who would have gladly parted with good money to save that treasure from the ride to the landfill or the flames of the burn barrel.   </description>
      <author>Anonymous</author>
      <pubDate>Tue, 12 May 2009 20:21:15 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
    </item>
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      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>Amen, amen, amen!  These are 12 seemingly small things that have HUGE impact to those of us who are caregivers.  It's great that you put this together to validate the feelings we often have.  Thanks!</description>
      <author>8 is enough!</author>
      <pubDate>Tue, 12 May 2009 17:38:01 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
    </item>
    <item>
      <title>Comment on Dirty Dozen: 12 Ways Hands-on Caregivers Are Driven Crazy by Their Siblings</title>
      <description>Amen, amen, amen!  These are 12 seemingly small things that have HUGE impact to those of us who are caregivers.  It's great that you put this together to validate the feelings we often have.  Thanks!</description>
      <author>8 is enough!</author>
      <pubDate>Tue, 12 May 2009 17:37:58 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings</guid>
      <link>http://www.caring.com/blogs/dirty-dozen-12-ways-hands-on-caregivers-are-driven-crazy-by-their-siblings/comments</link>
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      <title>Comment on Dementia Alert: The Scary Complication Nobody Tells You About</title>
      <description>Dealing with delerium has become something the patient care person MUST be concerned about.

In working with my wife (Stage IV colon cancer) only the strongest meds relieve her pain, so when Xanax was added to the mix of Methadone and Dialaudid during Chemo days, I knew to expect something.

As it turns out, because I was there, she was comfortable admitting she was having halucinations and I helped her relax through them. As good as the nursing is, I know no nurse has the time to hold a patients hand and reassure them for four to five hours.

Needless to say, we are not using the Xanax now except in extreme situations, and then only if someone is with her.

Kudos to all you loving caregivers out there. You really make a difference!</description>
      <author>Gabriel</author>
      <pubDate>Tue, 12 May 2009 16:52:10 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-alert-the-scary-complication-nobody-tells-you-about</guid>
      <link>http://www.caring.com/blogs/dementia-alert-the-scary-complication-nobody-tells-you-about/comments</link>
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    <item>
      <title>Comment on When Mother's Day Means Grief, Not Joy</title>
      <description>Thank you for giving an eloquent, authentic voice to something so complicated and overwhelming.  And I hope you had a fabulous Mother's Day with your daughters.  </description>
      <author></author>
      <pubDate>Tue, 12 May 2009 16:21:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/when-mothers-day-means-grief-not-joy</guid>
      <link>http://www.caring.com/blogs/when-mothers-day-means-grief-not-joy/comments</link>
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      <title>Comment on Dementia Alert: The Scary Complication Nobody Tells You About</title>
      <description>I have discovered various causes for mother's periods of delerium over the past few years.  Perhaps this list will be helpful to others:
extreme pain meds such as oxycontin and morphine, the Exelon memory patch (!), urinary tract infections (the first major symptom for her is the beginning of delerium - agitation, negativity), dehydration and other variations of electrolyte imbalance (especially low potassium), even severe constipation.  We were suspicious of several other meds (the statins and xanax, for example) because of the medical literature indicating problems and took her off those prophylactically.  It is difficult to get MD's to take the delerium seriously as a medical conition, but since the delerium goes away when the medical problem is solved or the drug is stopped, I now always look for something physical that causes these periods of delerium.  Mother consistentlt returns to her normal level of dementia and personality as soon as the physical problem is resolved.</description>
      <author></author>
      <pubDate>Tue, 12 May 2009 16:19:40 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-alert-the-scary-complication-nobody-tells-you-about</guid>
      <link>http://www.caring.com/blogs/dementia-alert-the-scary-complication-nobody-tells-you-about/comments</link>
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      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>Went I die I would like everything I own to disappear, like in O'Henry's poem &quot;One Hoss Shay&quot; where everything falls apart into molecules and atoms and the wind blows it away. But I would add to that, whereever my name appears on any registry, military records, social security, bank accounts, and etc. to also vanish into thin air and definitely no grave or any marker that I was alive.
