Early Alzheimers: He thinks he can do things he no longer can
First, I want to say how much I appreciate this group. It is always a comfort to read the stories here. It makes me feel not so alone. My husband has been diagnosed with MCI due to Alzheimers. His abilities are starting to decline and he has almost no immediate memory. He will ask me over and over the same things 3 or 4 times in 15 minutes. He is still driving and doing okay with that locally, although he does sometimes get lost now even going to familiar places. My biggest problem is he still thinks he can do everything he has always done. He does not realize how confused he gets. He could not really live alone anymore. How do you help a person understand that they need help. He wants to take a trip to meet someone to fish and the drive would be 3 hours. I am still working and unable to go. When I told him I did not think it was a good idea he got very angry and suggested I stop telling him what to do. Then he said I could just leave. The other day he wanted to fix the electrical part of the garage door opener and since it was dealing with electricity, I told him I thought we should get an electrician to do it. This is something he could have formerly done. He asked me if I thought he was an idiot and blew up about that. I can answer questions all day and listen to the same stories over and over, but I do not know how to handle his anger and keeping him safe. I would appreciate any suggestions.
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@rebeccagrover gosh, reading this makes me wonder how I would handle the "moving in and out of Apple Pay" - with short term memory loss, from what I've seen with my husband, you don't want him moving any money, anywhere. You can't be locked out, as if something happened to him, you need immediate access. I've been on my husband for us to "BOTH" do the bills, as I keep telling him, if he was to pass first, he has to show me what to do, to make it easier for me, or I would be stressing over how to do it. It's a bit of a stretch in the "I wouldn't be able to do it." Of course I would, but I don't know how to get him to give up control, so I'm making him think the problem is me. I created a typed sheet of all of our bill pays, and another sheet that shows Auto pay, etc. since he has a "ratted up book, I can't even read......He thinks the book is great, meanwhile, missed payments, double payments, and mistakes we find out about three months later. So, I've really had to get involved with any money transfers anywhere. PS, I keep tellling him, my getting involved has more to do with me, than him since we're up there in years, and if one goes before the other, we need access. Best, Karla
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5 Reactions@kjc48 thank you for your thoughts. I appreciate your ideas very much. Its a hard situation forsure!
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3 ReactionsI know that's why all of collectively together help each other - and that's the way it should be, because it's hard to talk to friends, that aren't dealing with this situation. I find some of mine are just uncomfortable talking about it. Take one day at a time, that's all we can do.
Best, Karla
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4 ReactionsWow,sounds all to familiar. When. My husband attempts not safe jobs I will try and stay with him,but I cannot always do that. I try and distract him,and eventually he moves on to something else
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3 Reactions@kjc482 months ago my husband finally realized he could not pay the bills,So many mistakes . Past due, collection agency etc. and the money was there, he just became very confused. Now that it is in both are names we are back on track. It very much surprised me he agreed letting me tack over . It will eventually happen.
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4 ReactionsI could have written your post six months ago. You feel like you need a crash helmet on at all time.
Dementia has no rhyme or reason and I feel like I live with a preschooler.
I get annoyed with the constant interruptions with orders to look at a bird or event happening in our neighborhood. My husband taught shop classes for over 20 years and slowly could not do simple tasks around our house. He is at the point now where he does not realize that he was ever capable of doing said tasks.
My husband is not as angry as he used to be. He has not threatened to leave me or shout in the past few months. I am going to enjoy this stage, not knowing what the next stage will look like.
I do tire of him showing me pictures or telling me things multiple times a day.
Two doctors and a lawyer told my husband that he could not drive. My husband is upset about, but surrendered his license on his own. I am trying to get used to being the primary driver.
This forum and the UPCAP support groups are fabulous and help.
I keep reminding my self that I am in this for the long haul and to put my seatbelt on.
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9 Reactions@upgirl2013 Oh gosh, it's been such a horrible day, and I'm usually Ms. Positive.
Really, horrible. But I laughed out loud when I saw we feel like we need a "crash helmet." Amen, maybe that would cover my continued bald gray head. Yes, put our seatbelt on. My husband wants to show me birds too, what's up with the brain and birds? Right now, I just wish one, two of three of you were here at the table with me, trying to figure this all out. Thanks for being there, every one of you. Karla
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8 Reactions@kjc48 yes, I feel like I need to start a play group for the patients and their caregivers. We could have coffee and discuss strategies and find humor even on bad days.
We have a dementia group here in town, but my husband is not at the point where he would agree to go.
I am fortunate that I can be away from home for half a day and my husband can make himself a sandwich.
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6 Reactions@rebeccagrover
My heart goes out to you and all the others struggling. My husband diagnosed about 5 months ago after prostate cancer. He now gets angry if you question what he is doing. He has left for an hour and returned and apologized. This is a very difficult disease. I really find comfort I all the suggestions from everybody!! Thank you and wishing you all strength
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7 Reactions@kmarkham sending you hugs for whenever you need them.
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3 Reactions