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She has a catheter that she must empty several times daily. She bends over the toilet to do so. I put a hospital chair in her tub so she can empty into the drain with hot water running. The night bag works great for this.


The day bag is more challenging, so we added a fold-up stool to the tub. She can put her foot on the stool and empty the bag into a urinal while sitting in the chair, then pour urinal down the drain. She says it’s faster to bend over the toilet. This is how she fell last time.


I tried to explain that it will become faster to empty the bag into urinal/tub the more she does it. She is now very lightheaded from the concussion. She just won’t do whatever is necessary to assure she won’t fall again. I’m at my wits end. She is in independent living. I’m her only caregiver.

Once there was a couple reaching the end of independant living. Mr Calm & Not Yet Ready & Mrs Staying Home Stubborn.

There was no Fairy Godmother, just a nagging daughter that kept on & on about a Plan B, downsizing, a new stage. Whatever title she thought may work. Made like 30 attempts, probably more.

Eventually wore one down.. after another chat of "So if you HAD to go to an AL, would you prefer the one UP the hill, or the one DOWN the hill? One day Mrs Stubborn forgot to say "Neither!" but said "I guess.. down the hill".

From that day on, light little *jokes* were added.. "You'll get used to it when you move down the hill". "Imagine not having to cook? Or do the dishes?"Or "what lovely trees" everytime they passed by.

Chip chip chip.

Forward to 2024, when the chips DID fall. Crises arrived. Mr Calm & Ready Now made a swift decision & a lovely place was chosen on instinct. But as the crises deepened so fast, 'down the hill' was available first.

The end of the tale arrived for one. Skipped the nursing home stage - straight to endless peace.

The other likes their home down the hill! Enjoys the meals, the activities, the view of the trees.

As happy an end as could be.
💙🕊😊
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Beatty Jun 14, 2025
TannD, may your tale work out well too 🤗
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Assisted Living does not handle catheters as a rule.

What score did mom get on the cognitive exam she was given? I assume it was not a good one or a referral to a neurologist would not be necessary.

That said, your mother likely has dementia which is why it won't register with her why she shouldn't be bending over. My mother was about 90 when she developed vertigo. She started falling and wound up falling 95x between then and when she died at 95+. I took her back and forth to the ENT for the Epley Maneuver more times than I can recall. It'd help for awhile, then she'd be back to "dying" with vertigo. Back we'd go.

You can't expect a 90 year old with more issues than Newsweek to take proper care of herself in Independent Living. She belongs in a wheelchair if the vertigo cannot be managed with medication and an ENT. My mother went into a wheelchair at 92 because of the falls and the fact that nothing stopped the vertigo for any length of time. Except the wheelchair. She NEVER experienced another round of vertigo after she went into a wheelchair, btw. Physical and occupational therapy didn't work bc of the dementia. They cannot follow instruction, remember what they're told, or follow up with daily exercises needed to improve their balance.

My mother lived in AL until her dementia and mobility issues got too bad, and then she went into Memory Care Assisted Living.

My father had a catheter and by the grace of God, I was able to find ONE AL that would accept him. But, they wouldn't care for his catheter except to empty the bag once in awhile. I had to take him to the ER every single time he needed a Cath change or had an issue.

If mother tests for dementia and you have POA, you CAN place her against her wishes if the danger becomes too great. Independence is a facade at 90 when all these health issues exist.

Best of luck making good decisions for mom.
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DrLizGeriatrics Jun 17, 2025
Good points. The one thing I would say is that physical therapy or occupational therapy can be very helpful for someone with dementia.

You won’t teach them the maneuvers to be safer, they will not remember, but you teach their caregivers.

That is why I require every patient to have a written plan of care from PT/OT so all the caregivers can follow it.
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"Stubbornness" is usually the primary symptom when an elder enters dementia. Once others start seeing regular symptoms the elder is most likely already in the moderate phase.

You can't force a resistant adult to do something against their will easily -- even if you are her PoA. Therefore, you can move things along more quickly if you pull out completely and wait for a crisis that will land her in the ER or hospital and from there no one takes her back to her home: talk to the discharge planner to tell them you aren't her legal caregiver and she's resisting care in her home. Then talk to the hospital social worker to see about having her transitioned directly into a facility.

If you keep being The Solution you will do nothing but constantly orbit around her ever increasing needs. If you are not her PoA then this will be very difficult if she doesn't see why she has to pay for anything and you have no power to have her funds cover anything. You are on a track to burnout.

Step away completely and report her to APS. The longer you insert yourself the longer it takes for appropriate care to happen for her.

