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My mom has dementia (partially) and Parkinson’s. She is immobile and has to be carried or pushed in a wheelchair. That’s not the hard part. The hard part is her neediness. She’s constantly asking for the same things and states the same worries. What I don’t understand is that sometimes she can be very coherent. Then some stressor triggers her and here comes the nagging and drama. What I’m struggling with is feeling any sympathy for her. She has never been mean to me. But she’s always been emotionally unavailable to me. I’ve always felt like I had to be perfect for her to love and accept me. I didn’t realize the pressure this placed on my life until I had a breakdown a few years back. Now that she needs me, I simply don’t have any desire to be there for her. She didn’t willingly take care of her parents (who both had dementia and one also had Parkinson’s). She would step up if asked but never with a cheerful attitude. I remember this. She’s never been a cheerful person. I know life hasn’t been easy for her. I just wished we had an emotional bond so I can care for her out of love. Right now I’m resentful and really don’t understand why I can’t get over it and just be there for her the way a daughter should be. I’m seeking replies from those who have any understanding of where I’m coming from. I don’t need judgement. I’ve judged myself enough.

You don't need to do this, and in fact you shouldn't do it just because you think you should. Move her to the appropriate level of care facility, and reclaim your life. A mother who loves you would want that for you. See an elder law attorney about how to pay for this, if necessary. (In case you need more persuasion, doing all the lifting in and out of her wheelchair, bed, etc. plus toileting or diapering, and bathing, is going to end up ruining your health if you continue to do it by yourself.)
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Reply to MG8522
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My kid was pulled into the realm of life and caregiving..she had no choice.. the only choice she had was to visit a grandma. Do you want to visit The Who knows who you are and can say hello? Or the one who gazes aimlessly and doesn't act act like she knows what is going on???
You have a choice. You need to go with one of your parents and visit one if your grandmas... I suggest you visit the grandma who can speak...and knows who you are by name.,,,
Life lesson....

When ALL ELDERS have deceased, includes her dad,.... she is basically done...
"Do not expect me to "care" for you."
and I don't.. she is busy creating her own life.. heck, I didn't go through all of that as a kid..,
Grandparents were in another state. Saw them once every 5-8 years.. I was not involved in any of this caregiving scenario.. only what I heard my parents say.. I did not get to hear about my heritage from my grandparents. I missed out.. with that being says, my mom felt guilty by not being there when her parents were going through this. She did go and visit, but she couldn't stay for the long run..same with dad...,
So....
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Reply to MAYDAY
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MG8522 said it correctly. Find mom a good place ALF..
you can the concentrate on the things that need to be done; like, being there for your mom as a daughter, living, loving, and caring.. you don't need to stay in the facility for any longer than her energy allows...
mom may be getting tired snd needs to rest.. take her cue of grumpiness and excuse yourself..I forgot I have frozen food in the car, I must go..
don't forget to leave her treats and for her caregivers.. even if it's just a roll of Lifesavers...! But then again they may be a choking hazard..⚠️
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I think I was in the "sandwich "generation." Taking care of our parents, while bringing up our child,.
My friend is in the "Club Sandwich " scenario, taking care of parents, wanting to see her kids, and needing to see her grandkids!! I certainly could not juggle that.. I barely could juggles the Sandwich scenario.,
We csn only handle what we can do. Geez, can you imagine what Joe is going through ? And yet, Jane is doing this., ya, I don't know.. some people have more superpowers than others, I certainly can only handle a little.,
most of my plate has been emptied; everyone is gone, except my child who says I'm on my own. She's been there done that.. she's done..
I don't blame her.
. I have my living Trust and DNR, and POLSTand POA Directives on paper.. TAG SHE's IT!
😬🤣
Did I just put all that on her??? YUP!

I absolutely trust that I too will leave this earth.., hopefully with love , kindness, snd laughter ....
just be nice, appreciate the little moments, tell your LOs you live then, thank you..
THSNK YOU! Even the lil misspellings,

when was the last time you saw a double rainbow?
What was the difference between them? Weird, I noticed it., nobody else noticed until I pointed it out..,
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First I have to say that I chuckled when you said that your mom has only partial dementia. There is no such thing as partial dementia, though she may just be early in her dementia journey, as yes folks with dementia do have good and bad days.
And just so you're aware the dementia that usually goes hand in hand with Parkinson's is Lewy Body dementia which is the 2nd most progressive dementia with a life expectancy of just 5-7 years, so she will go down hill quickly and will be much harder to take care of.
With your justified feelings, it may be time to look into getting mom placed in the appropriate facility where she'll be looked after 24/7 and you can get back to just being her daughter and not her resentful and overwhelmed caregiver, as I have a feeling that you'll only grow more and more resentful as time passes and that isn't fair to either of you.
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Reply to funkygrandma59
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"Lewy body dementia is a progressive brain disorder that affects thinking, movement, behavior, and mood"

