Guilty thoughts about wanting it to end??

I’ve only been in serious caregiving for a year and mild caregiving for 2 before that. I am amazed at those that have done this for years and not gone crazy themselves. I think 2 factors must help some. You must have a good loving/liking relationship for the one you are caring for and the person receiving the care must have at least had that loving/liking relationship before or during the caregiving.
I love my dad but have strived to not be like him since I was a child. He was abusive, alcoholic, negative, mostly absent, depressed, living in regret, living in the past, and tried to manipulate others into loving him. Also after my parents divorce he became a hermit and lived alone with very few relationships outside of immediate family. His closest friends in the last 15 years has been doctors and pharmacists. So for me not having the like factor and add onto it the strain on my personal life, marriage, career, finances, social life, and mental health; I really want the dementia to progress faster and force residential care and hopefully a short time until death. He consistently says he will go shoot himself in the head if I try to put him in a nursing home. But I know I can’t continue to care for him in my home without loosing my wife, job, and house.

No. You are not alone. I feel like not being on the planet if this is the rest if my life...like it will never end and if it does I fear I will be so old and screwed up that it wasn't worth living anyway.
Hugs

I wish my mother dies every day after nearly 6 years of looking after her with no family or friends to help. Maybe I will burn in hell but I feel like I am now. You are not alone in your thoughts.

Are you a horrible person for your thoughts?

If you are, then everyone who takes the role of caregiver for a loved one is a horrible person. The person we take care of is not our parent or our spouse, it is someone we never met who never did anything for us, but we are obligated to take their abuse.

"There are times I just wish she would pass away so I could regain my own sanity." I think we have all had these thoughts or desires. I think you are perfectly normal. I also believe you and everyone else who takes on the caregiving role deserve a hearty round of applause from other family members. Well done!

My wife's first anniversary in long term care is next week. Before she went into the facility, I was constantly reminded that the only way the situation was going to change was if one of us died. After she called the police on me I realized the situation was beyond my control.

When I meet others in our situation, I remind them that the most valuable asset the sick person has is their caregiver. You need to take care of that asset. Without you, the sick person is even worse off.

Oh, one more thing, they are not lashing out at you per se. They are lashing out at whoever is taking care of them. They are mad at the disease, but they are taking it out on you.

No, in my case it is my mother-in-law. My husband can only be around his mother for about an hour a week. I am there all weekend with her to save money on care and sometimes I want to throw her thru the window. You are not alone.

I am in a different boat. My mother is 88 and still lives on her own. She can do most things for herself. I am only her transportation and I make and take her to all her doctors appointments and with Covid have been doing the marketing for her. She is a wonderful person and has always been a wonderful mother, but I am 67 years old… Not old, but no spring chicken and I have some issues with health and so does my husband. Here’s the thing. In the past there was only usually one senior generation alive at a time. My mother’s parents passed when she was in her 40s. Now we have the boomers and the parents of the boomers alive at the same time. It makes it very difficult for people who are already entering their senior years to have to be responsible for people who are even more senior. My mother never had to deal with that. I love my mother dearly and will be in a zillion pieces when she is gone, but being a senior responsible for a senior is difficult. I worry every day about when the next shoe will drop and she will not be able to live on her own. It’s the worry for me not as much the actual caregiving… Just the never ending worry about what comes next.

I am in the same boat. You are not alone. You are not a horrible person.
There are days when I look in the mirror and I don't even recognize the person staring back at me. There are also days when I am so angry and so resentful I am immobilized. And, don't even get me started on the family members that don't do a thing to help. Nothing at all. They are the people who should feel horrible and they are the people who should be ashamed of themselves.

There are no "right" answers for you except don't give up. Reach out as much as possible. Get some rest. Try and Let Go as much as you can. I have started shifting my thinking a little and the smallest change has made a huge difference for me. For instance, when I am asked to get something rather than jump up no matter what I'm doing I say ok, wait I'll get it in a minute. Just something that small has helped my stress level. Try to start making tiny steps to help yourself.

A few times a day stop, take 10 deep breathes. It helps a lot too.

My heart goes out to you.

But, I must strongly disagree with those who say every caregiver feels this at one point or other. That is not true and, in my personal and professional opinion, this attitude/belief/experience should not be normalized as the expected experience of a caregiver.

One way or another, caregiving is a choice. When a caregiver accepts this role, it is their duty to ensure their loved one is safe, secure, and as healthy as possible. It is also the duty of the caregiver to care for themselves so that they do not sit around wishing their loved one is dead - that is simply not fulfilling the responsibility of safe, secure, and as healthy as possible.

It is critical that you find support:
A group to give you tips, tricks, and resources. In person or online meetings are available to meet you where you are with a variety of options.

An outlet for your mental and physical health. Exercise and meditation are the minimum of wellness care and you can practice them in your home with a computer, or find locations outside the home. Move up from there as needed.

Respite care - even short-term respite - for you to step away from your loved one seems to be in order at this point. You need to think outside the box to ask for help - those resources you find in a group will help, and the investment in your physical and emotional health will help you make the most of the respite care you can put together.