</description>
      <author>Only 67</author>
      <pubDate>Tue, 12 May 2009 15:51:53 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
    </item>
    <item>
      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>I found a great book that helps you deal with Dealing With Your Parents Lifetime Accumulation Of Stuff it's called The Boomer Burden.  It was written by a real Estate Lady. Great book, it was helpful when we needed!!! She is a really great person to be able to help so many others deal with this difficult topic.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 12 May 2009 15:10:58 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
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      <title>Comment on Dementia Alert: The Scary Complication Nobody Tells You About</title>
      <description>Yes, we found out about this delirium thing the hard way. My mother went completely out of her head in the hospital and rehab. facility after breaking her hip. Her dementia had accelerated to the point she was physically violent, verbally abusive, confused and demanding to talk to relatives who had passed on years ago. The Drs. and nurses just shrugged it off as her alzheimer's and gave her Valium on top of her Xanax to keep her from hurting herself as well as the staff. It was a frightening, stressful, and confusing time for all of us. 8 months later she seems back to her &quot;normal&quot; stage of dementia and has calmed down somewhat. This is a serious problem that will only get worse as baby boomers age. More research, information and education is needed for medical personnel and caregivers to deal with this mentally, physically and financially draining situation of dementia and delirium.</description>
      <author>doforanimals</author>
      <pubDate>Tue, 12 May 2009 14:52:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-alert-the-scary-complication-nobody-tells-you-about</guid>
      <link>http://www.caring.com/blogs/dementia-alert-the-scary-complication-nobody-tells-you-about/comments</link>
    </item>
    <item>
      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>This advice is wonderful, and not just for helping the elderly. I'm an archivist, and helping my mother clean out my grandmother's house after we moved grandma to a nursing home was...trying. Mom wanted to keep all the supposedly-valuable collectibles and toss all the &quot;family papers&quot;, while I was focused on the unique family memories. The idea of taking photos of bulky items is great. I also use this idea for favorite items of my daughters' (clothing, toys) so that it is easier on me to pass these items onto the next owner rather than keeping them for sentimental reasons.</description>
      <author>Anonymous</author>
      <pubDate>Tue, 12 May 2009 14:09:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
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      <title>Comment on &quot;But Dad, You Just Ate&quot;: How Alzheimer's Changes Appetite and What to Do About It</title>
      <description>I was so encouraged when I read that your dad eats and eats-my dad lost my mom 9 months ago suddenly-he has dementia/alzhimers/altered mental status- he has gained 40 lbs in 9 months- he neds to lose instead of gaining, keeps gaining, he falls all the time, never breaks anything and sometimes does not know who I am- the only child-or who his grandchildren are- I have to work andmy usband works night shift-so I stay at home in the morning til my husband comes home-so we are with dad most of the time-dad can hardly walk, he has sat in a chair for 9 months and done nothing, tried physcial therapy- he will nto do the excersies, he just wants to be with mom-which is out of his hands- I need a support group so I can hear things like I did, that some of these patients eat and some don't-dad does liket  drink gin, and that does not help any of the issues, but he keeps saying you have taken everything away from me, please don't take the gin-
I hope that someone will read my short story- (sorry it is so long) and help me with just a e mail of support-

thank you
Bonnie Lassiter
bglassiter1@bellsouth.net</description>
      <author></author>
      <pubDate>Tue, 12 May 2009 13:49:11 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/changing-eating-habits-from-alzheimers</guid>
      <link>http://www.caring.com/blogs/changing-eating-habits-from-alzheimers/comments</link>
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      <title>Comment on A Surprising Gift Older Adults Often Need: Good Shoes (and How to Pick the Right Pair) </title>
      <description>where can you find velcro shoes anymore?</description>
      <author>momwacko</author>
      <pubDate>Tue, 12 May 2009 13:44:07 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair</guid>
      <link>http://www.caring.com/blogs/the-gift-older-adults-usually-need-good-shoes-and-how-to-pick-a-smart-safe-pair/comments</link>
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      <title>Comment on Breaking Through Isolation: Is it Fatigue, Depression, or Loneliness?</title>
      <description>More good facts and symptoms on depression in the elderly at http://www.seniorcare-stl.com/index.php/did-you-know-depression-in-seniors/ </description>
      <author>kevinh</author>
      <pubDate>Tue, 12 May 2009 13:43:41 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/is-it-loneliness-exhaustion-depression-or-all-three</guid>
      <link>http://www.caring.com/blogs/is-it-loneliness-exhaustion-depression-or-all-three/comments</link>
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      <title>Comment on When Mother's Day Means Grief, Not Joy</title>
      <description>Very brave, Melanie, and moving. I'm sure many others can relate to how you feel. I, too, hope your day with the girls was all you wished for.</description>
      <author>Sarah Henry</author>
      <pubDate>Tue, 12 May 2009 03:34:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/when-mothers-day-means-grief-not-joy</guid>
      <link>http://www.caring.com/blogs/when-mothers-day-means-grief-not-joy/comments</link>
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      <title>Comment on When Mother's Day Means Grief, Not Joy</title>
      <description>Probably the most moving Mother's Day piece I've ever read. I hope your day with your daughters was good both for you and for them.</description>
      <author>Anonymous</author>
      <pubDate>Mon, 11 May 2009 05:48:23 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/when-mothers-day-means-grief-not-joy</guid>
      <link>http://www.caring.com/blogs/when-mothers-day-means-grief-not-joy/comments</link>
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      <title>Comment on Caregivers' Fear of the Inevitable</title>
      <description>may be the good thing for caregiver is make the same thing that can be made from the real heart, love and care, everythings is nice to be ....</description>
      <author>kritsana</author>
      <pubDate>Sat, 09 May 2009 09:38:47 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/caregivers-fear-of-the-inevitable</guid>
      <link>http://www.caring.com/blogs/caregivers-fear-of-the-inevitable/comments</link>
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      <title>Comment on When Mother's Day Means Grief, Not Joy</title>
      <description>Hi Melanie,

My mom died of the same thing and I'm pretty sure I know how you feel. This is my 3rd mother's day without having to buy some useless gift she won't even remember I gave her. It is a relief but not a celebration. I know you are doing a great job of being an awesome mother, so it's your turn to just be celebrated. Enjoy the day.</description>
      <author>cynthia greenberg</author>
      <pubDate>Sat, 09 May 2009 05:43:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/when-mothers-day-means-grief-not-joy</guid>
