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Unfortunately, yes! You are absolutely right about the personality changes and the negativity. It’s really difficult to not take your Moms remarks personally. Limiting your calls is a good way to minimize your frustration. You are doing everything you can and if that means calling 3 times a week, so be it! I know that it is hard not to react to constant negativity, but dementia is dictating her perceptions. It’s not your fault that she is unhappy, it’s more likely the dementia influencing her behavior, not you, but still it’s hard to hear! I was a mental health therapist in a hospital for 30+ years.
The counselors had a saying for such situations. it went like this…

”If you try to make sense of insanity, it will drive YOU crazy!” No matter what, she’s your mom, you want to do the best you can by her! Most mothers want the best for their kids. It’s okay to assume that is what your mom wants, but can’t do anymore. So, you have to take care of you now, and that is very hard to do right now! Just do the best you can and try not to be too hard on yourself or her! Both of you are in a very difficult and new situation. Be gentle with yourself and your mother. You are both doing the best you can under your new circumstances!
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Reply to Jhogan47
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I've been participating on this forum since 2019 and I've never really looked at this particular post (because yes, I'm living the "she's no negative" daily reality). My now 95-yr old Mom (who lives next door to me, single, and I'm an only child) has always been an insecure, somewhat fearful, glass-half-empty person. As dementia and memory loss creeps up on her, she started being weepy in the mornings. Totally out of character for her (a crusty, daughter of Italian immigrants from the Bronx). She asked to be on "something" from her doctor. This is a woman (an RN by profession) who barely took an aspirin in her life. Her primary doctor started her on the lowest dose of Lexapro. It worked really well with no apparent side effects. And, she seems less negative.

I can't stop her from watching "Anger-tainment" fear-driven news all day but I have learned how to blithely redirect our conversations away from mental and emotional and pointless junk. Or, I just pretend my phone is buzzing and excuse myself to "take this phone call".

I just wanted to put a plug in for prescription meds to deal with demented elders' anxiety, agitation and depression. It doesn't work for everyone, or all the time, but it's worth pursuing with their primary care physician so we caregivers don't get ground down to a pulp. Also, our LOs with dementia are losing or have lost the areas of their brain that can bring their minds to a place of peace, contentedness and acceptance. They can't help it and the meds are merciful for them...and us.
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Reply to Geaton777
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I agree Geaton ,

The problem sometimes is getting an elder to take a med for these issues . My mother refused , said “ those are for crazy people , I’m not crazy “. Some ask what every pill is for and in my 2 LO’s experiences , both facilities would not lie to them .

Or like my in laws , “ there is nothing wrong with me , my brain is fine “. It is interesting that they both said the same thing considering they are divorced 35 years and did not communicate with each other . FIL passed Jan 2024.

We just saw MIL this weekend ( lives 4-5 hours away) . Spent all day with her . I’m convinced that my suspicions have been correct that she has dementia as well . Definitely saw the progression from months ago . We did not bring up dementia or her brain at all . We talked to her about driving since she recently had a fender bender . We brought up her reflexes since she is very physically frail as well . She argued the accident wasn’t her fault . She made a right turn at a stop sign. She did not have right of way obviously . Her excuses of why it was not her fault were not rational .

Then she kept repeating that there is nothing wrong with her brain , and that if she thought she could not drive , she wouldn’t . We never brought up her brain , she did . There were other examples , in various conversations , which convinced me she has dementia as well , her reasoning is off . She like my FIL will never agree to cognitive testing . ( FIL was finally tested later , but refused to go to neurology for follow up , and his primary was not willing to list it as a diagnosis . She wanted neurology to do that ). MIL’s memory still appears good .( I did notice some comfabulation) . But I highly doubt a doctor will pick up on anything during a 15 minute visit . She can showtime well , seem normal .
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Reply to waytomisery
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OMGAHHHH! I’m soooooo where you are RIGHT NOW!!! Sorry…I can’t give you a solution or even an opinion, for you’ve asked JUST WHAT I’M WONDERING. Can’t wait to read these comments/replies. I’m with you @jeweltone. I WILL say, I’m praying for you and your mom as I pray for myself and my mom. Blessings & strength.
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Reply to GSUSgirl
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GSUSgirl Oct 7, 2024
I forgot to share that I’m an only child and the difference in us is that my negative, never satisfied mother lives with me!! I recently moved her here about 3 months ago because she lived 12 hours from me. My husband and I went to visit and within 4 months, (since we were last with her) her health and her memory had declined terribly! It has been quite the challenge. All I can say is “thank God for Jesus.”
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I totally understand where you are coming from.
My Mom just stopped walking in 2018 and is stuck in a wheelchair...just like I told her she'd be if she quit walking....now I'm very limited as what I can do with her anymore. I used to take her out to eat, to go get her nails done, etc but now all I can do is take her for fast food or a ride in my car cuz I can't get her out cuz she can't walk. I don't feel sorry for her because I warned her. I told her she gave up on herself and she did and it's not my fault....and it's not your fault either. They lived their lives...it's time for us to live ours.
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