Mom can’t seem to remember that there is help in the other room. Any ideas?

You can't get a dementia patient to stop arguing............never gonna happen. Period. So stop trying. It's a waste of time & energy.

I suggest you have the care givers stay in the same room with your mother. Either that, or have them go into the room she's in every 10 minutes to see to her needs and as a reminder they're still there, and that she's not alone. Have them ask her what she needs, if she's hungry, needs to use the bathroom/have a Depends change, etc. Make sure they're bringing her fresh water and/or beverages as well since the elderly get dehydrated in a NY minute.

If the in-home help does not work out, then it is time to look into Memory Care homes for your mother. It's actually a less expensive alternative to round the clock in home care and also gets you to stop listening to all the arguing and complaining. Plus, she'll get plenty of activities to keep her amused and others to interact with every day, in addition to hot meals & snacks.

Wishing you the very best of luck.

I think it’s the caregivers responsibility to provide care. What the heck are they doing there out of sight of their ward?

They need to have a comfortable place near your mom where they can interact with her so that may be what is missing.

Or maybe mom should have a comfortable spot where the caretakers are and get some relief from being isolated.

It makes no sense to be paying someone who is out of sight, out of mind. Are they not even mindful of your mother’s calls to you? That’s also the point for being there, to enable you to do what you need free of worry about your mom. Instead they’ve created a new point for arguing.

Good luck,

charlotte

I'm a Certified personal care aide working for a good agency for 4yrs and so I've cared for dozens of clients with durations ranging from just one shift to as much as two yrs. You didn't say in your question why the caregiver remains in the next room. I ask because in my experiences I've never situated myself in another room and out of the sight-line of the client. I would think it would be all the more necessary to remain where a client could easily see the caregiver if a client was anxious about being what she perceived to be "alone." The caregivers should be meeting all of her needs for ensuring she has fresh fluids at all times, that she is comfortable including with the temperature, that she is receiving frequent snacks, beverages and meals, that all of her toileting needs are met, her surroundings are clean and neat, that she is safe from falling and other accidents, and that she feels acknowledged and like someone truly cares about her as a person. None of this can happen if a caregiver is camped out in another room.

First..you can not get her to stop arguing about this or anything. Just tell her that they are there to help when you need it.
Second.
Why are the caregivers sitting in another room? If they are supposed to help her they should be with her. If she is sleeping someone should be checking on her every once in a while so when she awakes they can get her up. If she is sitting in her room, they should be checking on her and trying to engage her as much as possible. They should be talking to her, popping in to check on her, encouraging her to come to the kitchen for tea or coffee a bit of a snack.
It sounds like you need to have a talk with the caregivers. Make the house an active one make a bit of noise, run the vacuum, the laundry make sure mom knows they are there.

Have you had her evaluated for dementia? If she has dementia, you will not be able to reason with her.

She actually may be ready for memory care.

We had this with my mom too. She actually ordered the evening/nighttime person out of her room because she said she couldn’t sleep with someone staring at her (or breathing too loudly, or breathing period..you get the picture). So the aide would sit in the other room plus we had a baby monitor so she could listen for any issues, plus she would peek in at predetermined intervals.
that being said, mom would still call-sometimes all night long-help I need help there’s no one here with me.
things we tried:
leaving notes in critical areas (next to phone, in kitchen, etc) reminding her that there are people there she can ask for help. It might be even more helpful to put a sticky note on the phone itself so she sees it before she calls,
we also disconnected the phone next to her bed and “lied” and told her there was a Verizon issue-so she couldn’t call. The aide still had her phone plus the other phones were working just fine.
we also shut our own ringers at night so even if she called it wouldn’t wake us up. Sometimes we would just block her number overnight so the aide and anyone else could still get thru.
begging and pleading and arguing that we all needed our sleep otherwise we could lose our jobs got nowhere-so we had to become more “resourceful”.

If she has cognitive decline or dementia (Which would explain why she can't remember caregivers are there in the house.), then, you won't be able to get her to remember, understand, be aware, etc. of some things. It just won't happen. So, you learn to work with it, tolerate, redirect, manage it day by day. I would examine few things to see if the matter can be helped though.

First, when she calls and says that the caregivers left, is she scared, confused, anxious? Because, sometimes, with dementia, their mind is changing and things can be scary. They need constant support and reassurance that things are okay. So, having someone nearby for comfort can be good. I'd discuss this concern with the caregivers. They should be trained in working with people with dementia. And, they should not be leaving her alone in a room. She could fall, ingest something harmful, get sick, leave the house, etc. So, if they are properly trained, they'd know how to properly supervise and comfort her. I'd put it in writing as to what is expected of them.

I'd also discuss it with her doctor to see if she needs meds for anxiety. My LO took a small dose daily med for anxiety and depression. It helped her worry less.

Sometimes, the complaining about not needing help will pass with time. But, if not, it's just something to be tolerated. I don't know of any way to make a person with dementia get it. Reality is just not something they can handle much of the time and they may never agree that they need help, no matter how dire the situation.

Oh, I'd also make sure that the caregivers are NOT leaving early, like she says. lol

What has helped us with some of that is a large white board with reminders on it. You could put
MOM-if you need anything there is a house helper in the other room, just call out and they will be here. (Or get her a bell to ring)
Your house help people are here to:
1.
2.
3.
(list out their responsibilities)
If you feel ill, let them know and they’ll help you or call me.
if you run out of things tell them and they’ll get a list together for me.

also list upcoming appointments and activities for the day/week.
this helped my FIL a lot. We even have reminders of MIL’s care/condition.

My mom did that "I don't need anyone here in my house" thing. Then when she accepted having help and stopped complaining about it, she would still call me, even while looking straight at the care giver. The final in-home caregiver was special. She would clean and cook for 20 minutes at a time, then sit and talk with my mom for 20 minutes and make sure she had everything she needed, then continue to do chores. 20 minutes at each chore, then back to my mom. She never sat in the other room. It was what I did too on the days I was the care giver and all evenings. My son and grandson as well. She still called me sometimes, but not as much. The notes on doors and by the phone were ignored for the most part, or she would call and ask me to explain the notes. Now in assisted living she doesn't call at all because she's forgotten how to use a phone. Strange to say, but I miss it a little bit. Mostly, though, I have time to finish thoughts and activities without interruptions. I'm afraid to say that this may go on for some time with your mom. Leaving notes, giving her attention, ringing bells, whatever, she will most likely still call you.

If your caregiver usually sits in the same spot, perhaps you could put a mirror so that your mother can see the carer's reflection in the mirror when she is in bed. It may not work, but it could be a cheap option to try.

Mirrors that reflect other rooms or the outside are actually quite helpful in making people feel not so shut in on their own.