      <link>http://www.caring.com/blogs/when-mothers-day-means-grief-not-joy/comments</link>
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      <title>Comment on Weight Loss: Keeping a Food Diary Makes a Difference</title>
      <description>I use &lt;a href=&quot;http://www.weightlosssoftware.com&quot;&gt;food diary&lt;/a&gt; called Food 
And Exercise Diary.&amp;nbsp; It is not free.&amp;nbsp; But it is professional.&amp;nbsp; 
www.WeightLossSoftware.Com</description>
      <author>tguez</author>
      <pubDate>Fri, 08 May 2009 20:02:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/weight-loss-keeping-a-food-diary-does-make-a-difference</guid>
      <link>http://www.caring.com/blogs/weight-loss-keeping-a-food-diary-does-make-a-difference/comments</link>
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      <title>Comment on Your Parent's Pet: Friend or Foe?</title>
      <description>When my mother had trouble seeing her black scottie against the dark rug, she put a light colored tee-shirt on him.  He was much easier to see.  With respect to larger dogs, a Gentle Leader or Haltie head collar works very well to prevent sudden lunges pulling you off your feet.  On icy days, I put head collars on both of my laborador retrievers (72 lbs each) and that has saved me from many a fall.</description>
      <author>SPeticolas</author>
      <pubDate>Wed, 06 May 2009 16:49:10 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/aging-relative-have-a-pet-what-to-know</guid>
      <link>http://www.caring.com/blogs/aging-relative-have-a-pet-what-to-know/comments</link>
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      <title>Comment on Dementia Alert: The Scary Complication Nobody Tells You About</title>
      <description>i know sunnysouth nurses act like your bothering them when you ask questions or become concerned about your loved ones overall care or medical conditons this is in regards to nursing home care.</description>
      <author>helpless </author>
      <pubDate>Wed, 06 May 2009 13:19:56 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-alert-the-scary-complication-nobody-tells-you-about</guid>
      <link>http://www.caring.com/blogs/dementia-alert-the-scary-complication-nobody-tells-you-about/comments</link>
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      <title>Comment on 5 Bills You Can Lower With a Phone Call</title>
      <description>And when all else fails, write to the CEO. Seriously, almost every company has a department, often called the &quot;executive office,&quot; which handles escalated complaints. Letters to CEOs or other senior executives are automatically routed there. You'll be amazed at how important you suddenly are, and how flexible the company you complained to can be! -Beth</description>
      <author>Anonymous</author>
      <pubDate>Tue, 05 May 2009 21:22:31 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/lower-your-bills-in-5-minutes-or-less</guid>
      <link>http://www.caring.com/blogs/lower-your-bills-in-5-minutes-or-less/comments</link>
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      <title>Comment on &quot;But Dad, You Just Ate&quot;: How Alzheimer's Changes Appetite and What to Do About It</title>
      <description>I have extreme difficulty getting my mother to eat anything, except chocolate. She won't do the Ensure or milkshakes - some days are a bit better, but she seems disinterested in food. </description>
      <author>Anonymous</author>
      <pubDate>Tue, 05 May 2009 17:38:22 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/changing-eating-habits-from-alzheimers</guid>
      <link>http://www.caring.com/blogs/changing-eating-habits-from-alzheimers/comments</link>
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      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>This summer I will be packing up/downsizing my Mom's home of 55 years, a home single-handedly built by my Dad, her husband of 51 years, for an out-of-area move to be closer to me.  The idea of taking photos of their home is absolutely priceless!  I am going to take photos of every aspect of their home and beautiful yard, as well as the surrounding neighborhood and neighbors.  In addition I will add photos of special places we frequented as a family.  All will go into a photo album which will be on her coffee table when she arrives at her new apartment at assisted living.  I think initially it will help her feel her grief of what was and can no longer be, and hopeful that one day soon it will be a fond reflection for her of happy memories.</description>
      <author>1-2Ponder</author>
      <pubDate>Tue, 05 May 2009 14:57:42 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
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      <title>Comment on &quot;But Dad, You Just Ate&quot;: How Alzheimer's Changes Appetite and What to Do About It</title>
      <description>I've also noticed my dad only likes foods that are easy to eat.  Meats particularly are very difficult as he has lost many teeth.  Most afternoons I fix a milkshake with whole milk and an Instant Breakfast and then he has an Ensure Plus two times a day along with his meals.  That way, I know he's getting nutrition even though he may not eat much of his meals.  A health care worker told me once that they would put sweet 'n low or sugar on the elder person's food no matter what it was.  Seems they would eat anything if it was sweet.  I haven't tried it yet as the thought of sugar on spaghetti just doesn't sound too appetizing.  But I may soon. </description>
      <author></author>
      <pubDate>Tue, 05 May 2009 14:57:23 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/changing-eating-habits-from-alzheimers</guid>
      <link>http://www.caring.com/blogs/changing-eating-habits-from-alzheimers/comments</link>
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      <title>Comment on Swine Flu: 10  Things You Need to Know to Protect Seniors</title>
      <description>I remember the french flue panic this seems to be a repeat performanceto me,the number of people dying from pig flue in Mexico is small compared with the none pig flue,the Mexicans have shot themselves in the foot.the loss of all the holidaymakers the beaches are empty as are the hotels.headless chickens comes to mind.I hope I am right!I was the last time.the only time my wife and I had flue during the past 15 years,was when we both had the flue jab?Remember 1916 they keep saying. </description>
      <author>octoman</author>
      <pubDate>Tue, 05 May 2009 14:28:09 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/prevent-swine-flu</guid>
      <link>http://www.caring.com/blogs/prevent-swine-flu/comments</link>
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      <title>Comment on Unforgettable Mother's Day Gifts for a Mom Who Forgets</title>
      <description>Those are some good ideas and I'll add mine--it doesn't have to be chocolates and flowers. My Mom's getting a package of pastrami and all the fixings from Katz's!  She's been jonesing for that for some time now.

But I have to add: Mother's Day this year (2009) is May 10th.  I should know, it's also my birthday. Postal rates go up the next day, May 11th.</description>
      <author></author>
      <pubDate>Tue, 05 May 2009 14:17:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/unforgettable-mothers-day-gifts-for-a-mom-who-forgets</guid>
      <link>http://www.caring.com/blogs/unforgettable-mothers-day-gifts-for-a-mom-who-forgets/comments</link>
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      <title>Comment on Dementia Alert: The Scary Complication Nobody Tells You About</title>
      <description>I think that you have to be really careful if the older person has hearing or vision loss because being in a new setting with these problems could throw anyone for a loop.
