How can I help my dad, who has Alzheimer's, communicate?
If your dad has just been diagnosed with Alzheimer's, he may feel stressed when he can't find the words he's looking for. Word-finding difficulties are one of the early symptoms of Alzheimer's disease.
Just try to help in an easygoing way. Say to him: "Let's see if we can work together and figure out what you're trying to say." Talk in a calm, gentle voice. Reassure him: "I think you're just anxious. Even when I'm anxious, I can't think of the right word." Or make light of it: "It's probably on the tip of your tongue. You'll remember later."
If you think you have a gist of what he's trying to say, ask questions that might trigger what he's getting at. Even if he's using the wrong word, it can give you a clue to what he's trying to say. Sometimes people misname things. You could say, "Do you mean…" and supply the right word. But watch for his reaction—sometimes too many prompts leave a person feeling frustrated.
If you have no idea what he's talking about, try to change the subject or redirect his attention to reduce his frustration. If it seems important, you can return to the subject later and try again.
I am the patient. In recent days when I proof read something I have written (thank Heavens for computers), I notice a word that absolutely has nothing to do with what I'm trying to say. That is, I substitute a word with a completely different word. It was a blow when I couldn't crochet or cook much. But it is REALLY going to be a blow when I don't have this communication tool. I'm on Namenda and Aricept. Am I right that there's really nothing I can do to make that better? I'm wondering now if I do this when I talk and my family covers for me. They say I don't. I know I've been having a problem being understood, which I knew was going to happen, but for now it's still tough. I've been searching for words, and sometimes they just don't come to me. When I've had that happen someone either supplies the word or says they know what I'm trying to say. That helps!
Oh my gosh, I'M NOT ALONE Please respond. I thought this disease was so different. My dad can't say what he wants to,but it's there. I so I was so alone. Tks for being there.
No, you're not alone. There are a lot of us out here.
I can see where this would be hard for the caregiver to know what to do--it's hard on us--we get so frustrated with ourselves when we can't remember a word, or forget what we were talking about. I've often wondered if that's why so many patients quit talking. I'm gonna hang in there on that for as long as I can! I don't mind at all if someone can help me with a word--because with me if I can't figure it out, it's not going to come to me even with prompting.
This site is a good place to find answers, or at least someone to talk to if you have problems that are bothering you like this. Altho I think I'm the only patient in the group, it still helps me know I'm not alone, others are feeling what I'm feeling, or having to deal with it, like you!
Have a good Saturday! Chris
