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There definitely are funny moments with Alzheimer's and, horrible as the disease is, seeing the humor that occasionally comes from it is a good thing.
When my uncle, who had Alzheimer's, was still alive, there were always things we could laugh about. It was definitely a relief to have some light-hearted times.
One of his funny quirks was that he couldn't stand having lights on in the house, except the ones he needed so, for instance, if my aunt was washing dishes and had the light on in the kitchen, he would yell at her to turn out the light, and she'd have to finish the dishes in the dark. It was just constant -- she'd turn on a light, and he'd yell, "Are you going to turn off that light?"
When he was in the hospital, dying, after a stroke, the nurses had turned on the light over his bed and one of the last things he said to my aunt was, "Are you going to turn off that light?" Even though it was a terribly sad time, it made us all laugh.
Carol
You are so right! Sometimes, you just have to laugh, as you will see when my new book, "Support for Alzheimer's and Dementia Caregivers: The Unsung Heroes," comes out in the Fall, I hope.
A sense of humor is a great way to cope with some of those unexpected moments.
Judy
When I was away, I called him on the phone and he didn't answer. So I drove to my next destination and called again, then he answered. The next day I was sitting in my chair dozing. He kept trying to tell me something about the TV remote. I said, "I just don't understand what you are trying to tell me." He had the remote in his hand and said, "There is no way anyplace in this house that you can answer this. I just kept saying 'hello' and pushing buttons, then I turned it over and looked at the back and I couldn't answer it." I said, "Well, your're right!"
I used to journal, but I don't think I want to write down all these things that happen. It may be funny to someone else, but very sad to me.
Kathy
Do you think your mom realizes that something is wrong with her? I think that must be the hardest stage of Alzheimer's, when the patient knows that her brain is failing her. In some ways, it must be easier when that awareness is gone.
Don't feel guilty about being impatient with your mom now and then. You're under a lot of stress, and it's to be expected that your patience wear thin occasionally. As you say, you just have to stop, take a deep breath, and realize that she's not being willfully difficult.
You seem to have a great attitude about everything, and I'm sure it will help you a lot as you go through this.
I don't know if I have any good advice for you about you mom's smoking and eating habits, but my uncle was just the same. He would gladly have eaten nothing but sweets, and he chain-smoked. My aunt use sweets to bribe him to eat other things. She'd make him a somewhat healthy meal and tell him if he finished it, he could have a piece of cake (or whatever) for dessert. It seemed to work pretty well for them, but don't know if it would for you mother. Maybe it would be good to make an appointment with a nutritionist.
You may already know this but, if not, it might help explain why your mom doesn't want to eat better. Alzheimer's patients often lose a lot of their sense of taste, so most food other than sweet -- and, perhaps salty -- just doesn't taste that good.
Exercise is a really tough one -- it's something my aunt never had any luck getting my uncle to do. He absolutely refused to do anything more than walk to and from the car. Does she like to dance? Maybe the two of you could just dance around the house every now and then.
The smoking is also very difficult, I know. What probably won't work is trying to explain why she needs to stop, or pleading with her to stop, or trying to reason with her in any way. What finally got my uncle to stop was when his doctor put him on the patch and told him if he ever had another cigarette he would end up in the hospital. He never had another cigarette after that, after smoking for close to 60 years.
The bottom line, though, is that you may not be able to get her to do things she doesn't want to do. Her mind works a lot like a child's, so explaining why she should do those things just doesn't get through. Again, I can only go by the experiences we had with my uncle, but telling him to do something always worked better than asking, or giving a choice, or explaining. That's not to say it always worked, but it was more reliably effective than anything else. Given a choice, an Alzheimer's patient is probably not going to choose the thing that's best for him/her so, unless it's something minor, it's probably best not to give her a choice at all.
I don't know if any of this is helpful -- caring for an Alzheimer's patient is an awful lot of trial and error.
We're glad you're here, and hope you'll continue to keep us posted.
Carol
I am a caregiver along with my 85 yr old mother for my 87 yr old father. Are the people that your mom runs to family or friends? The only reason I ask is that there may come a day when you welcome others support and help. I stay with them 24 hours a day 7 days a week for the past 3 years and when others come to help and give me or my mom a break we welcome it. My dad used to burn his cloths, follow my mom everywhere in the house she went including to the bathroom. He fell over 20-30 times every time one of us was no further than 10 feet away. There are 100's of things I could mention but I would have to write a very long , very sad book. He has had Hospice 2 times in the last 2 years after we tried the retirement homes only to realize that if he was going to have any quality of life it would have to be at home because Alzheimer patients do better when at home with familiar surroundings.The bad part is that it's very hard on the Caregivers. If you have others willing to help I personally would gladly accept it as needed. I thought after many things that I had gone through in my life I could handle it much better than I have. When the man I have always looked up to as my hero and a family man that could not have been any better of a role model changed into a man that only looks the same as he did a couple of years ago. I have found that talking to him about things from 20- 40 years ago give us something to talk about because trying to talk about anything in the last several years he doesnt remember. The best way I deal with all the things he says that make no since at the time is to just GO WITH IT . In other words agree to whatever he thinks he see's or whoever he thinks is in the room talking to ( Usually its his mom that passed away 25 years ago or a former coworker from 30 years ago) or talk about old cars. That helps me deal with it and keeps him content and happy for short periods.The one person that I hate having to go through this the most is my mother, she is 85 but does more than most 40 yr olds I know but it has starting taking a toll on her. She knows her health would be better if dad was at a retirement home that would take care of dad like we do at home but the sad truth is they dont have enough staff to watch over him 24/7. I live 300 miles away from my parents and have only spent 3 months at my home out of the last 3 years so I really understand how hard the caregiver job is. I know my dad would do the same for me so I have no regrets, just a lot of stress. I wish you and everyone else in our situation the best dealing with this situation. This has made me think about so many things in life that I took for granted so something good can come from this. God Bless!
The situation with your dad sounds really sad. It's awful to see someone you've loved your whole life gradually disappear. The fact that Alzheimer's patients retain old memories for so long is a real blessing, though. My uncle used to love to talk about the past, and it was always amazing that he could remember names and places that nobody else could come up with.
I just wanted to address one thing you said in your post, regarding Alzheimer's patients being better off in their own homes. I had always thought that, too, but I talked to an Alzheimer's case manager who said that's not usually the case. She said that the transition can be difficult but that patients usually flourish in a memory-care facility. They are with people like them, taking part in whatever activities might interest them, and given expert care by people who have a lot of experience dealing with dementia patients. They often end up very happy in a new place. Dave, one of our regular posters, has found that to be the case with his father.
I bring that up because it sounds like it might be a good option for you and your mother to consider. You're right that your mother's health has to be a big consideration in whatever you do.
I hope you'll continue to post her, and let us know how things are going.
Take care-
Carol
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