Hey, still dealing with my mother's verbal abusive behavior towards the staff. We are currently trying anti depressients to see if this helps, too early to tell. We have tried them in the past they did nothing, but I am humoring her current facility.
This brings me to the my question, we have found a new facility, thing is they have policy (which I have to look into if it this is legal) where they do not allow overnight stays outside the facility. Outside of that one policy they have good reviews, we toured the place it seems great. They also claim to have experience with difficult residents. As did the other place but it is what it is.
Should I view the request / policy to not take my mom home for the weekends as a red flag?
Have you tried telling mom if she mistreats the staff during the week then no weekend visits?
I only ask because she clearly can control this behavior since she doesn't do it to the other residents.
For many over night stays can be confusing.
Often there can be behavior problems when the resident returns.
For many routine is important and a visit overnight throws off the routine.
There are regulations for each State.
It is possible that the Doctor has to sign off on the visit.
Check "Medicare Bed Hold Policy"
You can view it on line. Might be faster to look through if you Google the Hold Policy for your specific State rather than going through each state.
If the place that allows no weekend visits wants her, let her live there. Allow the professionals to deal with her.
Then you can stop thinking the problem to death and resume normal life.
Cover909
If it doesn’t help her by taking her home, plus the fact that it is going to be against the new facility’s policies, why would you even want to bring her home?
What stage of dementia is she in? I hope that you see some improvement with her meds.
In theory she probably did not "need" to be placed but we also could not afford the 24/7 care required to keep her safe or the people in her building. We placed her after she nearly started a fire that could have burned down her apartment.
We enjoy her company, and she enjoys seeing her family that is why we take her home. We placed her because it was unsafe to keep her home, not because we never wanted her to engage with us.
See if you can find a geriatric behavior specialist to see her. I’m not sure what the goal of an antidepressant actually is, but our behavioral specialist put together a group of small doses of two or three medications that achieved near miracles for my LO.
Still, she was in a very good placement for a little over 6 months before she was able to relax and enjoy her “hotel”.
You should be able to view any policy that they have, but be very certain that she benefits from leaving her “home”. Many residents thrive on aand if she does, she’s entitled to it.
Might be time to let the trained people handle her and not keep running the same tape over & over in your head and accomplishing nothing.
She is a manipulator, has the routine down pat, gets you all worked up, keeps the stress level high. Works for her, what about everyone else?
Cover909
My LO was taught to be 'good in company'. This is deep seated & she shows respect to any staff/ care workers. But out of their view, with family.. she can become bossy & attempts to control us.
Your Mom is sort of the opposite. Pleasant to you & other residents but reacts with rudeness to people in 'authority positions'. Has she always been like that?
I hope the next month brings positive change.
I swear when she hears people say we can handle it. In her head she is like hold my beer, and takes it as a personal challenge.
If your Mom is in a Memory Care unit, routine is extremely important so I totally agree with the policy of no overnights, unless you are taking her on the very rare vacation multiple day vacation.
If the new facility is used to dealing with difficult individuals, the reason for no overnights is because sometimes, what is needed is "structure" and routine. My Mom is in MC. When she was in the hospital after oral surgery, she insisted on waiting in the hall so that she could get a bath. They couldn't get through to her that she was in a hospital, so after 30 minutes, they finally restrained her to the bed (yes, she tried to bite them and punch them) and sedated her. (...and that experience is a different topic.)
So I totally understand the "not take the person outside for overnight trips"
I would ask the facility for clarification, Exactly what time of the day is she expected to be at the facility? Can you take her out for an extended vacation? If your Mom is not going to MC, does the rule still apply to her? Why did they put the policy in place?
As for you, I would reflect on your Mom's behavior. Could the fact that you are taking her overnight be the reason why she is abusive to the staff?
Just a few thoughts....Good luck!
In an ideal world she would be home with in home support, but medicaid will not cover that. They do cover SNF care especially if the home is not a safe discharge.
It appears to be a MC only policy. They mention it is for the my mother's benefit and the residents. Seeing people come and go can be stressful for other residents.
In case of my mom I understand I the future she may become combative and forget where she is. As she stands now she is not like that. She still remembers us, and we want to have her enjoy her life the best she can before the disease robs her of everything else. We not trying to speed it up.
I have thought about that. Say that is the case what exactly does that mean? Leave her in the place do not take her out have her feel alone and isolated pray and hope she adjusts, and if she does not adjust leave and let the staff do what is nesscary to clam her down?
Potentially turning name calling into something more primal or violent?
I am sorry I am just a tad stressed, all this hassle over what largely amounts to name calling is insane. I have asked many times it is gets physical and they have said no.
Each time my mom came back to her NH from a hospital stay, they did an intake with her, which included preference both baths or showers. Also what time of day they got her up and prepared her for bed.
These are basic human rights; they are spelled out in detail in "the NH Bill of Rights" posted on the lobby of each facility.
And yes, this was a NH that accepted Medicaid.
Good Nursing Homes exist. Persist in your search and ask about the reason for policies. Call the Ombudsman if you want to know if the patient's right are being violated.
Maybe seeing less of her family will help her adjust overtime, or possibly foster a new family or comfort zone in the facility. Hard to say, but taking someone out of MC every weekend seems cruel you are robbing them of the chance to find solace and find peace in their new home. If you keep reminding her she has a home elsewhere and family outside the place she spends most her time what good does that do for her?
