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My mother has multi infarct dementia, egpa, liver cirrhosis and copd, and isnt terribly aware of her state or her other disorders that require care. She hates the facility though and keeps trying to escape. Shes hits staff, tried to run them over with her walker then forgets shes done this. She calls the police to get them to take her home. Every other time I talk to her she repeats I hate you, im ashamed of you, and Im cutting you out of my will and your a terrible human being for making me a prisoner. She has cluster b personality disorder(s) which have been exacerbated. I keep trying to impress on her this is a nice place she has her own apartment and the only other option is a locked memory care unit or geri-psych unit which wont be as nice. I tell her i can bring her whatever she needs and the staff will take out to lunch with friends or to a bookstore and they have outings as well she wont go on or talk to anyone on the floor. We put up her pictures to make her feel at home but she just took them all down and piled them by the door because she’s leaving. She’s making herself miserable. Shes pushed the people she knows away and many arent taking her calls anymore because she tries to manipulate everyone into taking her home or screams at them. I try to empathize with her that it must be hard missing home and I also try to distract her which works for maybe thirty seconds and I absolutely hate seeing her like this and was wondering if anyone had any tricks to improving attitude when a dementia patient is stuck on a negative loop. What might help her settle in?

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It is truly an exercise in futility to argue with dementia. Stir in a few spices as in disorders and you have truly a nasty little mix. Ignore it. Visit infrequently and do not speak on the phone at all ever; in fact it is likely best that phones are now removed. If not you simply reply to complaints with "I am so sorry Mom. Love you. We will talk tomorrow". THAT IS IT.
There's nothing you an convince her about. A nice room? Nope. I don't think so.
I would watch a whole lot of Teepa Snow Videos to get an idea how to attempt to communicate best with the very demented.
You aren't responsible for happiness, and in fact, happiness for her is now a thing of the past. It won't return. And peace will come only with death. Those are the difficult truths.

Stop thinking of this in terms of "normal life". That is done where she is concerned. I am so very sorry. It is difficult to stand witness to.
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It isn't anything you can do with a personality disordered case with dementia layered on top of it.

Most of us who grew up with dysfunctional parents learned early on how to be people pleasers to keep the peace.

My reaction to adult tantrums and threats is to ignore them. When she starts on her tirades, hang up. As a nurse told me once when I was on a case, don't accept disrespect.

Realize your mother is in a safe place getting three hots and a cot. If she is hitting and abusing staff, the next step would be a psych ward for medications to calm down this behavior. What more can you ask for. She had round the clock service with aides and other professionals. There is nothing you can do to make things better for her. Sorry to tell you, this is good as it gets for her.

I've reached a point that I can keep a person comfortable in bed and provide care to a certain extent, but when the abuse starts, I'm out. I'm not going to stick around to be slapped, bitten or kicked. This is when I detach emotionally and just make sure this person is not going to harm themselves, and I refuse to let them harm me in the process.
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Your mother is terminally ill with cirrhosis. No meds are going to cure it, only a liver transplant does that, and I'm sure she's not a candidate. That said, mom needs a hospice evaluation where she will be given calming medications not normally prescribed outside of hospice. If you want her to stay in managed care, her behavior must be brought to a manageable level where she's not making others miserable or trying to elope. I'd have her in Memory Care Assisted Living personally, with hospice on board, and meds to control her outbursts. For her sake and everyone else's. Sometimes there's no great answer, especially where dementia is concerned, so we take the least of the bad choices available.

Best of luck to you.
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I didn't read what others said, so this may be repetitive.

There comes a time in are aging parents life that we just have to let go, or it will destroy are mental and physical health, we will ruin are healthy relationships, friends, job , the list goes on...

This sounds to me like , it's time, past time to do that. When your talking to mom , your not talking to the mom that raised you your talking to a very sick person.

There really is nothing more you can do for her. On top of the dementia, the liver and all the health issues cause more brain issues on top of it.

