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I feel ashamed for asking & for feeling this way. Back story: Starting in 1999, I supported my Mom in taking care of my Dad until he died in 2001. After my Dad’s death, my Mom became very dependent on me & so I took on a lot of the her household responsibilities, managing finances, helping her run errands, ect. As the years past & she grew older (& so did I), I would accompany her to her Doctors appointments, cared for her in her home until she recovered after multiple hospitalizations. This continued until she fractured her hip in 2016 & became bedridden until her death in 2018. In 2008, I cared for my Mother in law in my home. She died in 2009 of pancreatic cancer. 6 months after my Mom’s death in 2018, my beloved Aunt suffered a stroke (she suffered another stroke a year & a half later), so here I was again, caring for my Aunt until she died in 2020. It has been 6 years this month since my Aunt died, but I feel that it’s taken me 4 years to process the grief, the overwhelming responsibilities & the mental & physical pressures required of caregivers. Not to mention the responsibilities of being both their trustees. I feel honored that they trusted me in fulfilling & following through with their final wishes. I have no regrets & would do it all again because I loved them so, but I was totally burned out. Ok, after knowing my past experiences, here’s my conflicting dilemma: my husband of 50 years is showing mild signs of cognitive decline & physical changes ex: falling. I understand these could be age related, but I’m feeling frightened & anxious, that I don’t want to do/ I feel I do not emotionally or physically have it in me to take care of anyone else. Has anyone else felt like this, but couldn’t talk to anyone about it? I feel terrible enough on my own, so please be kind.

This is a safe place to discuss this. It's important to realize that you are older now than when all the previous caretaking took place, and that those years took a physical and emotional toll.

So I suggest preparing yourself for what may be ahead by beginning to research assisted living and memory care places nearby, so that when your husband needs more than you are able to provide at this point in life, and at this age (you must be in your 70s or 80s?) you can move him to one that meets his needs, where you can visit as a loving wife, rather than destroying your health trying to handle things alone at home.

In the meantime, if his needs don't necessitate that level of care, be prepared with alternatives such as adult day centers, part-time in-home help, what is available through Medicare or your supplemental, etc.

And make sure everything legal is in place -- wills, POA, access to financial accounts, investment/financial planning -- so that you can both feel protected and have peace of mind.
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Reply to MG8522
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I absolutely understand. I initially felt like a failure when I placed my mother after "hitting the wall", but even all these years later I still shrivel inside at the thought of ever picking up that burden again. ((hugs))
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Reply to cwillie
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Ask a solder why he or she does not want to return to battle.
Ask a (real) law enforcement officer after a gun battle why they have to take time off.
Ask anyone that has been through the "wringer" why they don't want to do it again.
PTSD is NOT just for battle worn military people. Or Police officers
Anyone can experience traumatic stress from any event or events in your life.
What you have gone through demonstrates that very well.
What I would suggest if you have not yet is spend some time with a counselor or therapist just to talk, This is NOT saying anything is "wrong" but what it will do is allow you to vent, to properly grieve. You never were able to do that with everything that came is such rapid succession.
You set boundaries that are safe for you and never let anyone make you feel less than for putting your emotional well being first.
Now, boundaries may move. You may feel differently one day but today your feelings are valid.

And you have to accept that you are older. What you could do 25 years ago is quite different than what you can do now. I have said that if my Husband were still alive and I was going through what I went through 25 years ago I could not care for him now like I did then.
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Reply to Grandma1954
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You should not feel ashamed for how you feel . Everyone has their limits . You’ve done so much caregiving and you burned out . There is no shame in that . I totally can relate to how you feel because I have similar fears about if I would be able to take care of my husband if he needed . It’s the combination of burnout and being older ourselves that is a big part of why the thought of being a caregiver again is so scary. I tell myself I can only do my best if/when the time comes , but it’s still upsetting to worry about failing the one person we made vows with meanwhile going above and beyond for our parents .
So no guilt , no feeling ashamed . You are feeling past and anticipatory burnout and grief . I’m sure there are many here with the same thoughts
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Reply to waytomisery
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Your feelings are valid and nothing to be ashamed of, caregiving is exhausting on so many levels beyond the obvious.
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Reply to Daughterof1930
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Guilt tells you you've done something bad.
Shame tells you you ARE someone bad.
You're obviously not "someone bad" so lose the word shame from your vocabulary when referring to yourself.

