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As a person who myself struggles , with grammar , spelling , punctuation , run on sentences , incomplete sentences , wrong word tense , vocabulary , you name it , I am usually the last person who is the writing police . However , I do believe most times people understand what I am saying without too much difficulty .
I am going to suggest to you punctuation , it helps alot . Many people on this Forum are older and will not even bother to try to read what you write . I found it very difficult and had to reread it more than once .
It would be a shame for you to waste your time , as well as , potentially someone missing an opportunity to learn information from you because your posts are simply skipped and not read .
Due to major impulsivity issues - he lost his mobility scooter access not long after he was admitted to the SNF.
This facility was well designed - surrounded by gardens and when not on flat ground, the grades/inclines were very low - especially designed for wheelchair access.
Taking him "off campus" was entirely up to us -but that was never even on our radar - there was no way we were risking it - he was too big of a fall risk.
So we decided to take him out one day around the campus - we offered to attach the foot rests and push him. He flat out refused the foot rests and opted instead to hold his feet up for the entire excursion ( which was very, very short).
I started to take him down the nearly flat incline into the garden, and he started screaming - so much that I thought maybe his hand was caught in the wheel or something and I immediately dragged all 400+ pounds to a halt (300+ of him and 100+ of the wheelchair). He was screaming "You were about to dump me out. I was about to fall!"
Now, he was nowhere near falling. He wasn't even uneven or unlevel. But he got it in his head that he was about to fall out of the wheelchair. He spent the rest of the time we were outside screaming about going back inside because it was a deathtrap outside.
Now this is a man who HATED being in that facility with every fiber of his being. He made sure we knew it every single day.
But on the ONE attempt to take him out on our own - it was disastrous and we didn't even leave the grounds.
He was taken off site a couple of times, for doctor's appointments and once to the hospital. But each of those times - he was in the wheelchair and locked into the floor of a vehicle, so to him he was stationary. He also had two CNAs for each trip.
But each and every time he wanted to know how much longer he was going to be gone.
I only say that to say this - every single time you move someone with Dementia - you run the risk of hitting a restart button, or causing them more confusion or distress.
Is there a reason you think she would be better off getting out? Are they giving you reasons for not doing so?
After doing that, watch Shawshank Redemption. A little tease if you haven't seen the movie, a prisoner is released to the free world. It doesn't go that well
Even though he didn't have Dementia, what he experienced probably is similar to what many Dementia people experience if they're taken out of the facility.
My MIL thought outings would be good for her mother too. She thought taking her to lunch for two hours would be harmless. It wasn't.
Her mother thought they'd been out of town, and was worried "the hotel" wouldn't let them back in. What is two hours to us, is two days or two weeks to them. When she got back to her room, she'd forget where her bathroom was. She'd take clothes out of drawers so she could "unpack from the trip" or "unpack from moving away". She'd get disoriented and wouldn't recognize her usual surroundings. It took a few days to get her re-acclimated, and that was hard on her.
Routine is VITAL for dementia. A short outing is more than enough to throw them off for days.
Why exactly is she placed in a Memory Care facility?
Why not living with you in your home?
Does she try to wander? Escape? Have meltdowns? Tantrums? Helpless in emergencies? Prone to falls?
Where did she live before the MC facility? Was she safe where she was then?
"I'm sure they are afraid she could get agitated. But she keeps asking 'when can we go out'. I just feel like she's a prisoner."
A prisoner is locked up behind steel bars for committing a crime. Your Mother is very old, with (apparently) dementia that has progressed to sundowning. She is in MC for her own well being and personal safety at this time in her life. She is kept fed, clean and safe, by a 24 hour staff of medical professionals. She is in her new safe haven.
Read what Lealonnie wrote below. What happens when you take her out and she has a meltdown? Or refuses to go back? Better to visit Mom with something nice to share and enjoy quality together at her facility, than tempt her with what she cannot have, and possibly cause her to get upset?
But mom’s brain is no longer normal. She can’t and will never think
normally again. Accept this and follow the advice of her professional caregivers. I’m so sorry, but we have to meet our loved ones where they are, not where we wish they were.
I took my mother home to my house for Thanksgiving in 2019 after she'd gone into Memory Care from regular AL Her dementia was moderate at the time, no Sundowning or other erratic behavior, just her typical anxiety. About 30 minutes into the event, she was ready to leave and "go home." She constantly asked what time it was.....about 230pm if I recall, and she started saying it would get dark soon. It might snow. The driveway might get icy. Her "girls" would want to know where she was. Her meds would be late. On and on and ON she went to The point we ate early and DH took her back to the MC with a bunch of leftovers. She couldn't sit still long enough for dessert.
You just don't know HOW an elder with dementia will act once theyre away from their safe haven. That's the truth of the matter.
It is very common for dementia to ask when they’re leaving or when they can go. But she isn’t seeing this the same way… she says she wants to “go” but she doesn’t know where or why.
So we’d sit on the home’s front porch. Then we didn’t go further than sitting by the window in the common room. And now she cannot leave her room without panicking or becoming angry. (Dr prescribed a calming med)
Is your mother becoming like mine?
And why do you think it would help ?
Are you taking her out for a visit or to move her permanently ?
More info would be helpful.
In general their world gets small and they are more comfortable in their familiar space and with a routine.