Finally, it is OK to stop your role as a caregiver all together. That can be done more easily than most people think - it is often more a matter of not being willing to invest the money or the time to find the options.


If you feel trapped, find a way to change your situation.
I worry how you will handle your mother's death when it does come given the emotional baggage you are now carrying.

Death will not be a panacea.
Start working to improve your mental health today, and you will be better off in the long run for starting rather than avoiding it.

Scully,

I hope this all works out for you and your heavy burden of caregiving is lifted off of your shoulders.

'I’m just sick of being the expected answer to everything for my mother. There are times I just wish she would pass away so I could regain my own sanity. She was not a good mother in many ways, but am I alone in these dark thoughts? Am I a horrible person for my thoughts?'

If you are, so am I, because my whole life has taken a turn for the worse since my narcissistic mother moved into so-called AL a few minutes from us and handed responsibility for her life to us. My marriage has suffered (my husband has become her replacement husband) and I have permanent pain from muscle tension. I too am on medication. Now my children are needing help with their babies, and I feel torn, as I don't have the energy for them all.

Kas15's words are very helpful - I have had counselling for a year to try to cope better with my own reactions to my mum, but I am sure I will never be at peace while she is alive, sadly. We just have to decide what we really can and can't do and try to be brave, in my case, about facing the self-centred storms that may arise.

It's good to read that many don't feel this way, but we are certainly *not* the only ones who do, and it does not make us bad people, just honest. I hope things look up for you soon.

My former therapist said it best "You are not your thoughts" I am in the same situation, my mother is 98 and dementia is creeping up on her steadily. My brother and sister won't have anything to do with her at all, not even a phone call on her birthday or Mother's Day. My mom was never on my side when I was growing up, she always preferred my sister who was a beauty queen and married a very very rich man, while I am homely and fat. I am the one here taking care of her now, but I feel deep resentment towards my sister and brother and anger towards my mom because of how I grew up. I think it's one thing to take care of a supportive mom and a totally different thing to have to take care of someone who was never there for you.

All in all, I feel people like us need to be celebrated, because we at least have enough caring in us to take care of someone who wasn't necessarily there for us. I feel what you are experiencing is perfectly normal. It always seems there is no end in sight.

I am in almost exactly the same situation as you for the same amount of time with no family to help. I now hate my mother and wish daily for her death to release me from this hell. She was a s***** mother except for my early years and is now impossible to deal with. Makes my life a nightmare every day with her paranoia, lies and defiant attitude. She puts my life and that of my dog (my only companion) in peril constantly. I have no help for you, just know you are not alone. I wish both of us the strength to deal with this and finally have some joy in our last years. X

I just wanted to respond to MAP2013, with all due respect, I think most of us that are family caregivers are forced into it. I had no choice. I have all of the symptoms that most of the responses on here have, darkness, doomed and gloom, wanting to become an alcoholic, no hope for the future.. You either have to be very rich or very poor to get paid care givers or other resources. My brother and I worked full time jobs besides. We do not have extra time to seek out help, except from friends and cousins that live out of town. I think a lot of us that are posting are not professional care givers, and it seems like most of us were forced into, this is definitely something that I would not choose as a career. So yes, being a forced care giver is horrible and I hate all of it. Most of us are not trained professionally , and we are forced into using medical equipment and other medical things such as wound care in which , I have absolutely no medical training whatsoever in. So I am relived that everyone else is expressing the way I feel and mentioning God. I feel the same way. All of the guilt and worrying about being a horrible person, My heart goes out to all of you. And to the professional care givers THANK YOU for what you do, is there any advice for those of us that are not in the medical field or forced into this?

I am caring for my elderly dad who has vascular parkinsonism. At first things were not too bad but then his walking stopped, swallowing problems has to have thickener & soft foods , incontinence & now he is bed bound.
My breaking point was him wetting himself. He had a pee bottle & pullup pants but he was waking me up constantly fully wet & I became exhausted. I would get stroppy & irritated where I was beginning to hate myself for being like this towards my dad. I wished it would all stop, come to an end but to have that happen would mean death. So I would feel guilt cry & push myself to carry on as everyday. Finally I phoned the social worker who came out & offered respite for a week. Dad goes to a home. On hearing this I finally openly sobbed & said no I don't want him in a home. So Social worker arranged for carers at night & respite with sitters. I have the odd moment feeling overwhelmed but I'm getting more sleep & breaks. I'm finally letting go of doing it all myself. I feel sad for my dad unable to do stuff like he used to but I try to make his life bearable. He has TV /radio 24/7, lots of soft treats, clean clothes& bedding . Hes warm & cosy & safe. He can hear, see & talk so hes still lucky. I say this because my mum had Lewybodies dementia & she couldn't talk or do anything. Her quality of life was just lying in bed squirming . That's when I prayed for God to take her. She finally passed in a home it was peaceful. I felt relief but missed just sitting with her even though watching her suffer alive was torture. So I don't wish my dad to die I just wish the difficult things helping dad would end. But by getting help with difficult tasks & respite to take time out then coping with your parents illness will make things easier.