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It's not honesty, it's the dementia talking. I know, this is easier said than it is to accept. When you get tired of the criticizing, get those silicon earplugs.

Clean your home according to what works for you. I had a client that did that ongoing criticizing and was mean and nasty all of the time. I don't know what to tell you about letting this roll off your back because I'm not good at this either. I spent all day running around trying to please this person, and the more I did the more she demanded. It became so bad that she would chase out her weekend help and would leave the weekend chores for me to do from the other home health aide that did not get completed. Of course, it was the aide's fault. No, she would bully and chase the nurses away.

One particular bad day, she was on my case all day. I went downstairs to check the laundry and just sat while the dryer was going. I could hear her upstairs complaining and getting meaner by the second. When it was time for me to leave, she blocked me from getting past her. I was standing on the steps to her basement. She kept turning the lights out in the basement. Then I had to listen to her speech saying that I was there primarily for her needs, she is paying my salary, I need to do what I'm told and so on. Then she proceeded to tell me she didn't trust me, and I'm stealing her supplies. I don't know what happened, but after not eating for six hours with the exception of a cold piece of chicken and a half bottle of sparkling water, enough was enough. I turned around looked at her and told her to have a good life. I had a doctor's appointment that following week and my blood pressure was so high that my doctor was afraid that I was going to pass out at the office. My doctor thought that I had been on a binge. LOL I don't drink due to meds. I don't even have the luxury of a glass of wine with a meal any longer. So no, working this case was putting additional stress on me.
Try to find some quiet time to yourself. Try to avoid, "FOG," (fear, obligation, and guilt.) Start finding outlets for yourself even if it is hiding out in a corner of the basement and sipping a cup of tea, coffee while listening to your IPOD to drown out the complaining. If she starts complaining tell her you didn't hear her since you were busy with laundry. I know fibbing right? There is a such thing as therapeutic fibbing. LOL I would use this tactic to my advantage.
Dealing with someone suffering with dementia means drawing a balance in your life. Exercise helps with stress. I'm sorry this is happening to you, and I hope that she gets placed soon.
Next time mum starts complaining and mean mouthing, just keep upfront that her brain is broken. And this too shall pass.
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This is a mental disorder. She can not control it..My brother is the light of moms life. She has Lewy. When she is even mildly into a Lewy episode he is her “obvious” favorite. She told him I steal her money {I am POA}, I had her locked up, and told him I wrote a horrible letter saying I hate the family along with all kinds of crazy untrue sentences…at first my feelings were hurt badly..I am the care giver…the worker bee. It is so obvious she prefers his company.. I sought counseling to learn to emotionally detach..to recognize that this is her problem not mine..I can not change her or her behaviors. I do my best. I only visit 3x a week , on a schedule …it is about 15 hrs a week.. This is not truly my mom but a body that looks like her. It remains a tough job but I am happier now that I learned I am not responsible to make her happy. Good Luck.
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I have a wife with Alzheimer’s and she exhibits the same traits. Her personality has changed and like your mother Sheffield expects everything done for her . I have someone come in for 5 hours a day to take her off my hands. That’s a necessity for my sanity. I love it when people say it gets worse “ thanks a lot”. Stay strong and get some relief even a senior card “ day care”. It’s needed for your sanity.
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Much of what people say when they have dementia is designed to wound and not usually that valid. It should not be taken to heart.
I once asked a professional why the delusional stuff was always unpleasant - he said he didn't know but it came with the territory.
Many of our parents do have preferred children and do not do well covering that up. My mother was the same - one thing is noticeable though. They are often the absent/less available offspring! 🤔
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You have now found out what she always felt about you! Ouch! But you always really knew it. It’s not going to get any better. Do not sentence yourself to more of this. Take it from me it’s not worth it. Get her in a facility and get in with your life. X
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cherokeegrrl54 Jan 2022
I agree 100%!!!!!’don’t know if anyone has mentioned the Teepa Snow videos on you tube but she’s considered an expert on dementia behaviors. Also Google FOG(fear, obligation, guilt). I WOULD NOT put up with the physical abuse. Call 911 and tell them you have a demented elder who is out of control and she needs to go to ER for eval and treatment. Maybe thanksgiving step will start the process of her being placed in a memory care or AL unit. You do not need this in your life. Blessings to you as you walk this path. What would she do if she’s in the middle of a tirade and you got your purse and walked out, even for a short while and say nothing to her? Also, search for a technique called “Grey Rock”….,,,Liz
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This is sooo hard. So sorry your mom is in her mean phase of dementia. It's brutal, no doubt.

I suggest you come to terms with the fact that it's not going to improve. That she can't properly control her thoughts and what comes out of her mouth. That it's the dementia talking. And that you can therefore IGNORE everything she says. Do not let her snide comments get under your skin and hurt you. Let them bounce off. Just say, in your head "whatever!".