Dementia also robs you of empathy. The person can get self-centered. Lewy body can make people aggressive. IMO, if your Mom is now in a wheelchair and Dementia has set in and you don't feel you can care for Mom, time to place her. I would say Longterm care because she will only get worse. She is too much for a private Assisted Living or Memory care. I would say a nice Longterm care that takes Medicaid if she has no assets. I agree that you need to talk to an Elder Care Lawyer.
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Reply to JoAnn29
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Please stop being a caregiver for your mother, it’s unhealthy for you both. A resentful, unhappy caregiver will never be a good one. That’s not said with judgement, it’s just a fact. Your history with mom prevents you from being the right caregiver for her. Time for another plan for you both, no apologies needed. Call the local agency on aging and find out about her options for care, also her doctor, and a local social worker. Remain firm you cannot provide care. I wish you both peace
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Besiberri Oct 3, 2026
I am a 62 year old man taking care of my mother with Alzheimer's diagnosed 14 years ago. At home. Full-time, 24/7, no aids.
I am a terrific caregiver. A real beast.
I even work out at home every day since I can't go to a gym.
Do you think I am happy with my life?
For goodness sake.
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Her health (or lack of it) is stealing your life. Why wouldn't you resent it? It's normal to feel that way. We aren't all meant to be Little Mary Sunshine!

My mother liked to publicize that everything was wonderful between us, but in my mind, it wasn't. She had dementia (fully, LOL) for 5 years. It was terrible to see her suffering, and I was much relieved when she finally passed at 95. I managed her care, performed some of it, kept the business going to support her and dad, neglected my own work, navigated other pesky family relationships on her behalf, and yes, I resent it all to this day. She was married to my dad for 70 years but didn't help me with him at all when he was dying. When I asked for help (that she wouldn't have had to do herself because she had an employee she could have spared to grocery shop for dad and me one afternoon a week, which is what I was asking), she refused while telling other family members that she just couldn't think of any way to help. She wrongfully attacked my character when I was only 10. I cried for days because of what she said, still get teary over it sometimes, and I never felt the same about her after that. I was the scapegoat who caused her to get a cold at the school Halloween carnival because if I hadn't been going to school there (no choice, so ???), she wouldn't have had to help with the go-fish booth (her choice, but somehow my fault, so ?????). She lied about me to family members when I was an adult, disliking me for something I didn't even do; it was all made up in her head out of need for attention, and she got a lot of sympathy for her "pain." She was addicted to pain pills and tobacco during my childhood, which greatly affected our home life. She had an affair when I was a teenager, disrupting our household considerably. As a child, I didn't realize how unstable she was overall. I learned early that at my times of greatest need, I couldn't count on her. Then caring for her in her final illness stole 5 years of my life.

So yeah, a lot of us have had stressors as you do. We survived. I moved my family 900 miles away from my mother when my kids were tiny tots, and it was the best thing I could have done. We then had a better relationship because she couldn't feed off of my daily life to create drama.

You say you can't "just be there for her the way a daughter should be." Well, how should a daughter be? You get to decide that. Your kind of daughtering is up to you. My kind was to move far away and maintain a friendly relationship because of my kids. Your kind might be to stop speaking to your mom. Or limit contact to infrequent visits in her care facility, no phone calls, no sappy kissy huggy stuff.

Please let us know what you decide to do!
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Beethoven13 Oct 1, 2026
I couldn’t have said it better. Exactly this. Adult Children of Emotionally Immature Parents has been helpful to me, author L Gibson . Also J Wise.getting your dependent parents out of you. I lived 1000 miles away my whole adult life, only visited. I got sucked back in when they were in the 90’s due to their health problems. It’s been a learning curve. In general, stay away, manage from a distance, hire caregiver support and if no other option, place them in care facility. Don’t sacrifice your own life.
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I was not the primary caregiver for my mom. I did visit her regularly (about once per week) for the final four years of her life. We did not have a close relationship; she did have close relationships with my sister and my older brother. I mostly made my peace many years ago with the nature of my relationship with my mom. What I do resent is that my siblings put all the blame on me for the nature of my relationship with my mom and do not acknowledge the role played by mom's nearly life-long mental illnesses, which severely affected me when I was a child.
I accepted (again, not entirely but for the most part) that I did not have an emotional bond with mom. I got through the weekly visits by thinking of them as a job. I knew the job would end sometime, and it did.
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Tiger8 Oct 3, 2026
I am so sorry your mom treated your siblings better than you! Your life matters! You matter!!! I am in my late 50’s, and I wish I could rewind time, and adopt you from your mom, and give you the love and attention you always deserved. You are strong to try and get past the hurt, but it is always on the back burner. Please feel me sending you a big bear hug!