Please read MGs good advice and absorb it. And in the meantime, hire in home help as needed. Get out of the house and have lunch with friends. Take care of YOURSELF. Join a book club. Anything that interests you. And don't beat yourself up. Caregiving is exhausting and thankless. PTSD is real, too. See your doctor for antidepressants if you feel sad or anxious too often. ADs have helped me A LOT and I'm only sorry I didn't talk to my doctor when caring for my parents for 10+ years.

Best of luck to you.
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Bellerose63 Jan 30, 2026
Yes!!! I highly recommend anti-anxiety, depression and sleeping meds if you can tk them plus finding a good talk therapist. Before burnout Insomnia kept me from functioning and after 3 days i wouldn’t drive. It’s almost a year since losing mom and husband a few wks apart and i can sleep 6-7 hrs without sleeping med now. I might be taking even less meds at the 2 yr mark of their passing but if i still need them i will continue.
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You matter.
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You have done more than most people could have ever done. You stepped in over and over - it was too much. No, you should not feel guilty. You simply can't take anymore. Your husband will need to go into a facility when the time comes. You need a little time to live your own life. I have been a caretaker to my Mom for many, many years. She is finally in assisted living. Sometimes (often), I feel that I do not emotionally or physically have it in me just to go visit, or even answer a phone call from her. Enough already! I have faced very hard times with my Mom, but nothing like you have experienced. I do not feel guilty or ashamed. Anyone who doesn't understand can take over the job for a couple of months and see how it works for them.
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Bellerose63 Jan 30, 2026
My Mom passed at AL a year ago and when my phone rings my heart still does a flip thinking it’s her calling.
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There is no need to feel terrible about how you feel. You have now been through several gruelling caregiving experiences—that’s enough. You’re older, as well. You are now more aware of your own limits which is necessary for self-preservation.

I would simply research appropriate facilities for your husband, so that when (if) the time comes, you will be ready.

Peace to you.
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I can relate to what you are feeling. I was a caregiver for my mother for 17 years when she was diagnosed with cancer at 58 while being a single working parent to 2 young children 13 months apart & 1 with autism. After my mom passed in Sep ‘22 I finally had knee surgery I had put off and her boyfriend suffered a stroke while I was recovering (he never married & had no children). I became his caregiver for a time until his elderly brother could make other arrangements for his long term care. Last year my aunt’s partner of 25 yrs passed and she could not afford to stay in the apartment she was in, so I moved her in with me in May. In Sept my 81 yr old father who I had only seen a few times over the last 20 yrs needed care so I moved him in with me as well (I am an only child). Then 2 weeks ago my aunt suffered a heart attack in my home, I performed CPR immediately and she is recovering well and headed to rehab for a week or two before coming back home. All that to say I have a wedding out of state in April and my daughter’s 30th birthday at the end of the year which we said we would do an international trip together. I am already dreading trying to figure out the arrangements that will be needed and my dad’s anxiety when I am not around is immeasurable.
I now know it is important to take care of myself first or I can’t be any good to anyone else. At 57 I still would like to live the life I have put on hold for so many years putting everyone else’s needs before my own. My daughter has shared honest feedback about the things she missed while I was caregiving because there are only so many hours in the day and you can only spread yourself so thin. These are all lessons I learned late, but I have learned and am now working hard to keep the balance and boundaries in life that allow both the giving and receiving to happen and ensure my sanity remains in tact. You are not alone and there is no guilt or shame in taking care of your needs.
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Daughterof1930 Jan 26, 2026
Take the trip, you’ll treasure the time with your daughter and have memories to cherish. Your time and life matters
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While I'm still stuck in it, I can say with absolute certainty that I will NEVER feel ashamed for not wanting to return to caregiving once it finally ends. Anyone who wants me to help them is going to have to look elsewhere. Other than college, I've had to help my mom to various degrees for almost HALF of my life. And I'm 33 years old.

