My 93 year old mom has been in a big memory care facility for 7 months and is having a rough time with all the commotion and unchecked behavior of younger Alzheimer's residents.
While she's not bedridden she has had many falls and several compressed veterbrae
I don't want to move her to a nursing home but need to make a change away from from where she is as it is unsafe and what too expensive
Nursing home, though, are not JUST for bedridden patients. My mom was ambulatory when she was admitted. But her CHF and various pulmonary problems qualified her medically for NH care.
Mom just takes a BP med and a diabetes pill - we check her A1C every 4 mos
Given her bad back I'd like to keep her in her own comfortable bed as long as possible
When I moved my cousin from regular AL to a small Secure Memory Care AL, I looked online at a list of all the state licensed memory care facilities that were in reasonable driving distance from me. I narrowed down the places, including some home boarding type places, called and even went to visit some in person. Those home boarding places are normally full, but I didn't have the option of getting on a waiting list.
Have you considered a small Memory Care facility or one that is a wing of a larger AL? The one I found is small and family owned. It's not perfect, but, I don't have that many complaints. She tells me she likes it there and that they are all very nice. Plus, the rooms are super large.
Thanks- I realize there's no place like home but I need to move her for both financial reasons and her safety - she has told me she can't take it there anymore - I have visited three other memory care facilities which are smaller than her 62 bed facility now but didn't find them appropriate - she primarily needs custodial care but because she is difficult to handle with the dementia even on seroquel I'm afraid she won't last anywhere for long
Her doctors have no suggestions and just say there aren't many choices
While my siblings have completely walked away I can't and won't and she still wants to enjoy life so I'll still fight to give her a chance
Just that extra attention to some positive individuality gets them to treat him better I think. I don't like usual facilities - group oriented care is very demeaning, especially if it's all the time. I don't like the model - the meds make it easy for staff to not have to brainstorm about what changes could make things go better.
I don't know if it's possible for you, or if it would help, to hire an aide from outside, who could go regularly - and if not an aide, someone who can be regular for 3 hours a shift once a week. Some in those programs do hire aides. (I've been hired as an aide to get a pt w Alzheimers up and into the shower in the am. I ended up quitting, when I found the staff focus was on my communication about arbitrary little rules, when I was the only aide who made it my challenge to make sure the woman actually did get up and shower. I started early with her, roused her gently with arm around her, joked with her, let her wake and started talking about shower, then pause, and chat other things, then mention shower positively, and it took about 20 min, and I was inching her towards the bed edge during that time. Then I could say "good, OK, I'll help you up - and guide her to get up and come with me and I'd walk her into the shower room, often ended up as wet as she was, by the time all was done.
I hated that other individually hired aides with the same job would write on their report, "patient refused shower" and they gave up, did not give them, just gave a bed wipe - after I left, that woman got an infection so bad, she needed pain/oxygen hospital for months.
They don't do enough persuasion with attention and patience, much is lost when staff are always rushing.
My brother's facility has great local music, at least twice a month, and the place is small enough, that humanity comes through. It sits on flat land, so my brother can walk outdoors with a walker. I work to affirm their efforts, even if I sometimes complain, say this is not right sometimes, and meet with higher ups, but my goal is to do my best to express that I understand they are busy and challenged, but ask for special help at times, and notice each good thing they do for him, so the interest in quality does come up often enough.
Choose a spot where there are outside visitors easily, including you, and if you can't get there dependably, hire one person, one day a week, to go and do special activities for a couple of hours each week, chosen by you, with your mom.
We are in a suburb of Los Angeles and costs are very high - facility is $300 a day plus $450 a month for diapers - since she fell there in her room during the night I've had private caregivers with her 12 hours a day adding another $260 a day to the tab - if I pull them she will be in harm's way - I visit 3- to 4 times a week sometimes very late at night and put her to bed since they would just let her sleep in her clothes without a diaper and not even have her walker nearby - once it was folded up and put in a corner - no doubt how she fell her first month there
If I could find a nice home for even $6,000 a month I could keep private aides 4 hours a day and pay less than her facility now - she is very dependent upon me and calls my name when she wakes up during the night - it's heartbreaking to me
For a while the they participated in some of the group activities, but after the wife passed, the husband prefers to stay in his room and watch TV and read the daily paper, only leaving to walk to the dining room. He is happy with the new friends he has made there. It was a great relief to find a place with those space options and have quality care go with it. I check periodically with the health administrator and she updates me on my friend's needs and how things are going. I have health care power of attorney and also pay all his bills so I am involved in every aspect of his care, agreeing to it as need change and signing that I do. I am there two times a week usually, more if we have a doctor's appointment or something to go to. I am relieved that my friend always tells me how happy he is there and I have gotten to know and like some of the other residents, too, and we always have big smiles for each other. It's too bad more facilities don't offer this flexibility in apartment sizes for their memory care units. I was able to make their apartment look just like their bedroom and den in their condo with the same furniture arranged the same way. When they moved in, they were happy from the start, never once talking about "going home."