Dad (83) has dementia and Parkinson’s. Limited mobility. Mom (79) has been primary caregiver, but recently we have been adding home caregiving to help with ADL’s. Mom adamant about not sending Dad to memory care. Yet she’s getting irritable and weary of caregivers in her home and invading her privacy. I’ve told her she can’t have it both ways. Too much risk of her trying to manage on her own. They have the monetary means for home health. The adjustment is not going well!
Tell mom this situation cannot be fixed, and she doesn't have to be dancing a jig about it. She just has to accept one of the 3 choices and live with it, as we all have crosses to bear in life.
Go shopping, have lunch with a friend she has not seen in a while, get her hair done.
A few hours at the Senior Center playing cards or even volunteering there.
It is great to have caregivers come in and help out but part of having that help is to get away from the house.
Does mom have a friend or relative she can go visit for a week? Maybe a week Respite for mom would be a good thing.
Memory care isn't a torture chamber. The facilities are set up for with an eye to keeping residents happy on their level. The people who dedicate themselves to this care are kind, caring and loving. Mom can visit often. They may pamper her too. Win win.
My brother-in law is in a small home in a residential neighborhood and has been there for years. He loves it. My sister-in-law (no relation to brother-in-law) is in a larger one in another state. Her husband visits every night for dinner and volunteers to lead classes for residents. She likes to garden and they have raised beds so she can do that with assistance. The caregivers give her fancy manicures. The owner's dogs visit often. Both of these relatives were languishing at home and have benefited immeasurably because nobody was "adamant" that they stay at home miserable home.
i tried all the suggestions listed here — telling her when aides arrive, to go to another room, go out, just get used to it, she has no choice between this and residential care, she can’t leave him in his own waste to get bedsores, it was pretty much elder abuse, etc etc.
Eventually it reached a crisis where I insisted he go for a 5-day respite stay because her mental health was terrible, my life was a wreck, she was calling 911 frequently just to get him up off the floor when I was at work and he fell and I knew he was not getting any better. He ended up passing 3-4 days later in early May at the residential hospice place. She got her wish of keeping him at home as long as humanly possible. I was pretty traumatized by some of the things I had to deal with because she couldn’t and wouldn’t let the aides be there. She actually said near the end that she couldn’t believe the hospice would leave her alone with my dad. I replied they have been urging and begging you to have full time aides here for months and you keep getting rid of them!
I have had two friends tell me their parents hated in-home aides for invasion of privacy but they somehow adapted much more easily to residential care. Doesn’t seem logical because it’s more change, but maybe it’s true.
I feel for you deeply — just know you are doing the best you can. It is so hard to know what is best. You don’t want to force them and yet there are really only two options. In home care or some flavor of residential care.
good luck and best wishes!
But this is not your problem to fix. It's mom's. If she complains to you, I say, "what are you going to change to make it better, or is this simply something you're going to have to adjust to?"
Is there any chance mom would consider Assisted Living for both of them.
Normally I would not suggest anyone with dementia for AL but with mom there the keep an eye on him it might work.
She would get more help.
Dad could transition to Memory Care. Or spend time there when mom wants to go on an outing or go to an activity.
This might also solve a problem of getting mom help when she need more help rather than relying on you or other family members.
We tried several different caregivers before we found the right ones for us. The key for us was to find a caregiver who is a natural introvert....quiet....competent....knows what to do and remembers how we like to have things done....friendly but he doesn't try to constantly engage with us with obnoxious "make-nice" chatty conversations unless we initiate a conversation with him ourselves. We've come to enjoy his quiet and helpful presence here.
We do everything we can to make sure he's comfortable working here and we respect his privacy, too.
Good luck finding a competent caregiver who meshes with your household style.
I read one comment about home health aides being unemployed losers. They're not. These people are part of a care team with a plan of care that must be carried out during the time spent with the client. Yes, I do understand there are some bad eggs in the batch, but these are far and few in between. The care plan is given and must be charted during each visit. All of this is explained to the patient and the family member during the initial nursing assessment before placing a worker in the home.
The hired caregiver stays in another room until Dad needs something ?
This way Mom stays clear of the caregiver . Does Mom drive so she could leave for a few hours, or even go outside for a walk ?
If Mom doesn’t get used to it then memory care it is. You are right , she can’t have it both ways.
I suspect Mom’s weariness it not just from having strangers in the house. Living with your father’s conditions is most likely causing weariness as well .
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