Follow
Share

Hubby has been in MC for two months. He's more cognizant than most other residents and well aware that he's "not like them." However, I do notice him slipping more and more. Every time we talk, he keeps insisting he's coming home as soon as he finishes six weeks of PT for post-op back surgery. He keeps confusing that with his dementia and goes back and forth with his stories. Point is.... I can't really put him off with fiblits because he's too aware. Now he's reading articles on the internet that he swears back him up that HIS dementia is not going to get worse, and he'll live another 10 years (to 93) and die in his own home. He doesn't ask, he INSISTS. I've given up with the "explaining" (I know... it doesn't work) but the fiblits don't work either and now I just remain silent. Now he's accusing me of not wanting him home, which is true because I was sole caregiver and his decisions and outbursts were getting dangerous. There's no WAY I can go back to that, but I face either a knock-down-drag-out fight (that will hurt him and he may not even remember), or this repetitive aggressive stance he's taking that makes me dread talking to him. Any suggestions of what I can say or do?

This question has been closed for answers. Ask a New Question.
I'm sorry you're going through this. Sounds really hard. It's a challenge to get someone in the right level of care at the right time. I'm sure it's very common to be too good for X and too bad for Y. How often do you visit him? Maybe you could back off on the frequency so that he can better adjust to his surroundings? He won't like that but it could be good for you. You could use a fiblit to say that you're not feeling well and don't want to get anyone sick. I would say I have a 101 temp and need to stay in bed for a day or three until feeling better.

Maybe have some vague responses ready like "we'll see how it goes" or "I'm not sure if that's a good idea at this time". Acknowledge that it's hard for him, etc.

Good luck.
Helpful Answer (4)
Report

I might encourage him (and staff too) to have him volunteer at something to know that he is helping people who after all, maybe do need more help than him. And/or an activity that he's gonna be very good at and that exercises his mind.

This might be sorting nuts and bolts or passing out Bingo cards. Whatever it is, he will feel like the "boss" likes him, that he's useful and that he's appreciated.
Helpful Answer (3)
Report

It may be time to tell dh that his doctor says he needs to stay where he's at for the next 6 months at which time he will review the situation once again. Blame his doctor, then tell him you're not feeling well and will be staying home for the time being and not visiting. In the meantime, speak to his doctor about his agitation to see what he suggests. Stop visiting for a few weeks and give both of you a chance to relax and take a break.

When my mother's dementia advanced and she began demanding I take her home to live with me, I let her know that was impossible due to her myriad of health and mobility issues that I could not possibly handle myself. That was the honest truth of the matter, too. I repeated myself as often as necessary and eventully, Ativan was prescribed by the doctor in low doses when her agitation increased and became aggressive. It helped her a lot, thankfully, and she relaxed quite a bit.

Call the nurse to see how dh is really doing on a daily basis and if he can be given a daily job, like Peggy Sue suggested. You can't really "do" anything about this situation but the MC can help him out, along with his doctor. It also takes time to adjust in MC, especially for a person who doesn't see themselves as having an issue that requires them to be there in the first place.

Dementia is a no win situation for everyone, isn't that the truth? You can't bring him home for obvious reasons, so give him a chance to adjust and ask the staff to give him a job.....that should help.

Best of luck
Helpful Answer (4)
Report

I hope you'll be all right. And your husband too.

It's difficult for sure, for both of you.

Does your husband have money? Is there any chance he could live in a small place on his own, with a caregiver? That costs money of course. But so does living in MC.

If your husband is horribly unhappy in MC (and his mind is "very aware"), and if it's at all possible, maybe he should get out.

We ourselves might not realize how terrible it can be to live in that specific MC. That particular MC might be wonderful. But, it might be a feeling of being imprisoned.

Many of us have been in hospital for a few days in our lives. We know the feeling: we can't wait to go home. Some people have experienced being in a facility (even a wonderful facility) for a short while: they want out. Not everyone wants out. Some people do.

It's extremely understandable that - you - can't care for your husband in your home. It's too much. It was destroying you.

Can he live somewhere else?
In the future, if necessary, he can return to a facility.

You know your husband. You know the full picture.
What would you want done to you, if the roles were reversed? Maybe you would want your husband to insist on MC. Only you know the full picture, what is best.
Helpful Answer (0)
Report

You may have to be honest. Tell him you love him dearly but you can not physically take care of him. He needs to be where the care is for now.

I would not place him in his own apt with a caregiver. That would mean you are then involved with overseeing that the aide is there doing her/his job. Aides are too unpredictable. And it would mean 24/7 care that would cost as much or more than the MC.

They always want to go home. Its familiar. Those suffering from a Dementia cannot be reasoned with and get self-centered. He is safe and cared for. You don't need the stress that caring for him brings.
Helpful Answer (1)
Report

This question has been closed for answers. Ask a New Question.
Ask a Question
Subscribe to
Our Newsletter