Just learn from others and follow the good they do, and leave behind the bad things others have done. I do not know why your mother behaved this way? Maybe you reminded her of a relative she never liked. Regardless, there is NO EXCUSE. Look in your mirror, and know in your heart that YOU did nothing wrong, this is your mother’s loss. She missed out on all the wonderful love you would have had for her had she been deserving. She made the choice to behave this way, not you. You were the victim of an unfair circumstance, and childhood forms us for life. Stay strong, and know that the hurt she caused you, was truly her loss. ❤️
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You shouldn't have to be her care giver.
It also sounds like she has cold mother syndrome. That's a thing. Ive spent my life trying to figure out why I thought my mom didn't love me.
You've already had one breakdown.
You need to continue taking care of your needs and mental health first and get your boundaries in place.
Take care.
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Regarding Besiberi's post: Martyrdom is a choice. I don't support it.
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MG8522 Oct 3, 2026
Besiberri has posted here multiple times about his deep misery and ongoing resentment, but refuses to make any changes. His martyrdom seems to be his identity.
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Normal people feel resentment when they give up their entire lives to care for a sick parent. Even when that parent was wonderful to them. They can swear up and down they love caregiving and all the nitty gritty details involved, but they don't. They do it out of a misguided attempt to be loved and helpful and to repay that parent for changing their diapers as a baby. Some insist the Only way to show Love is to sacrifice your entire life for the parent. I'm here to tell you it is not. There are many ways to show Love besides changing diapers and carrying your mother around. You deserve a life of your own while still helping mother out sometimes.

She needs professional care now by a team of caregivers. You can go back to being her daughter again and relieve yourself of some of the resentment that goes along with 24/7 caregiving. Because one day you can easily hurt your back badly from carrying the woman around! As we age, our spine is not meant to carry such loads. In care, they have Hoyer lifts to do the heavy lifting. Please realize you're not a one woman care team. Look out for yourself now while still loving and helping mom with her new needs in managed care.

Wishing you good luck and the ability to realize that YOUR life matters too.
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Reply to lealonnie1
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This is a very difficult situation for you. You don’t need to have your mother take advantage of you. Does she live with you or in her home? She could live in an assisted living or memory care facility where the staff helps her, then you can be just her daughter or son.
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One of the responses here mentioned the possibility of Lewy Body. I know it can be involved with Parkinson's. My husband had Lewy Body, he was dead in 2 years after being diagnosed so it was not a long slide but it sure was quick. He could change into a whole different person 2 or 3 times within half an hour. I literally never knew who he was going to be from one minute to the next. After a really nasty fall which required hospitalization, when it was time to discharge him the doctor's told me DO NOT TRY TO TAKE HIM HOME. I did consider doing it but based on what had gone on before the fall I realized that they knew what was best and reluctantly agreed to place him. It was a terrible experience for me to see him in that place and I can only imagine what it must have been like for him. I went every day, tried to put a good spin on it but it was awful. I was able to apply and get him into the VA Nursing Facility only a 5 minute further drive. They gave him fantastic care, I know that isn't an option for everyone but there are good places out there. I know I made the right decision even though I really wanted him home, but I also knew no matter what I wanted it wouldn't have been good for either of us. Believe me he wasn't happy with me but he did gradually come around about being there. I would like to think he knew I wouldn't have been able to do it alone, but I really think he just lost all ability to rationalize anything and just dropped it. I would definitely get her into a skilled facility, it will be better for her and better for you too. It's a hard road to be on but somewhere we find the strength to keep going.
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I took care of my husband at home for 9 years after his stroke and dementia diagnosis. When he was finally completely bedridden and I could no longer care for him, I placed him in a Family Care Home. He is getting the care he needs, and I feel as if I were released from prison at age 89. My health is still good enough to do the things I enjoy. And yes, I resented taking care of him. He was a not a good husband or father. Our children seldom visit him at the facility even though two of them live close by and the other two don't go to see him when they visit me. I hear what you are saying about being judged. His present caregivers and those who didn't know him before are judgmental of me but those who did know him understand where I am coming from. They wonder why I put up with him as long as I did. My advice to you is to place her in a care home as soon as possible and go on to enjoy your life. I don't feel any guilt, and neither should you!
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Fawnby 2 hours ago
LucilleJ: You go, girl!
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I don’t want my kids to be burdened with my care one day, but I also don’t want to sit with a drool cup in the corner, while some worker who could care less about me, prepares to do a lousy job of wiping my butt.
I do not ever WANT to lose my abilities , and I doubt any elderly feels any different. It is just part of life. Just like cars can run for so many decades with repair and care, or they can be scraped because of neglect.