I feel your pain, unlike your mom my mom is aging at home, to make a long story short , I have no control, brother has it all. I visited yesterday and moms cold, her body can't control the heat anymore. She has the heat on 68, because that's where my brother wants it. My brother will have a fit if she turns the heat up.

So should when I leave feel sad,depressed have debilitating anxiety? I have no control, mom won't care what I say only what my brother says. So I can't bring this home and let it distory me. I have to move on, I have to make my own life, no matter how much it hurts, and stuff that inside me.

I have no control, which at this point you do not either.

Read the serenity prayer, a person of faith or not, that pray says it all.

There is very little you can do to help mom right now, and keep your sanity at the same time.

Very sorry for this
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southernwave Oct 30, 2024
Get your mom a heated vest from Amazon (or an electric blanket).

I’m going to agree with your brother on this one. I’m on meds that make me hot and so I can’t go visit my MIL because she keeps her house on 75. Her house, her rules, but when I go over there If feel like I will throw up because it’s so hot.
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She won’t be there long if she keeps assaulting staff. She needs psych drugs that will make assault impossible.
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Memory50 Oct 29, 2024
Yeah it’s a disaster. Shes had police called on her while she was in the hospital for the last two years. Shes always had a sharp tongue but she’s never been physical with anyone. Shes about 80/90 pounds so I think people are a little more lenient with her than they necessarily should be. Its like all the social niceties that kept her in check are just gone. She was a pistol in her regular life but now shes a bit of a menace. Though doubt theyll put her on any other drugs
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How long has it been since she was transitioned into the facility? Often it is suggested by admins to not visit or even call for about 2 weeks so that they can get acclimated.

If she's not on meds for her agitation/anxiety, why not? Even if she refuses to take them she can be held in a psych wing until she does. My cousin was held for about a month and then she finally relented. It is merciful to get meds into her. She can no longer bring her own self to a mental/emotional state of acceptance, so the meds are necessary.

I also wonder why she still has a phone? She's only using it to cause chaos. Take it away, at least until she calms down.

Dementia robs people of their reasoning and logic skills, so it is pointless to try to convince or impress anything upon her — you will wear yourself out trying. Dementia also robs people of their ability to empathize with others. Time and meds is what most likely will help her settle in.
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Memory50 Oct 29, 2024
Her conditions are pretty severe, EGPA is an extremely rare autoimmune disease and basically all her organs are compromised to some degree. Because of this she is on a TON of medication. It takes her a good chunk of the day to get it all down and it really is just awful for her. So basically her doctors want to cut any med thats not absolutely vital. Theres a bunch of stuff she could be on that might help her but they really had to choose which were the most important for her. Because of her cirrhosis the medication doesn’t process that well to begin with. Luckily she managed to input the wrong passcode into her phone too many times so its locked but she still has access to the facility’s. Though I think I might be the one left answering her calls because i don’t want her to feel lonely even if shes just going to throw verbal abuse. All I can do is tell her I love her and hope on some level she hears it. She’s been at this facility a couple months but had two years mostly in hospital or living at home with aids she apparently was also verbally cruel to and kept firing, one because she suspected she stole some cheese. My brother is now POA and guardian and does all the work with getting her set up places, getting her a social worker and has been really great about all that stuff but hes no longer answering calls unless he feels they might go alright due to the verbal abuse shes been giving him, so I do worry she has no one to vent to. This place is much better than the hospital room she just left,
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@Memory50 - what I wanted to say to you is rather long and detailed - having a similar experience with a FIL with dementia and NPD. So I sent you a private message.

If you click on your initials in the top right corner and click Profile, it will take you to your messages.

Long and short - there is little you can do to help her settle. Cluster B personality disorders almost always exacerbate dementia.

Best of luck - and I'm happy to chat in messages if you like.
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Reply to BlueEyedGirl94
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While well intentioned, 'we put up her pictures to make her feel at home ..." - no this isn't going to work with all the variables / mental-cognitive issues you outline.