Cancer patients don't want to return to battling cancer. Prisoners don't want to go back to jail. People from toxic, abusive households don't want to return to said households.
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OP, you managed to be a Carer for 4 people in succession. That is above and beyond the call of duty. Mentally that must have been exhausting and I am not surprised you haven't yet come through the other side. You are so unfortunate that you are seeing a decline in your spouse but this time you need to get help from whatever services are available, otherwise you will become one of the 30% of carers who pass before the person they are caring for. You need to plan for yourself, you have given so much to others it is time for you.
It may sound terrible that you may not be able to care fully for your spouse but you are older now and most likely declining physically. You have to be pragmatic.

Sending you hugs and prayers xx
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Reply to JudyTeen30
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You are not terrible. It's normal to realize you do not have the energy anymore to care for someone with serious medical needs. Far too many people take on things when deep down they know they are passed that. When my dad was in a care facility I visited pretty much daily (at least four hours a day) for about two years or so. I just cannot do that with my mom. I know it's not hands on, but even with that I do not have the energy to leave the house daily week in and week out. I see her twice a week for only an hour each. I do not apologize for it. We are not kids anymore and we cannot do what we could years ago.
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SadBigSister Jan 30, 2026
You describe my situation and what I am coming to terms with. My 92 year old father is in assisted living and I visit him 3-4 times a week. I bring him food, try to get him out a bit when I can (he has mobility issues) take him to all his MD appts. spend meal times with him but it is draining. I'm 71 and have been doing this for the past 6 years. I feel guilty if I don't spend time with him but I also don't get to do things I'd like to be doing while I still can. It's a tough thing but I think I'm going to start spending less time with him. now.
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I cannot say anything better, or more eloquently, than the others here already have done. But I just really wanted you to know that I think you are remarkable. A truly loving, caring and amazing human being. I have been caring for my 94 year old dad in my husband and I’s home for over five years now, and was helping my mom and dad in there home for about three years before that when they had to give up driving. The emotional toll alone of all the diligence and decision making-the constant vigilance over health issues and safety concerns, the emotional turmoil of second guessing observations about health cues, etc—not to mention grueling hours of cleaning and physically caring with no real break. Ever. PTSD is real. I feel guilty cause some days I just don’t want anyone to ever need to depend on me for anything ever again—my brain and everything else is just TIRED! (And I truly am grateful for all the wonderful loved ones in my life!). You, ma’am, have done this over and over for years and years! I don’t know how you have a shred of sanity left. You have NOTHING to feel guilty about. In fact, being realistic about what you can do at this point is the most loving thing you can do for your husband. It shows great maturity and humility and loving care. I applaud you and pray for
peace and comfort for you and your husband!
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Reply to Hope21
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You should not feel ashamed. You have more than reached your limit of what hands on care you are able and willing to do. You can be the executive manager for arranging home care or facility placement for your husband as needed. Whether he has dementia or is just suffering the effects of advancing age, his needs will increase with time. If you have been married for 50 years, you are of a certain age yourself and cannot be expected to do the amount of caretaking that your husband may require.
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CaringinVA Jan 30, 2026
Well stated and such a helpful viewpoint❤️
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I understand your feelings. I am 70 and spent 5 years caring for my parents with my father at 97 in a nursing home now. Unfortunately it left me with a bad attitude and a lot of regret that I got sucked into their drama in the first place. I should have walked away and let them figure it out. Those five years cost me a lot emotionally, I'll never be the same person.

My 74 y/o husband had a stroke in December. Thankfully he made a full recovery because of the clot buster shot. But in the emergency room that night he was paralyzed on his right side and could not move and could not speak well enough to be understood and I wondered how I was going to take care of this dear man and wondered if I had it in me anymore after all the misery I endured dealing with my mother specifically during my parents' caregiving ordeal.

I decided I would do everything I could to keep him home, but from being on this site I also knew severe stroke victims require 24/7 care and as much as you want to keep a loved one home, you probably can't do it. But I decided I would try. Thankfully he made a full recovery and so we go on as if that night was a bad dream.

