My mother is one of the most miserable humans on Earth, and has been for years. Whenever anyone has asked her "How are you doing?", for as far back in my memory as I can reach, I can never remember her saying "I'm fine". Now she's smoked herself to death. She has COPD, CHF, steroid-induced diabetes, a colostomy, osteoporosis, bone spurs in her neck, neuropathy in her limbs, brittle skin that tears at the drop of a hat...the list seems endless. She refuses to get out of bed to try to exercise to keep up any strength, and wants me to do more and more and more for her.
She's in the hospital right now because of a fall last week. She says her knees gave out.
I don't think it's so horrible that I just want this woman to finally have some peace, and yes, honestly, for the rest of us around her to have some as well. The discord and disharmony this narcissist spreads with her always ALWAYS negative attitude takes a toll. She will never change, and her health will only continue to go downhill.
I realize that I don't get to make the decision of when she goes, but I will admit that I do want her to. I think it's the only way she'll finally be "fine".
I hope for your sake she goes first.
this way…. Nobody should suffer even if it is by their own doing, and now you are suffering. My mother has Alzheimer’s, completely out of her mind, stuck in a NH, for who knows how many endless years until her physical body says enough. I cant stand it, and we all deserve the right to check out, if we know the outcome of our illness which will cause suffering for ourselves and others, then a simple legal doc should do it!! This needs to change now! Nationwide!!
It will take time after this slog is over to feel more like yourself again . But yes, it will be a little different than before . Caregiving leaves a mark , at least I feel like that . (((((Hugs))))
She has had many visitors, including her grandson who flew in from cross country and all of her other grandchildren, relatives, friends, church people…she receives cards, letters gifts, food. Yet she makes lists of things to “discuss” with me when I come. It literally amounts to a complaint list.
She is so blessed in so many ways. I have friends who are HHAs and their clients either have no family and friends or have family living very close by who don’t even visit on holidays.
My goal was to make mom’s dying days as pleasant and peaceful as possible. Now I just dread my time there, especially my one overnight shift I do on Saturdays. The next time she pulls out her list I’m going to ask her, who would she like to see, what would she like to do, what does she really want to talk about while she still has time? I feel like all the negativity and focus on minutiae is her way of denying her inevitable death. She’s always been big into denial.
PS. After reading through a lot of this thread, I don’t wish my mother would die. It’s more that I wish I could get some peace and resolution. If she were to die right now I think I would feel very conflicted.
Live and let live.
There are old threads that remain alive because others are in the same situation as the original OP. So, the purpose of the thread is still relevant today. Caregivers have always struggled in the past and continue to struggle today.
It cannot be over fast enough. They are lingering and I want my life back.
Yet, so many people say cruel things to the caregivers and try to make them feel guilty for feelings that are completely normal to experience.
They will say, “You’re going to get old one day!” As if, that helps!
you are so stressed and overwhelmed and you sound like you hit your limit and
your not alone in feeling this way.
I've had those feelings and I’m certain so many others are having feelings like that.
You’re doing your best. Be kind to yourself.
My mother is mean, she triggers my CPTSD, I'm currently not speaking to her and she's staying away. It's been about 5 weeks, maybe more. Yes, I love her, but she will never be the mother anyone deserves.
She accused me of wanting to "take her down". I literally snickered out loud which really set her off. She called me the "C" word. I told her it takes one to know one, and then quickly told her to get the "F" out of my house.
I know she will rear her ugly head at some point, just when I relax just enough and least expect it.
I fairly certain she has found some assistance through the state. She's playing the victim no doubt, how horrible her daughter is! That's okay, when she says those things, she may not realize she's talking about herself.
Just go, I think. Before I do. I need peace. And still want to try and live. I'm unable to stop using (Meth). No one knows and I appear "normal", but it's causing me neurological damage and I need to stop. It's been my way of not feeling. And I do still feel too much, so I fear my feelings and emotions that are justifiable but not appropriate.
Dear God, just let us go.