My problem has been nurses that act irritated when a family member has to 'interpret' for them to the patient. I feel like telling them that they should count their lucky stars that there is a family member involved to make their job a little easier!</description>
      <author>sunnysouth</author>
      <pubDate>Tue, 05 May 2009 14:07:50 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/dementia-alert-the-scary-complication-nobody-tells-you-about</guid>
      <link>http://www.caring.com/blogs/dementia-alert-the-scary-complication-nobody-tells-you-about/comments</link>
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      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>That's a great idea about taking pictures and creating an album of the items. When my late husband went into a nursing home at 33, he thankfully helped me sort through a list of items. While the process was frustrating, at the end of the day, he knew the new owners (relatives, friends and non-profits) could use the stuff better than either of us could in the throws of a healthcare crisis.</description>
      <author>Stacy Jensen</author>
      <pubDate>Tue, 05 May 2009 13:12:44 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
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      <title>Comment on Anti-Cancer Superfoods: Do They Really Work?</title>
      <description>anti-cancer super foods?I think I missed my column some where.but I do also have untreated cancer and I do follow a strict superfood diet 'see my comment 14 days back. </description>
      <author>octoman</author>
      <pubDate>Sun, 03 May 2009 16:43:08 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/anti-cancer-foods</guid>
      <link>http://www.caring.com/blogs/anti-cancer-foods/comments</link>
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      <title>Comment on Anti-Cancer Superfoods: Do They Really Work?</title>
      <description>No comments?well my wife had medical treatment she is in a wheelchair now,but her sister has arthiritis now,she is going to follow the treatment I followed.It was recommended by a doctor,if nobodies interested I wont put details but will say how my sister in law fare's with the treatment. </description>
      <author>octoman</author>
      <pubDate>Sun, 03 May 2009 16:34:42 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/anti-cancer-foods</guid>
      <link>http://www.caring.com/blogs/anti-cancer-foods/comments</link>
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      <title>Comment on Fear Alzheimer's? Try the Talking Cure</title>
      <description>after undergoing carotid artery bypass in 2004, my husband remained with short term memory.  The doctor(s) that have treated and the one currently taking care of him say he has moderate dementia.  Still the other s say he has alzheimer's.  My husband was perfect before his surgery.  I maintain something went wrong during surgery causing him to now have short term memory.  He is being treated with meds for alzheimer patients.</description>
      <author>Anonymous</author>
      <pubDate>Sat, 02 May 2009 20:07:28 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/fear-alzheimers-try-the-talking-cure</guid>
      <link>http://www.caring.com/blogs/fear-alzheimers-try-the-talking-cure/comments</link>
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      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>Another suggestion would be:  learn about the options for disposal and recycling that are available in your area, and offer to help.  I am caregiver to one person, and informally help two others as part of their support system.  Giving usable things to charity, or putting it in a consignment shop is an easy fix compared to trying to throw things out in a somewhat responsible and &quot;green&quot; way.  I have to drive 35 miles to a large recycling center to get rid of such things as old metal cookware, etc.  And it's hard to know what to do with broken televisions and small appliances </description>
      <author>Sopher's Mom</author>
      <pubDate>Sat, 02 May 2009 12:57:47 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
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      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>I tried many of those same things. Dad passed away and Mom has dementia, She double checked anyone leaving the house. &quot;They better not take my treasures&quot;. I finally started calling it my mess and kept appologizing. Mom finally told me to quit saying sorry and just clean it up. Unfortunatly Mom also told everyone else it was my mess and he can do it himself.</description>
      <author>Junier</author>
      <pubDate>Sat, 02 May 2009 03:44:31 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
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      <title>Comment on &quot;But Dad, You Just Ate&quot;: How Alzheimer's Changes Appetite and What to Do About It</title>
      <description>Dad also doesn't always remember eating a meal. My question to anyone who can help, he has Alzheimer's &amp; also is Diabetic. Does the additional Sugar he got a way with also contribute to the forgetfullness? Cuz He's always hungry. tried different combinations of meds for both.</description>
      <author>plumkrazzy</author>
      <pubDate>Fri, 01 May 2009 06:50:32 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/changing-eating-habits-from-alzheimers</guid>
      <link>http://www.caring.com/blogs/changing-eating-habits-from-alzheimers/comments</link>
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      <title>Comment on The Junk Wars: 8 Ways to Get Rid of Aging Parents' &quot;Stuff&quot; (and Your Resentment Over Having to Deal With It)</title>
      <description>Thanks for your helpful and entertaining account of cleaning out. I need to get going..

I'm reminded of when I was cleaning out my Grandmother's things. I had sent my Grandfather out for the day.  (She'd passed away several months before).  I worked into the night, and slept in the spare room.  The next morning, Grandfather came out and looked particularly grizzled.  

