How do I deal with overbearing Alzheimer's care?

4 answers | Last updated: Jan 14, 2012
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Caring.com User - Joyce Simard
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A social worker and geriatric consultant who specializes in dementia care, Joyce Simard is based in Land O' Lakes, Florida, and in Prague. She...
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Joyce Simard said...

This behavior is not uncommon. The well spouse trying to have some "control" over a situation where he has no control because of the disease is a difficult situation.  No See also:
What's the best way to handle criticism about the Alzheimer's care I'm giving my mom?

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magic answer but here are some suggestions.

Ask her physician to become involved. Try to get him to attend a support group. Perhaps have someone take him so you know he really goes! See if he will agree in writing to a certain schedule for her so he can be reminded what he has agreed to. If only you could get him involved in his own activities but from experience i know that is tough. When she slips into the advanced stage of dementia he may want medical interventions that are more of a burden than a benefit. He is fortunate to have such a caring social worker!

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LindaSD said...

Very insightful post. Yes, what a caring social worker. It makes me think that this is probably an issue for a lot of healthcare workers, even in a normal patient setting in a hospital, especially when dealing with the very elderly patients. In reality it is possible for both husband and wife to have diminished mental capacity when only one is being treated.

Would there be a good healthcare, professional support group - if not maybe worth forming some network that offers help.

As a caregiver to my mother who has Alzheimer's, I will keep in mind my demands on staff when in these situations. I remember when my dad went into the nursing home for late stage Alzheimer's, I was not always patient with the social worker there. It is a very stressful time for family.

I guess I would ask, in the end, even though you feel the wife is not getting the care she needs, maybe, just maybe this is "their" end of life experience and you are along for the ride. Maybe as hard as it is for you and staff, you can find a way to support him different than normal. Is there a way to have a staff member be part of his visits and bring the activity to both of them? Just thinking outloud from a non professional point of view.

You are a very kind and caring person. What a tough job. Thanks for caring so much.

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A fellow caregiver said...

What is the difference, if any, between Primary Progressive Apshia and Alzheimer's. Does the first always lead into the other & how can you tell what the patient is really suffering from?

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I am curious as to the outcome of this particular situation as it was posted a couple years ago. We can all learn.

However, because similar behavior will surface among other couples and family members, THE KEY IS for the social worker to LEARN AS MUCH AS POSSIBLE ABOUT THE doctor and his FAMILY dynamics from family members.

One never knows the reasons why people do things--

-- the doctor feels guilt for his wife's Alzheimer's and this is the price he pays. -- he perceives she is not receiving the kind of care he is able to provide (whether or not this is true, this may be his perception).

On the positive side, this could also be his remaining loving act of grace for his beloved.

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