Do you have any timeframe for when she might get into a facility? If it's soonish, just try to distance yourself emotionally. If it's any length of time (like more than a week or two!), start hiring some help with her money to take care of you. She won't like it and will say mean things but what else is new? As long as she is being safely taken care of, she doesn't have to like it. But you deserve a break.
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Cappuccino42 Jan 2022
It’s still months away due to waitlist but also because we are needing to take legal route for POA. She never did the paperwork... as she was stubborn and insisted it would automatically be me, even in the early days. It’s international so a bit more complex. Possible also why she thought it would automatically be me because in her home country it is automatically first offered to offspring, only if they reject does it go to government. Whereas, here it’s the opposite. Sigh.
The only help I’m getting is 1-2h a fortnight that someone comes and takes her out. I haven’t been offered anything else.... unless I were to pay privately which is quite hefty.
ill be honest and say I actually feel pretty disappointed at the level of support available. I feel like I’m just given the run around.
I also asked about cleaning support (just her areas) and was told because she lives with me, it’s considered my duty. Then they agreed that they might just do her bedroom and bathroom. Then that turned to, we don’t carry the vacuum down stairs (it’s a handstick vacuum) and you would need to ensure any clutter is first removed and we don’t move any chairs etc. Well with mums dementia clutter is the problem, ie she puts her clothes wherever and she does have a small desk and chair in her room. The showering help also said, they would only shower if she willingly went in (They wouldn’t try and even pursued her) and there’d be NO heating the room due to staff OH&S. Well, I can say right now Mum would refuse if the room wasn’t warm! I just feel like these services really aren’t catered for dementia.
even the 1-2h outing,. It’ll take half hour before Mum is even in a car! And last time I spoke to them they said the previous outing just over 2h was too long and they’ll aim for just 1h.
I just don’t get it!!
will they be like this at the memory care / aged care too? Will they leave Mum unshowered, in wet depends etc,... because I can tell you now, she needs a firm grip with matters, someone who takes control of a situation.
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My mom was in the No Filter Stage for quite awhile. It was really difficult.

That stage has come and gone.

Now, her language skills have taken a nosedive.

I want you to know that this phase won’t last forever.

I also read your reply that says that your mom is on a waitlist for a facility. Then, you can just go back to being a daughter, and can leave if your mom gets abusive.

May God give you strength til then.
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I'm so sorry for how demon dementia is causing your mom to hurt you, That's how you have to look at it. When son was using drugs and saying incredibly nasty things to me the only way I could cope emotionally was to remind myself that it was the drugs talking.

My aunt will be 100 yrs old in March and has mod/adv dementia. I grew up with my mom, her and her sister, my other aunt (102 yrs old now). Aunt N went through a phase a few years ago where, whenever I'd enter the room, she'd loudly exclaim, "Wow you've gotten fat! Why are you so fat?!" then she'd cackle and shake her head in disgust and disbelief -- and it didn't matter who else was in the room or if we were in public. She herself was always model-thin and proud of it. Nowadays she still spews horrible stuff to everyone but has stopped making the fat comment to me, or any other negative comment. So, dementia is taking your mom into a phase, but no one can tell you how long it will last. All we can tell you is bravo for doing what you're doing and for enduring what you're enduring and just a gentle reminder that you are in no way obligated to do it and that YOU are the priority so please do what it takes to take care of YOU. May you receive wisdom, strength, inner peace and many blessings!
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This has to stop. Mom needs a facility. Yeah she might hate you for it, but she’ll hate you no matter what you do. She is out of control and this is more than you can handle.
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I agree with Glad it is time to start looking at facilities to get her placed. Her behaviors are going to get worse not better.

Your cat is already stressed to the max thus the reason for peeing on the sofa.

You are stressed trying to please your mother and get her to see you are a worthwhile daughter who deserved to be loved the way she loved your older brother.

Your mother is who she always was magnified 100 times more by the dementia. Now she can't hide and pretend like she used to. What a shame that she has such a precious gift of you as her daughter that she could never fully appreciate because she played favorites.

For your own mental well being and financial well being please consider starting to make the arrangements to place her. I hate to see you waste your life and then a few more years down the road having to put her in a facility anyway. With the end result being her cruel words tearing you down so much you never go back to who you were before you became her caregiver.
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Cappuccino42 Jan 2022
Thank you for your kind words. The cats are definitely stressed out and the one in particular doesn’t want to be near her. They don’t trust her. It’s funny how animals can sense that!

Mum is on waitlist for care facility. I just worry how her antics will go there. But also we are trying to sort out her POA prior,.. as she never did the paperwork. Despite all the above, she still wants me as her POA as she knows I’m good to her and because she is dual citizen and I speak the language.

I’m afraid this has all already affected my self esteem. I’ve noticed myself retracting in confidence. I’ve found myself questioning,. Who am I to apply for this or that role when opportunities have been mentioned.
At the moment my workplace is providing me with flexibility care wise but lately I’ve been feeling unworthy and dumb and almost as if others see me like that. Part of this is probably because I’m averaging 5h sleep.

My doctor has referred me to a psychologist but again I’m on a waitlist (due to extreme demand) and it’s proving difficult to find the time between the work I do and the care I provide for Mum.

I’ve attempted to reconnect with my dad (overseas). After all, my mum refers to me often with his family surname. “The,....”.

He never gave up on me, it was just my Mum had custody and moved overseas. We are almost strangers but perhaps I’ll find a connection I never knew existed. I was his only child. Strange how I’m seeking this now and almost feeling guilty.
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Looking for validation, or gratitude, or reason from someone with dementia is the path to insanity.

Please get out of this situation. It's not just your mom who counts.
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This is the way some of them are. There is no changing them. Get her into a facility and go back to your career.
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