I'm sorry Grandfather, this must be very hard for you.  &quot;Actually,&quot; he said &quot;I simply can't find a razor, comb or toothbrush in the entire house!&quot; </description>
      <author>Anonymous</author>
      <pubDate>Fri, 01 May 2009 00:02:12 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it</guid>
      <link>http://www.caring.com/blogs/8-ways-to-get-rid-of-aging-parents-stuff-and-your-resentment-over-having-to-deal-with-it/comments</link>
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      <title>Comment on Swine Flu: 10  Things You Need to Know to Protect Seniors</title>
      <description>Both my parents are in their late 70's and information on this flu is very helpful... at this time of life they don't really need to get Seriously ill</description>
      <author>ESuze Anderson</author>
      <pubDate>Thu, 30 Apr 2009 21:30:21 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/prevent-swine-flu</guid>
      <link>http://www.caring.com/blogs/prevent-swine-flu/comments</link>
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      <title>Comment on Kicked Off Hospice for Not Dying Soon Enough</title>
      <description>It's really nice to know government hospice includes home care, or dying at home. Thanks. </description>
      <author>Anonymous</author>
      <pubDate>Thu, 30 Apr 2009 17:56:40 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/kicked-off-hospice-for-not-dying-soon-enough</guid>
      <link>http://www.caring.com/blogs/kicked-off-hospice-for-not-dying-soon-enough/comments</link>
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      <title>Comment on Swine Flu: 10  Things You Need to Know to Protect Seniors</title>
      <description>very helpful even though we are already health contious we still need to be reminded .</description>
      <author></author>
      <pubDate>Thu, 30 Apr 2009 17:49:17 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/prevent-swine-flu</guid>
      <link>http://www.caring.com/blogs/prevent-swine-flu/comments</link>
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      <title>Comment on &quot;But Dad, You Just Ate&quot;: How Alzheimer's Changes Appetite and What to Do About It</title>
      <description>I've noticed that my mother prefers meals that she doesn't have to chew too much ie. soups,casseroles etc.  When she has too chew foods like meats etc. she quickly becomes disinterested and stops eating.  Smaller snacks throughout the day such as tuna fish or egg salad on a soft bun seems to be effective.  Also she likes pizza.</description>
      <author></author>
      <pubDate>Thu, 30 Apr 2009 00:10:30 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/changing-eating-habits-from-alzheimers</guid>
      <link>http://www.caring.com/blogs/changing-eating-habits-from-alzheimers/comments</link>
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      <title>Comment on Swine Flu: 10  Things You Need to Know to Protect Seniors</title>
      <description>this helped me so much not to fear this diese so much and how to protect my family i also know not to worry about face masks ect thank you</description>
      <author>cherryrain</author>
      <pubDate>Wed, 29 Apr 2009 14:37:46 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/prevent-swine-flu</guid>
      <link>http://www.caring.com/blogs/prevent-swine-flu/comments</link>
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      <title>Comment on Avoid the Posthospitalization Communication Breakdown</title>
      <description>I just went through this with my husband.  First the emergency room doctor, then admited to hospital and a new doctor, who had to pass to a second.  I had to stop a procedure until it was throughly claified for me.  Then release to another skilled nursing facility and assigned a new doctor.  Now moved to a memory support unit.  All in about 10 weeks.  I am still spinning trying to get back in charge of my husbands health.  This is the worst challenge I have gone through in the eight years of Alzheimer's.  And now they all decided that he has Lewy Body!  I finally called in a advocate team to help get me back on track and in control.  Believe me it is worth it and sometimes pallative care is paid by medicare.  </description>
      <author>Joy Golliver</author>
      <pubDate>Tue, 28 Apr 2009 15:37:54 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/avoid-the-post-hospitalization-communication-breakdown</guid>
      <link>http://www.caring.com/blogs/avoid-the-post-hospitalization-communication-breakdown/comments</link>
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      <title>Comment on When Someone With Dementia Says, &quot;I Want to Go Home&quot;</title>
      <description>Sometimes when we say we &quot;want to go home&quot; we're not even talking about an earthly home at all. Before my wife went into the ICU, where she's now on life support, we talked about it and, like in the movie &quot;The Notebook&quot; (&quot;Second-Hand Lion&quot; is another great one!), we hoped to go home together ... to that place that was home before we came to this earth.</description>
      <author>omegareport</author>
      <pubDate>Sun, 26 Apr 2009 04:48:01 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/i-want-to-go-home</guid>
      <link>http://www.caring.com/blogs/i-want-to-go-home/comments</link>
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      <title>Comment on Anti-Cancer Superfoods: Do They Really Work?</title>
      <description>I had rhumatoid arthiritis 30 years ogo and rejected medical attention,changed my diet no uric acid in my diet and recovered a relative accepted all they could provide gold injections,steroids etc he died a cripple six years ago,he believed the treatment caused is disability. </description>
      <author>octoman</author>
      <pubDate>Sat, 25 Apr 2009 16:51:05 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/anti-cancer-foods</guid>
      <link>http://www.caring.com/blogs/anti-cancer-foods/comments</link>
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      <title>Comment on Avoid the Posthospitalization Communication Breakdown</title>
      <description>Your article was informative and very truthful about the lack of continuity of care during post-hospitalization.  One recommendation is that all patients be referred to an accredited Home Health Care Agency at discharge.  Medicare will pay 100%.  A nurse goes into the home, does a full comprehensive assessment, reviews and educates on all medications.  Most importantly, the nurse collaborates and communicates with all treating MD's.  Patients can also benefit from Physical Therapy, Occupational Therapy, Speech Therapy, Home Health Aides and a Social Worker through the Home Care Company.  All services are completely covered by Medicare.  Both of my parents have received excellent care from Amedisys Home Health over the past few years. They have been a lifesaver for me as a caregiver.</description>
      <author>Anonymous</author>
      <pubDate>Sat, 25 Apr 2009 02:41:22 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/avoid-the-post-hospitalization-communication-breakdown</guid>
      <link>http://www.caring.com/blogs/avoid-the-post-hospitalization-communication-breakdown/comments</link>