You placed her because you must have known you could not take care of her anymore. Let professionals do it, give up the control let them take over. You are clearly a control freak, and I get it that is your mom. Problem is if you want absolute control take her back home and care for her. Don’t make the job harder for those doing the actual care giving on a day to day bases. Her behavior may be cute or funny to you, but it is damaging to caregivers that work in these facilities.
Take a hint, your mother sounds like a handful, you’re doing all this fighting only will make it harder for you to find a place for her. You need to learn to play ball with placement.
If you move your mother to the new facility, you won't be putting her into "care". You'll be putting her in prison. My friend, there's no need for such cruelty. This is coming from me and everyone here knows what kind of relationship I have with my mother. Even I wouldn't place her somewhere she wasn't allowed to take a few days off from.
So in plain language, don't do that to your mother because it's wrong.
Since you don't mention dementia, I'm going to assume that your mother is mentally capable rational discussion and can be reasoned with. More likely than not, you've got a senior brat on your hands and "meds" can't fix that.
So you, your mom, and and the administrator of the facility she's currently in should have a sit-down. Tell her plainly that either she cleans up her abusive act where she is, or she will be drugged with anti-depressants and then moved to a different facility where she will not be allowed to leave for a weekend, and in turn will be spending every night for the rest of her life there.
I think she'll clean up her abusive behavior and start being very cooperative with you and the staff.
I don't know if you're aware of this or not, but if your mother does not have dementia or has not been determined to be mentally incompetent, you nor anyone else has a right to push any "meds" on her without her consent. So, I hope for your sake and the facility she's in that she doesn't make a call to her doctor and say something.
Have the sit-down with your mom and the facility administrator and see if she can stay. Tell her what I told you. If her behavior improves forget about the psych "meds" and give her a chance. If it doesn't, move her out (make sure she's declared incompetent first) and drug her if that's the only way staff can deal with her.
She does have dementia, and she is currently in a MC of a SNF because she was denied home care hours but she also nearly started a fire in her apartment so she was unsafe, and we could not be around 24/7.
We have tried to explain it to her, even prior to dementia my mom has always been a stubborn and difficult person to be around the best of times. Love her to pieces though.
My husband’s grandmother had dementia and was in MC. Her daughter (my MIL) would take her out for lunch on weekends, or just drive around. It was okay for awhile but soon it was a detriment.
She thought they’d been out of town and worried that “the hotel” wouldn’t let her back inside. Or thought they were moving away. Once she got back, she couldn’t find her bathroom, wasn’t sure where she was. It would take 24 hours at least to re-orient. An outing that was a few hours to us was a week in her mind.
Eventually my MIL realized taking her mother out was something of a selfish act. It was making MIL feel better about having to put her mother in MC. But it wasn’t helping her mother at all. From then on, lunches and visits were brought to her.
The vibe at the facility is eh, we are relatively loud and bombastic people, we have parties all the time during the summer. My mom loves this she lights up being around family.
I get it though I have to think long term. Just seems cruel to speed up the time line.
I would keep searching for a better place.
Are there Board and Care facilities in your area?
Is there any staff training around dementia for the staff? Watching a couple of Teepa Snow videos and having a facilitated discussion with the social worker might make a huge difference.
Are you in the habit of regularly bring treats to the staff?
I will look into Board and Care facilities. I assume they are more akin to group homes by the name alone. First time I have heard of them.
Unfortunately each place came highly recommended for as dementia specialist.
I use to bring snacks and stuff at the start regularly. Then the complaints and death glares started. More and more I felt unwelcomed. I am sure my mom felt the same.
More and more it sounds like there is something else going on here besides dementia.
That has been a working theory her doctors have had, but without prior documented baselines and assessments it is difficult to determine now post dementia.
Also as family many behaviors many thought were out there we just passed as old country shit lol.
I keep thinking about Barb saying that her mother grabbed the steering wheel when her husband was driving. They never took her out again after having that experience.
https://www.agingcare.com/questions/wife-alzheimers-home-from-facility-for-weekend-155988.htm?orderby=recent
Hay Look you used live somewhere else... but not here...
too bad... You LIVE HERE....
OOPS, my bad (bad grammar) you cannot stay here... it's just a visit to somewhere you want to stay...but you cannot.... oops... sorry... bad humor... bad choice... either way... It's not good.... cuz you cannot and will not reside here... oops... I forget we have ALZ ...... my dementia,,,,, thinking I could show you where you used to live... but in reality.... you cannot... because.... it's not safe... and because..... we don't have enough......(fill in the blanks if necessary ).
FOR MOM'S SAKE..... DO NOT TEASE HER BRAIN... THAT IS MESSED UP IN SO MANY WAYS.... THINK..... AND THINK AGAIN.... HAY... LET's PLAY.... MESS WITH MOM'S BRAINS.... BRING HER HOME FOR A NIGHT.... PRETEND... AND TAKE HER BACK AGAIN...BECAUSE I cannot stay... got work the next day.. Mom needs 24/7 care.
I TRIED... and some many people here actually do this and succeed!!! CAN YOU BELIEVE THAT? MANY PEOPLE DO THIS, LITERALLY.... and it works... !
All I know, I tried.... And I didn't last that long... hubby called me out on it. He realized I was not sleeping.... at all...I still feel guilty...
I understand one day it may be too much, and I will have to adjust when that day comes. This disease will eventually take everything from her, if she still visibly enjoys her weekend trips with family I do not see the harm in that. Why take away something she enjoys before i have to.
I will stand firm, be the best advocate I can for my mom while making her she enjoys life as much as she can given her situation. I will still be looking for a facility and my primary goal will be to my mother not to nesscaryly make the lives or jobs of the staff easier.