She probably has dementia. This means she is not able to learn new things. In fact, she is not able to retain what she already knows. She needs a diagnosis to confirm it, but doesn't sound like she'd cooperate. Therefore, step away and report her to APS. It will feel very difficult to do this, but burnout is even worse.
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Please understand that she’s not capable of doing what you ask. She may never be. A concussion is serious, and even more serious in someone of her age.

If she’s not seeing a neurologist, she should. She may need to move to Assisted Living.

I am so sorry that this is happening.
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TannD22 Jun 13, 2025
Thank you. She is very resistant to AL. I’m trying to get support from out of state family, but they don’t realize how serious this is.💚
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I also have a LO past independant living stage but doesn’t want/doesn’t see the need for AL.

No other plan means we are left with *Await a crisis* as the plan.

LO's regular Doctor is aware.
ER Doctor said next admission will start the new journey: ER-hospital-rehab-*not home*-some type of care facility.

ER Dr advised speaking up early to Hospital Social Worker. PT & OT will work on building strength & assistive equipment for a safe discharge where possible. If not, Social Worker helps with next steps for an alternative.

Having a location planned would help smooth things. I reasearched locations, care level & costs for another relative. When a temporary stay had to tranisition to permanent (due to crises) it was difficult but not impossible.

With the next one, I lack any authority to make a start. It will take a crises.

TannD, would you Mother be open to the idea of a Plan B.. a Backup plan?
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TannD22 Jun 14, 2025
Thanks for responding. I have addressed a plan “B” a few times. She is totally against it. We are working on occupational therapy to help her learn new ways to complete necessary tasks without bending over & losing her balance. She just doesn’t stick to it. She is open to the fact that this may be her new normal for a while.
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Maybe she needs to transition to Assisted Living.
At this point..a 90 year old Stubborn person is not going to change. (I kinda know, I'm not 90 but I am stubborn and I wanna do things the way I wanna do them.)
Or you just let her do what she is going to do.
Honestly if it isn't this it will be something else and she WILL fall again.
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As far as I know, you can’t.

My dad (who had dementia and a lot of other issues) had dizziness and saw flashing lights upon standing up (sometimes but not every time) and it led to falls and injuries. He could not or would not comply with medical advice around that including he could not or would not drink anywhere near enough liquids so he was constantly dehydrated which also made him light headed and contributed to kidney failure. Even with an aide sitting right by his side, falls were inevitable when he was living at home on hospice. The last few days, he was at a hospice facility where they put his air mattress all the way on the floor with alarms on it and bolsters on either side. He could not fall while trying to get out of bed because he could not get to a standing position. All he could do was crawl. They put him in a padded wheel chair / lounge chair kind of thing during the day and he was corralled in with barriers so he could not get out of that either without aide assistance. None of those means were possible at home.

good luck.
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Jannycare Jun 17, 2025
Not certain, but what you describe about your dad's issues upon standing and dehydration sounds like "Orthopedic Hypotension". It's when blood pressure falls upon going from laying/sitting to standing position. Few medical professionals catch it because nobody in this world ever takes our blood pressure while standing. Consider having your dad's doc take his BP while sitting, then have him stand up and take it again within about 30 seconds. There are meds that might help this, unless your dad is already being treated for high BP.....which actually cause orthopedic hypotension. It's a vicious cycle but sometimes docs have people on too strong of high BP meds. If your dad's not already on BP meds, then low dose sodium tabs can be prescribed to ease those symptoms upon standing. Also, generally folks who have this infliction often find when they stand up, if they just steady themselves with a cane or walker, and not try to walk....after a few minutes it calms down. Also, another technique is prior to standing up, kick your feet and stomp them a bit while sitting....getting the trapped blood out of them so blood can rise to upper body...brain and heart. Often makes the standing up experience less scary.
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Has she ever had a cognitive or memory test?

Are you her PoA?

She doesn't seem interested, willing or able to do what it takes to keep herself safe in her home. So, if seasoned caregivers here tell you that she won't change and therefore is a danger to herself *and* is overwhelming you with concern and needs... what will you now to do? You're the only one able to change concept of what a solution will look like. She's not going to change and is heading toward the cliff named "Medical Crisis".

If she lands in the you may have the opportunity to transition her directly into a facility at that point, but not if she's still legally making her own decisions. You can try to convince the discharge planner that she's definitely an "unsafe discharge" and she is refusing appropriate levels of care. Talk to a social worker at the hospital.
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TannD22 Jun 15, 2025
She had cognitive testing prior to the fall/concussion. I sent her PCP a referral request for a Neurologist.
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And, since she refuses any help, and doesn’t seem to be aware of all the risks. She needs to be evaluated for dementia. You can remember the date and the president and still not have the risk awareness to be taking care of yourself and making your own decisions.
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It does not sound like Independent living is enough supervison forher well-being.
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