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      <title>Comment on Avoid the Posthospitalization Communication Breakdown</title>
      <description>Excellent,wonderfully helpful.I did not know about the lack of access to your primary care doctor!</description>
      <author>jennpenn </author>
      <pubDate>Fri, 24 Apr 2009 21:21:13 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/avoid-the-post-hospitalization-communication-breakdown</guid>
      <link>http://www.caring.com/blogs/avoid-the-post-hospitalization-communication-breakdown/comments</link>
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      <title>Comment on Watching Dad Dodder: How Much to Help (to Prevent a Fall) and How Much to Leave Him Alone?</title>
      <description>Falls are bound to happen (unfortunately) in both the home and institutional setting. My mother is just beginning to deal with some mobility issues and it's amazing to me that she shuns her cane. She regrets the things she can't do, but resists using the cane or even getting a Handicapped parking sticker for her car. She needs it.</description>
      <author>Stacy Jensen</author>
      <pubDate>Tue, 21 Apr 2009 19:54:05 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone</guid>
      <link>http://www.caring.com/blogs/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone/comments</link>
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      <title>Comment on The Surprising Thing Caregivers Want Most From Long-Distance Relatives</title>
      <description>I have been a caregiver for almost 5 years to my 84 year old aunt with mid stages of Alzheimer's. I need help, not a good word. All the good words do not replace someone saying &quot;let me help or let me takeover for a few days&quot; I have yet to see any of this from my family. Their 2 cents of help, hinders me more than helps. </description>
      <author>Anonymous</author>
      <pubDate>Tue, 21 Apr 2009 19:21:38 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-surprising-thing-caregivers-want-most-from-long-distance-relatives</guid>
      <link>http://www.caring.com/blogs/the-surprising-thing-caregivers-want-most-from-long-distance-relatives/comments</link>
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      <title>Comment on The Surprising Thing Caregivers Want Most From Long-Distance Relatives</title>
      <description>Joyg -- I love that idea (including the transition to orient them) and how it works out to benefit everyone in your family. And the comment that &quot;everyone CAN but doesn't&quot; is a good distinction, thx!</description>
      <author>Paula Spencer</author>
      <pubDate>Tue, 21 Apr 2009 16:52:02 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-surprising-thing-caregivers-want-most-from-long-distance-relatives</guid>
      <link>http://www.caring.com/blogs/the-surprising-thing-caregivers-want-most-from-long-distance-relatives/comments</link>
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      <title>Comment on New Hope for Liver Cancer</title>
      <description>Hi, I am a mother of five.  My oldest son, Michael (now 28) was diagnosed with a rare form of cancer, Neurofibrosarcoma, on March 19th, 2008  I am praying for a cure for all cancer patients.  As of right now, my son continues to battle this aggressive cancer.  Could you please write something on this website in regards to his type of cancer?  Many thanks!

Patti~</description>
      <author>Anonymous</author>
      <pubDate>Tue, 21 Apr 2009 16:42:06 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/new-hope-for-liver-cancer</guid>
      <link>http://www.caring.com/blogs/new-hope-for-liver-cancer/comments</link>
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      <title>Comment on Watching Dad Dodder: How Much to Help (to Prevent a Fall) and How Much to Leave Him Alone?</title>
      <description>My husband moved into an assisted living home.  In 8 weeks he has fallen 7 times.  No broken bones, but cut himself badly twice.  They don't seem to watch him like I did.  I don't think he can learn to use a walker because of his dementia.  He is young, 74, strong, and loves to walk.  They want to keep him in a wheelchair with an alarm.  He hates that.  I just don't know what to do.  I cannot move him to another home because we live in a CCRC situation.</description>
      <author>Joy Golliver</author>
      <pubDate>Tue, 21 Apr 2009 15:22:47 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone</guid>
      <link>http://www.caring.com/blogs/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone/comments</link>
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      <title>Comment on The Surprising Thing Caregivers Want Most From Long-Distance Relatives</title>
      <description>Don't say &quot;sub when you can&quot;, everyone can, the problem is they don't!!</description>
      <author>Anonymous</author>
      <pubDate>Tue, 21 Apr 2009 15:11:52 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-surprising-thing-caregivers-want-most-from-long-distance-relatives</guid>
      <link>http://www.caring.com/blogs/the-surprising-thing-caregivers-want-most-from-long-distance-relatives/comments</link>
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      <title>Comment on The Surprising Thing Caregivers Want Most From Long-Distance Relatives</title>
      <description>A caregtiver needs to ASK for specific needs.  I asked my sons who live far away to take turns and visit once a month.  On the first day I orient them to the current routine.  On the second day I leave for the whole day!  Usually I sit in a beautiful hotel and read, write, and brouse the shops.  This was so successful that now when the boys come they make me check into a hotel!  Fabulous!  The gift for them as been quality time with their day.</description>
      <author>Joy Golliver</author>
      <pubDate>Tue, 21 Apr 2009 15:02:24 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-surprising-thing-caregivers-want-most-from-long-distance-relatives</guid>
      <link>http://www.caring.com/blogs/the-surprising-thing-caregivers-want-most-from-long-distance-relatives/comments</link>
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      <title>Comment on Watching Dad Dodder: How Much to Help (to Prevent a Fall) and How Much to Leave Him Alone?</title>
      <description>My father also resisted using a cane or a walker.  After breaking a couple of bones in his lumbar region he really had no choice.  Luckily for me he also like walking in the stores.  He liked the security of pushing a cart and was convinced it could feel the same pushing a walker.  We got him one of those with the wheels, seat and breaks.  He calls it his &quot;quad&quot;  He too loves to walk around the yard and with his &quot;quad&quot; I don't have to worry.  He has a basket for his things and can sit down if he gets tired or wants to stop to pick something up or just look around.  I know it would have been a challange to get him to walk with one of the conventional walkers but he sure loves his &quot;quad&quot;!  Sometimes on his more unstable days I still walk with him but on most days I can let him go explore the yard on his own while I veiw from a distance.  It is so much better for us both for me not to have to hover anymore.  Good Luck.</description>