If parents acted like this when they have children with disabilities like autism, cerebral palsy, muscular dystrophy, childhood cancers, etc,,, it would be so sad.
You could make the same arguments, and say, we are a healthy young couple that never asked for these hurdles, problems, extra work. This kid is stealing our lives away from us, it is not fair, etc….

This is just not the way family should treat each other. Look at how the loving and caring parents that have worked extremely hard, to give their child the best life possible.
So many of these children with disabilities and diseases, have achieved phenomenal achievements just in the special Olympics alone. All with the love and support of their family members. Do you think this was easy for them or the life they would have chosen for themselves or their children? This is just what you do when you love your child. Why would you not do the same if you love your parents? I am sure many parents are beyond unworthy of this type of commitment to their aging and health conditions, but so many are more than worthy of the love and care. Everyone just has to decide if their love for their parent/parents is worth the commitment of help, support, and love.
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SnoopyLove Oct 4, 2026
Drool cup? Special Olympics? What the hell are you even talking about?!!

You don’t seem to be interacting with the content of the OP’s post at all but just going off on your own spiel. To me it seems callous and unfeeling. Kicking someone when they are down. Someone who wrote frankly on a forum about the difficulties of caring for a frail parent is worthy of your scolding? Why do you feel the need to do that? To make yourself feel better at her expense?
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Your previous relationship with your parent does impact your patience and stress level taking care of them later. I wish I had more time with my Dad and would have moved him in with us in a heartbeat to take care of him, but he just dropped dead at 90 (independent, but on the precipice as all sorts of things were starting to go wrong). My relationship with my mom is complicated and I’m solely responsible for her, now 7 years later! My fuse is short, I’m resentful at times, she’s always been emotionally unavailable and when she has reached out to me for emotional support, I have a very hard time. The well is pretty dry and that’s on her, not me. Don’t blame yourself. And parents, don’t expect loving support from your kids if you didn’t establish a loving and supportive relationship with them before you needed them. “Duty” is irrelevant.
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I know that feeling of resentment, a lack of closure and a lack of an emotional bond that should be there between mother and daughter (caregiver). It seems to have happened to a few caregivers that are friends of mine. I have taken care of both my parents in their mid 90s in my home until both had dementia. I have often been told that I should forgive and I should not be resentful and I should be happy to have my parents and take care of them. It kind of hurts because other non caregivers only look at what your parents are going through and I feel that as a caregiver I am invisible. Resentment is a normal feeling when you are expected to give care to your parent(s) without gratitude and love and most of all caring for yourself and doing those things that give you joy. There have been times that I felt so many emotions, guilt, shame, resentment and the loss of that emotional bond. For my own mental and physical health, I needed to find ways to take a break regularly from caregiving by hiring a professional caregiver or assistant living facility, set boundaries and literally walk out when I would hear the nagging and drama associated with a visit to see them. My elderly mother would leave horrible messages on my phone, write notes to me that she hopes I go through all of the horrible things she's been through. My dad continues to complain that he hates being where he is. I've moved him three times to different facilities to satisfy his needs. I learned that there is nothing I can do to make them happy and it is not my responsibility. Unfortunately, I allowed them to take over my life for many years, but I feel I am more at peace now. You are a lovely compassionate person who really cares, but you are the one who needs care as I did. I sincerely hope you find your happiness.
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Reply to Freedomtocreate
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Absolutely. I resent that Mom didn't assign a power of attorney. That her HCP only said, "my kids know my wishes." That she spent money unscrupulously and left herself with a small monthly income. I resent that her husband of 40 years didn't take some of that money they made off their stocks and buy a house that someone in the family could have moved into to care for her, or could have been sold to give her more money to work with with care facilities. I resent that over the last SEVERAL years, I repeatedly told her I was concerned that she needed to see her doctor about her memory issues (I left out that she was starting to not be able to learn anything new or have her memory jogged). I resent that she is not the sweet, peaceful, gentle type of dementia but the wild, aggressive and entitled type.

And I resent that I resent all of this.
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