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We were talking on another thread about, when caregivers come into your home and get close to your husband and the wife feels threatened, or more left out. It's all normal human feelings.
Just be happy your husband is being looked after and he is happy. It would be much harder for you if your husband was crying to come home at every visit, and calling you crying all the time , this is a good thing, and I'm sure what your head wants. It's just your heart that's hurting. I can see this being very hard.
Your life together, can't be erased. I have no good answers for you, but it sounds like your doing a great job. Got your husband someplace where he is safe and happier.
This happiness won't last, his dementia will get worse and you will miss the days you walked in and saw him laughing, even if it was with someone else. So be happy that for now he is doing well, and work on your mental and physical health.
Best of luck, wish I had better answer for you
I have seen this on a personal basis with a friend of my aunt's years ago. Her husband believed that one of his fellow residents was his wife, and would introduce the visiting wife as "here's my nice friend who visits".
As I said, this is not uncommon. This is quite common when the dementia has reached the stage where the person no longer remembers family relationships. They may often think a visiting daughter is the wife. The only thing one can do really, is understand that if their loved one has found any happiness that is a good thing. Imho.
This is called Sundowning, a very common behavior of dementia. People want to go home, but not to the home they most recently occupied -- rather most likely a home deep in their long-term memory, a happy place, like their childhood home.
My 100-yr old Aunt with dementia wanted to "go home" every afternoon even though she was sitting in the one she'd been living in since 1975.
It makes me happy to read about your husband's adjustment and contentedness.
Memory care is designed for people with dementia. Life is simplified. There is a routine. Routine can provide stability and comfort. Activities designed for people with dementia help them feel engaged without constant failure and frustration. Extroverts especially like the additional human interaction.
Some people, as they progress in their dementia, can become more at peace, whereas the early and middle stages were full of loss and frustration they were mentally more aware of.
You CANNOT ask for more than that.
Please don't waste your time worrying about why he's happier there than he was at home. Instead be grateful that he's just happy and more relaxed now.
Not everyone who places a loved one in memory care can say the same.
You are blessed beyond measure that he's doing so well! Don't forget that!
He accepts because he is in a place that does not confuse him, it is calming and he has a friend.
You seem at ease with his calmness and acceptance both of his situation and his friendship. Because you are calm and relaxed that helps him know that he and you are both OK.
As I often said caring for my Husband you Mourn what was yet you rejoice in what you have.
((hugs))
With dementia, different parts of the brain are functioning and/or losing cells - meaning that 'we' often do not know the why of how a person with dementia communicates, behaves, understands.
[I had a client for two years who spoke jibberish. Occasoinally, I would say "I have to get something out of my car, I'll be back" and she'd say "Okay" - these moments of presumed clarity didn't happen often and I wonder how / and why they did happen when they did.]
I would guess it has to do with how he processes 'present' time, and how relaxed he might feel with others around him. When he sees you, his mind 'may' go to "oh, I know you ... my wife ... let's go home. When you aren't there, he doesn't think about this as his brain doesn't 'think ahead' to when you'll be with him.
This is a guess.
While you do not tell us the degree or kind of dementia he has, he might be aware of 'all' the staff caring for him and find comfort in that ... it could be medication...
What I hear in your post is that you do not feel any 'jealousy' of the woman who pays more / a lot of attention to him (not that you would naturally or automatically do that - these relationships can / do change due to memory loss). If anything, you are very considerate of her, knowing she is a support to your husband.
It could be as simple as he sees 'lots' of people around and feels safe(r).
We often do not know (if ever) what or how a person's brain processes information / thoughts.
If I were you, I would count my blessings that he feels somewhat well adjusted and comfortable where he is. And, perhaps get a book or two on dementia and learn how the brain functions.
Gena / Touch Matters
I think that the reason your husband now seems happier isn't exactly because of where he is, it's because he's no longer aware (or not as much) of the fact he can't remember or think properly, as he once did. Those troubling, niggling worries have melted away, and he's just in the here and now.
Part of that could be because he's no longer at home, not because home wasn't a nice place, but it kept him tethered to those worries about what he was forgetting. In the care home, those reminders are gone.
Don't feel sad that he seems happier away from you. It's probably because he had loved you and your life together that he was trying to hold on to the past, but it kept slipping through his fingers.
Now, he can just let go.
I hope you also find times of comfort.
The first time we took him out, we wondered if he would want to go back. He went right in. We took him to another facility to see if he would like it better, but he wasn’t interested in it.
I had moved and he wasn’t interested in my new apartment. He didn’t get the best of care, but hospice was a Godsend. He was there 5 months before passing. It was strange to me that he was content but give me a little peace.
I hope with all of my heart that my husband adapts as well as yours to living around nice people who have absolutely no expectations of him.
And yes, I hope there are sweet women there who will bring out the charm that has been buried under years of familiarity and responsibility.
I wonder how much of this adjustment has to do with timing of placement. Seems like maybe there is a window of opportunity that needs to be jumped through at just the right moment and you did it!
I would love to have everyone’s wisdom on that.
I think it is only good luck that means he is happily confused, as the opposite is so often the case for so many.
I would just count yourself lucky in this moment that he isn't agitated and upset.
We can't take anything about our partners with Alzheimer's personally.
It may seem he's happier than when at Home , but really he's just living in the Present and may not be rehashing his former Life of Independence and home-life. You know that were he not burdened with Alzheimer's , and of totally sound mind, he'd be seriously questioning his new residency in a Memory Care Facility.
You, yourself, may be better off observing that he's so content , than had it been the Opposite.