I will keep all of you in my thoughts. I truly feel your pain. I was a caregiver for my parents and my mother lived in my home for 14 years. There were many days that I thought that it would never end.
Caregiving is the toughest job in the world.
just because we hope for things doesn’t mean they happen .
Caregivers are only human and have feelings .
It’s clear you didn’t have abusive parents. That’s good.
We should all have been that lucky. Some forum members had extremely abusive elderly parents their whole lives. So abusive that you even wish them to die.
It’s also clear that no one in your life has ever treated you SO badly, that it crossed your mind you wish they would die.
Sometimes it’s not possible to understand, unless you lived the abuse yourself.
There aren’t enough words to describe what you are going through. I feel your pain.
It does seem like it will never end while we are going through our stint in caregiving.
I look back on my time in caregiving and wonder how I got through it without totally losing my freaking mind.
Sending many hugs your way today.
I am waiting for something to finally happen and it never does. I really can't take it anymore.
I get it.
Im suppose to read it but haven’t got it on Audible which is the only way I’m ever able to read anything more than golden nuggets messages on these forums. I wish we knew how to age gracefully . Even the most disturbed of us when we get to that point of no return. It might be in those pages.
From tiredsister:
I am reading "Being Mortal" right now.
So far, Dr. Gawande sure knows how to describe our failure to provide real care to our elders (from the elder's perspective) in our caregiving institutions, and explains the evolution of how current practices came to be.
I'm really hoping he will reveal some workable solutions too...some light at the end of this dark tunnel.
My mom is so abusive. I have bare minimum contact.
I wish her to die, because she’s so cruel.
How someone who has smoked 60 years, has PVCs, blood pressure all over the place, and wheezes when she breathes can survive a 6 hour surgery is beyond me.
Meanwhile, my own dr is telling me I need counseling and possibly meds to deal with my stress before it affects my health conditions.
My default is to do the right thing, to follow up on all her medical needs. But man, I really can’t do this another 10 years.
I’ve taken such good care of her, that I’ve prolonged the life of my abuser. I’ve prolonged the number of years I’ve been abused. It’s like extending the life of your torturer.
Today I was in a very cheerful mood. Something good happened to me today.
I then spoke to the caregiver on Zoom video about some changes we need to make, but unfortunately my mom could see me too. My mom could see me smiling from ear to ear. So of course, she increased her insults x 1,000.
I was no longer smiling from ear to ear.
I have also sometimes wished someone to die, because of their appalling behavior.
I know somewhere way down towards the first post I added my 2 cents worth. My MIL is in Hospice care but is flourishing, she could probably graduate out of Hospice Care. Imminent death has passed and she really is OK. The kids are still doing 24/7 shifts rotating through the weeks. DH states that this is the way it will be until she dies. It could be a year, even.
We're heading into month 6 of 24/7 care from her 3 kids. My DH is the middle 'kid'. Everything he does or doesn't do is tainted by her overarching needs.
I have no idea how she got these 3 intelligent people to crawl and squirm for her. It's long since passed 'annoying' and has become "INSANE". No other words for it.
I pray daily that she can die, not in pain and agony, just GO.
Our lives are entwined with hers. I get advice to ignore her, ignore the situation, ignore my DH and his craziness over his mom--but it's affecting me seriously.
I'm BACK into therapy. Taking MORE beta blockers and am looking down the barrel of another cardiac ablation b/c my SVT is back---I think I might die before she does.
EVERYTHING is about her. Making her happy, keeping her comfortable. Making sure she has everything she wants and needs.
She's beyond thrillled b/c she has her 'kids' back home and it's just the way she wants it.
Heartbreaking
(((((((((((((((hugs)))))))))))))))) to all of you
and myself as well.
being ignored and invalidated and abused and then expecting the person you did that to to take care of you?
and we do it anyway.
Why? idk
and Hot, we are now part of the club of daughters who have mom’s with better health than us because of us. Let’s laugh for half a minute about the irony. I hope you a good day.
I get it. You are not alone.
Peace to you.
I know it’s hard. Peace to you too.