      <author>papasgirl</author>
      <pubDate>Tue, 21 Apr 2009 14:01:56 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone</guid>
      <link>http://www.caring.com/blogs/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone/comments</link>
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      <title>Comment on The Surprising Thing Caregivers Want Most From Long-Distance Relatives</title>
      <description>My wifes sister is going to Australia to look after her  elderly other sister who has dementia,to give  her sisters caring son a break for a month.last week she had an ergent phone call from a disabled friend when she got there it was her old dog needed the vet,so off to she went to get treatment. </description>
      <author>octoman</author>
      <pubDate>Tue, 21 Apr 2009 13:50:59 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-surprising-thing-caregivers-want-most-from-long-distance-relatives</guid>
      <link>http://www.caring.com/blogs/the-surprising-thing-caregivers-want-most-from-long-distance-relatives/comments</link>
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      <title>Comment on Watching Dad Dodder: How Much to Help (to Prevent a Fall) and How Much to Leave Him Alone?</title>
      <description>There are many other areas in which you can help your father besides doing it all for him. I would recommend that you let him do for himself, no matter how slowly he moves. He is moving and that prevents a fall. It is a form of activity. There are also other exercise programs available to seniors, i.e. Sit and Be Fit, Matters of Balance, etc...   Next look at environmental changes you can make to make his home  safer. Lighting, check and /or place photo cell night light in walk paths and in rooms. Rearrange furniture patterns to allow a walker to more easily navigate a walk path. Please send me a note on what areas specifically concern you and I will be glad to help address them with you. Your father does not have to fall. And thank you for being proactive, not reactive. </description>
      <author></author>
      <pubDate>Tue, 21 Apr 2009 13:34:45 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone</guid>
      <link>http://www.caring.com/blogs/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone/comments</link>
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      <title>Comment on The Surprising Thing Caregivers Want Most From Long-Distance Relatives</title>
      <description>This is great. I'm suddenly the long-distance relative of an everyday caregiver, and I'm grateful to know the ways I can truly help, without banking on my relative to ask me.</description>
      <author>Anonymous</author>
      <pubDate>Mon, 20 Apr 2009 17:01:27 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-surprising-thing-caregivers-want-most-from-long-distance-relatives</guid>
      <link>http://www.caring.com/blogs/the-surprising-thing-caregivers-want-most-from-long-distance-relatives/comments</link>
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      <title>Comment on How Furry Toys, Animals, and Dolls Help People With Dementia</title>
      <description>Aha, with a gigantic grin! my Mom's an &quot;elderly person with dementia&quot; and i'm a nearly 67 yr old &quot;youngster&quot; with autism, which covers both Paro's bases! That being True, at last Mom and me were Granted the JOY of sharing all my cuddly critters, whom i've always loved to make 
&quot;appropriate noises&quot; with as i move them about. What over-the-top entertainment we supplied each other day after day with that assortment of zoo (as well as tamer) creatures! Sure do vouch for this kind(of) PLAY with comfy critters to while away the daze! (ps ~ anybody got another TRADING HAPPY TALES to add to my/our Al. Support Group thread? Come and share, making the load a bit lighter for us all to bear! Jesus and val, loving UP^on y'all!) </description>
      <author>gollyboy</author>
      <pubDate>Mon, 20 Apr 2009 14:28:43 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/how-furry-toys-animals-and-dolls-help-people-with-dementia</guid>
      <link>http://www.caring.com/blogs/how-furry-toys-animals-and-dolls-help-people-with-dementia/comments</link>
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      <title>Comment on Anti-Cancer Superfoods: Do They Really Work?</title>
      <description>I looked at my comment about Wendy Richards.I have watched the TV program of her last months of life,many times.She was a greatlady she died as she lived,a true brit,campared with herI am a wimp!None of my naby-pamby,dark chocolate and ginger for her.I admire her strength of character.</description>
      <author>octoman</author>
      <pubDate>Sun, 19 Apr 2009 11:13:31 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/anti-cancer-foods</guid>
      <link>http://www.caring.com/blogs/anti-cancer-foods/comments</link>
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      <title>Comment on Anti-Cancer Superfoods: Do They Really Work?</title>
      <description> I had a thought,we are all different,so,green tea,may work for one person,cannabis hemp for another.Wendy Richards believed in chemotherapy as did Jade,I did not,anything that harms the immune system ,cannot be right.I find the bible very profound,I see it as symbolic not literal truth,I mean Noah's Ark is nonsense but symbolicly it has meaning,the garden of Eden the same thing I can pray to a symbolic God,it may only be talking to myself but my subconcious mind loves it,I get great comfort from it even praying for other people benefits me your are not helpless when you can pray.I know to some people I am talking rubbish,but there is so much rubbish,my little bit will not be noticed.</description>
      <author>octoman</author>
      <pubDate>Sat, 18 Apr 2009 20:15:19 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/anti-cancer-foods</guid>
      <link>http://www.caring.com/blogs/anti-cancer-foods/comments</link>
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      <title>Comment on Watching Dad Dodder: How Much to Help (to Prevent a Fall) and How Much to Leave Him Alone?</title>
      <description>You raise a good point that depending on the person's health situation a walker is sometimes more strongly recommended certain individuals -- but those can be even harder to get someone to go along with. You're right too that a doctor's recommendation can also be taken more seriously!</description>
      <author>Paula Spencer</author>
      <pubDate>Fri, 17 Apr 2009 18:59:29 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone</guid>
      <link>http://www.caring.com/blogs/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone/comments</link>
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      <title>Comment on The Surprising Thing Caregivers Want Most From Long-Distance Relatives</title>