* Once you understand that you cannot appease her ... nothing will ... you can start to - not only - make decisions in her best interest, but in your best interest, too. .

* While empathizing is understandable, she is 'beyond' you empathizing in terms of directly addressing her "see what I am doing / done for you ... to feel more at home here?" when she is cognitively UNABLE to process this and changes that have been made and need to be made. She is FRIGHTENED, MAD/ANGRY (I don't need to tell you that), and she doesn't know what is happening nor what will happen.

* You need to take control of the situation in understanding her limitations due to her having lost brain functioning/brain cells. She is doing what she can - scream / express her fear and confusion.

* Consider medication; talk to the facility medical staff / administrator.

* The best one can do in these situations is 'self-protect' (do not take her behavior personally as it isn't (I know... not easy to do). As you can, let her rant to 'get it out' and then leave when you need to, saying "I am going to talk to the Director here and see what I can do for you." She may or may not get that, but saying it may get through ... although DO be aware of what is important:
- make eye contact
- hold her hand for reassurance (if you can)
- talk with a quiet / even tone of voice
+ These non-verbal behaviors will get through. And, the key is often non-verbal communication / interactions that make a difference to her (she feels safer, more ease due to feeling more relaxed [possibly] ) - verbal communication won't do it.

Yes, you 'hate seeing her like this.' This is understandable. However, the trick to improving attitude - is actually changing your attitude, not hers. The 'trick' part, which isn't a trick is mentioned above in how you communicate with her (eye contact, calm voice, reassurance --- and MEDICATION management.)

Yes, there is a negative loop - the brain 'does that' to the best of us with full brain capacity. (Read Rick Hanson's Buddha Brain). Check out TEEPA SNOW - her website, webinars, books, You Tubes. She is one of the country's best experts in dementia and how to work with / support people where they are.

And lastly, take care of yourself. Meditate, take walks in nature or knit - whatever relaxes you and shifts your feelings - mindset. This is a very difficult, heart wrenching situation. Be kind to yourself realizing you are doing your best to figure it all out. Often, for the best of us ... working with this population (i.e. dementia) in this field are perplexed and have to figure how communication and the best way to proceed ... the way I ... have proceeded is with educating myself with how the brain changes, knowing what I can do and can't do, developing compassion, not arguing or trying to convince (it doesn't work; they cannot comprehend due to the lack of brain cells / brain functioning). What a person with dementia GETS is ... kindness through actions as presented above. Be present with her as you can. Perhaps try massage / gentle touch. Stop 'thinking' you can talk to her to change her - you cannot. Educating yourself on dementia will help you learn how best to proceed / interact with her.

And, do know you are grieving a major loss, even while she is still here. Get therapy / counseling / support as you can / need to - to get your feelings out. Honor how you feel. It is a major loss. And, you do not want to see your mother like this - it hurts. She hurts. "If" it might help her, get volunteers or caregivers in to be with her.

Gena / Touch Matters
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Your Mom should be in a Memory Care. Your brother should take her phone away and she should not be allowed to use the facility phone at all. Maybe you can get an Alexa where you can drop in to see how she is doing. Calling 911 is very serious.

Is Mom considered terminal? Are these meds just prolonging the inevitable? If so, why not get Hospice involved. All the life sustaining meds will be stopped. Only those for comfort will remain. No more doctors or poking and prodding.
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Memory50 Oct 30, 2024
She is in hospice. They aren’t try to cure anything just make her comfortable and all those medications are required for that.
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Put her in a locked memory care ward for her own good, and stop being so available to her. It’s only a matter of time before the facility she is in kicks her out.

Why are you disregarding her cluster B mental illnesses?
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Memory50 Oct 30, 2024
Not disregarding her personality disorders but they are personality disorders and every therapist she’s had have only been able to help her manage them so much. They kind of are what they are.
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