My parents live in a four story home. Actually they live in the chilly, dark dungeon of a basement in a four story home because my father cannot walk up stairs. There are stairs between the basement and garage and the bathroom shower has a curb. He has PD, extremely poor balance, and cannot walk unassisted. He refuses to use a walker, rollator or wheelchair. They have had doctors, therapists, social workers, friends and family tell them that the home is a death trap, but they will not move. My mother thinks he will get better and my father just goes along with it. My mother who has hoarding tendencies has filled the upper stories with piles of papers and doodads and junk she still buys by the carload. He has had many falls, bruises, cuts, broken ribs, and black eyes but acts like it was nothing and my mother refuses to acknowledge that he has fallen more than once or twice. Always she has some ridiculous excuse to explain it away. They should be in independent or assisted living, but insist they are too healthy. I tried taking them house hunting for a more suitable home, with a first-floor master bed, kitchen and garage, but after weeks of that realized they were just humoring me and have no intention of moving. I just have to wait for something so awful to happen that they are forced to move, like to the hospital and then to a nursing home. It is hard to accept there is nothing I can do. When I talk to relatives I feel like it is my fault that they will not move. How do I find peace with their decision to live this way? It is like my parents want the whole family to watch while they are tied to a train track with the train just around the corner, whistling.
but cannot afford help to come in or to redo a shower?
Changes to be made to that budget, I am guessing.
How to step back......hmmmmn.
I'm only 55 and am stuck in my ways. I hate change. I had that blanket when I was a toddler. Old, ratty, torn, probably smelly too. My Mom was smart though. She bought me a doll. It was called Teary Deary Doll. She managed to slowly get me to attach to it. She tossed out my Banky as I called it. Then the Teary Deary Doll was replaced and so on and so on. Maybe that's an idea for caregivers. Don't make the change an all or nothing thing right off the bat. Just start with small changes and gradually work up to the big ones. Of course, time is a factor when you are dealing with health/fall concerns with elderly people but maybe for future caregivers whose parents are not at that critical stage yet. Gradually implement the changes.
Maybe, someone else on here has some ideas on little changes to start off with and so on and so on. Food for thought anyway.
Love coming here to grab some smiles in the midst of it all!!
A Little Debbie sounds good right about now...(after I eat my 2nd bowl of ice cream for comfort)
Aging is such a gradual process. My folks have been looking at this old crap their whole lives, and don't have the slightest idea there's anything wrong. And they don't understand why I can only stand to stay a few nights when I visit. Oh, and they haven't opened a window since the Johnson administration.
I wonder if this isn't the most common complaint amount caregivers: Waiting for the boiler to blow on the slow motion train wreck. I've been thinking it'll happen any minute for 6 years. It can wear you down if you let it. I've had to detach. Accept that there will be a blown boiler.
I know they don't eat right. I can't get them to eat decent food even when I'm there. I got mom an electric lift chair. She struggles to get in and out of it and uses her control button only to raise and lower the footrest. Drives me bug s...t! She's too vain to use the electric scooter at the grocery. So she just doesn't go, sends dad, with dementia who can find milk, Bologna, cheese and little Debby's and that's about it.
When I visit I always stock the fridge with some fruit, salad in a bag etc. and then throw it all out on my next trip home and then sit down and have a couple little Debby's with Dad.
Well said Countrymouse.
But I don't find it that baffling. Unless your home means nothing to you, is it really so hard to understand why elderly people who've lived in one place for decades are reluctant to give it up? It's like the child's comfort blanket - ragged, smelly, colourless, of no use or ornament and decidedly unhygienic (unless you can sneak it into the washer while he's asleep) - but incomparably precious. There are lots of beautiful homes in the world, of course, but if they're not yours they're just not the same.
The term "living independent" needs to be changed. It's not exact especially when we are the ones doing most of the things so that they can be independent. Something is very wrong with this picture.
they're on their own.
As for me, it was actually her firing her in home aide and the police being called for her to finally give in to assisted living (which only after a month became memory care). I know she needed the help, put it had to go that way. You can't feel guilty, trust me it doesn't get easier once their are in an ALF, Memory Care or Nursing Home.
I'm sure my brothers would love it if I would volunteer to be my mother's home health aide (be there when she showers) and housecleaner. I refuse. I don't want to do for her, because she has made it quite clear that my time is worthless. No appreciation = no service. I was roped into becoming her taxi service, and had to set strict boundaries for that.
One of my brothers visited her this past weekend. He said it's like she lives in a prison. It's stuffy and dark (she keeps the blinds closed). It's her choice, though.
She talks about assisted living, but we know she's not serious about it. When the fall happens, she will be hospitalized, then in rehab, then in a facility that she will have little to no say in choosing. And under no circumstances will I agree to provide any care so that she could remain in her condo.
I know this must be so frustrating. I do wonder about something you said in your first post. You said that when you talk with relatives, you feel that your parents' refusal to move is your fault. Can you explain? I don't understand this. It there something the relatives are saying that causes you mto feel this way?
I might also add that while not visiting the house is a good idea in one way, it might deprive you seeing when the situation makes a turn for the worse. How are they at taking medications, avoiding spoiled food, proper hygiene, bathroom clean? If they can't really maintain their own household, it might be some evidence of incompetence. I might consult with an attorney in their area to see what evidence you need, IF you were to attempt to take legal course. That way, you know what is required. Sometimes, poor judgment is a first sign of cognitive decline and not memory loss. Sometimes, courts consider the ability to keep one in a safe environment, free from dangers, etc. I'd find out the standard in their jurisdiction. Plus, what does their doctor say? I would think the doctor would be quite concerned.