      <description>Acknowledgment doesn't replace the much needed support that a caregiver truly needs, but don't ever miss a chance to acknowledge a caregiver. So what is acknowledgment? Start by getting and recreating their world. You know what they are doing. Say it and take the time to speak to its depths. If they are giving their time not only appreciate them for doing that but touch on the many things you are sure they would otherwise be using their time for - this shows a deep appreciation for the gift of their time; you get it and they know you got it. Next, use acknowledgment as an act of creation, meaning, use it to create something for the person that speaks to a life worth living. Speak to the continued growth and depth of their compassion; talk about the leadership they are granting others just starting out; talk about the others who need care and by your example get renewed faith that it's on the way. Here you get to say anything - you make it up! The critical piece is that you speak to a big future. When they hear a future bigger than the one they imagined as a result of your words, they are inspired and know that their present actions are worth it even when it gets hard. Finally, go for the tears - you and them can be crying tears of love and joy at the end of a good acknowledgment. That's connection, that's us being deeply and profoundly human; and, it's delicious.</description>
      <author>Konrad</author>
      <pubDate>Fri, 17 Apr 2009 15:45:21 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-surprising-thing-caregivers-want-most-from-long-distance-relatives</guid>
      <link>http://www.caring.com/blogs/the-surprising-thing-caregivers-want-most-from-long-distance-relatives/comments</link>
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      <title>Comment on Anti-Cancer Superfoods: Do They Really Work?</title>
      <description>well I have had stomach cancer for six years,rather than have my stomach removed(only option)I went for the build up the immune system bluberries every day no red meat get to the gym relax no stress.develope a sense of humour,I call it the laughing cure,in fact everything I read that helps the immune system.ginger,dark chocolate etc.now I feel glad I have cancer!I have never felt so good, if I die tomorrow it was worth it, but it was hard work getting here.  </description>
      <author>octoman</author>
      <pubDate>Fri, 17 Apr 2009 15:05:37 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/anti-cancer-foods</guid>
      <link>http://www.caring.com/blogs/anti-cancer-foods/comments</link>
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      <title>Comment on The Surprising Thing Caregivers Want Most From Long-Distance Relatives</title>
      <description>You have got to be KIDDING!  I need relief! If not physical, but money to help relieve me so I can get away without having to go shopping for the love one.

Not being selfish, but I really, really, need some me time, not a vist for the day from othe sibbilings that don't want to addmit that mom is NO longer mom!</description>
      <author>gberryOK</author>
      <pubDate>Fri, 17 Apr 2009 13:56:54 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/the-surprising-thing-caregivers-want-most-from-long-distance-relatives</guid>
      <link>http://www.caring.com/blogs/the-surprising-thing-caregivers-want-most-from-long-distance-relatives/comments</link>
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      <title>Comment on Watching Dad Dodder: How Much to Help (to Prevent a Fall) and How Much to Leave Him Alone?</title>
      <description>I just visited my mother's doctor with her.  He discourages use of a cane because they usually don't provide enough stability to halt a fall.  &quot;False security,&quot; he says.  Even though pride is a tough subject, he advises a walker AT LEAST for home, where the majority of falls occur.  Mom listens to him better than she listens to me...when she listens at all.  Good luck!  Someetimes I feel like I should bookmark this site for MY kids, since I'm getting close!</description>
      <author>jjobse</author>
      <pubDate>Fri, 17 Apr 2009 01:58:54 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone</guid>
      <link>http://www.caring.com/blogs/watching-dad-dodder-how-much-to-help-to-prevent-a-fall-and-how-much-to-leave-him-alone/comments</link>
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      <title>Comment on Second Opinions: If in Doubt, Seek One Out</title>
      <description>Dear Sarah it is a wonderful story, me being eighty next year I feel an affinity with her,I had a second opinion after  both my consultant and surgeon behaved like clowns.I was sent to a liver transplant surgeon he had my scans on his wall,&quot;the clowns refused to show me them)my liver had several growths both kidneys had growths, and a growth in my stomach(I suppose the clowns thought I might have a heart attack if I had seen them?)any way I had a PET scan that showed only the stomach growth was active,the surgeon was very information he was going remove my stomach with its resident cancer and go into liver to check that,I might not survive the operation,but it was my only option,I could not have drugs,they were reserved for patients who could not have surgery.I decided at seventy three I would rather face cancer with a stomach.I am very well,but I feel so sorry for people who die of cancer,or is it the treatment that killed them?I will not go in to what my clowns got up to it was unbelievable.well just one or two.The consultant always told me my cancer was in my duodenum and persisted to do so for over a year(they decided I was in operable until I did not die) until I question him exactly where?he moved that cancer all the way up first part of my small intestine,and it was'nt there,so I said &quot;it must be in the stomach then?&quot;&quot;Yes&quot;he said.It turned out he thought patients were too stupid to understand!The surgeon was going to remove my cancer by keyhole surgery?my curiosty saved my stomach,I just managed to stop the epidural injection in time. The surgeon was about to remove my stomach without my consent!I could have died a rich man.laughter is the best medicine.isn't it?    </description>
      <author>octoman</author>
      <pubDate>Thu, 16 Apr 2009 15:19:52 -0000</pubDate>
      <guid>http://www.caring.com/blogs/caring-currents/second-opinions-if-in-doubt-seek-one-out</guid>
      <link>http://www.caring.com/blogs/second-opinions-if-in-doubt-seek-one-out/comments</link>
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      <title>Comment on How to Get Someone You Love to Quit Smoking (And Why It's Not Too Late)</title>
      <description>I quit almost 2 years ago cold turkey.  I was 55, but as yet, I had no known health complications from it, I just knew time was running out.   I had tried the patch, they fell off.  Gum made me nauseous.  Friends had had some strange side effects from the drugs including the newer one (Chantrix gave my SIL hallucinations and hot flashes.  At 55, there was already enough of that going on.)  
A site called whyquit.com helped me most.  They support the cold turkey method totally and support those who are ready to try.  I read there for about 6 months and the day came that I simply smoked my last cigarette and did not buy more.  It really was not so very bad, it was free, and it is the most successful method.