You are lucky you had no regrets. My relationship with my mother was in tatters by the time she died. I am so angry that I wasted five years for two unappreciative people and now my husband has health problems. What a colossal waste of time.
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Lylii1 Jan 30, 2026
I understand - I have many regrets as well....
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Hi there
you have a lot in you that you’re containing
You really would benefit from counselling to release the heavy emotions and to talk out your current
Fears
in relation to your current dilemma it may be prudent to get your husband assess
then you’ll be in a position to discuss what options for help- whether that be full time or part time you need
I think you need more than a forum chat
you’ve coped with a hell of a lot that’s bottled up inside of you bubbling ready to explode
it needs releasing

best to you
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Reply to Jenny10
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If you haven’t already, do get your husband to a neurologist. My husband had the same symptoms but refused to see a dr for 3 months as it gradually became worse to the point that, once the FD came and lifted him up and into bed, he couldn’t move. I had to have a meltdown to make him change his mind about going to the ER and at the ER it was DX that he had Hydrocephalus which had damaged his brain because the pressure got so high. Also DX with Dementia. They drained 23cc of fluid and he can walk now but very shaky and spends all day sleeping off and on in his lazy boy. Had he seen a doctor earlier the damage could have been mitigated.
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Bellerose63 Jan 30, 2026
Mine began taking too much pain meds that i learned how to call 911 without his knowing. He didn’t always agree to go w them. I’d put his meds in a ziplock, pack an overnite bag, grab his wallet then call 911. Mine had serious chronic diseases that he wouldn’t take serious so he became a ticking timebomb w me unable to change anything he did or didn’t do.
It’s the worst kind of stress you are dealing with knowing that he’s at fault for delaying treatment and not giving a 💩 that you will be the one looking after him. Shaking my head as i find it hard to stop resenting what he put me thru the 5 yrs before his death. Shaking my head for you, too. Hugs
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I'm so sorry. What I would recommend is that you speak to an actual therapist who can help you work through your feelings and make meaningful suggestions. I feel that anything anyone would suggest here would sound judgemental. Just my opinion.
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Many of us have posted on this forum about caregiving for family, caregiving as a profession or both. We all agree that it is not something you can do indefinitely. It puts you in a situation where you put your wants,needs, and dreams on hold sometimes for years. Many of us are caregivers for much longer than we should be and it takes a toll on our own health and our own relationships. Caregivers by nature are unselfish, empathetic, and giving but what we need to do is to listen to that little voice inside our head that tells us when it's time to stop.
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Reply to Hrmgrandcna
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Finally able to say you are burnt out and have nothing left for indepth caregiving is a positive start. While i was caring for my mom for 12 years who lasted to 97 my husband aged 68 began spending all day napping in front of tv. I knew only matter of time before his heart and lung disease plus diabetes would take it’s toll. It was sooo scary to not know how long he would last w his parents and gr parents living to late 80s/ 90s. Horrifying, really.
I developed major depressive disorder, FMS plus digestive and insomnia trouble. My house became a chaotic disaster and i spent alot of time holed up on my bed watching tv for hours. All this to say PLEESE
don’t let yourself get this bad without getting help. My body became so used to the stress and depression that i still can’t shake it even tho they both passed last spring.
Applauding that you know how your non-caring future will look while another does for husband. Becoming burnt out isn’t a choice we make it comes from alot of time pushing past our limits. We are all supporting and cheering your decision.
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CaregiverL Feb 7, 2026
Everything you say is true…just so much one human can take…they always say the caregiver more likely to die before the patient/loved one
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Just adding more support for you to do what is best for you. We all have limits and it is important to recognize and respect them.
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Some of my family are still angry at me for not stepping in to help my oldest sister. One niece even went as far as posting nasty memes on facebook about women with pretty faces are evil and such. This sister has four girls who refused to do this themselves. I had a limit to only caretake for immediate family. I took care of my mother and younger sister. Later it was my daughter for a brief period and then my late husband.

I work as a HHA and CNA since retirement, but I would never do this for extended family members or place myself in the middle of family mess again. I noticed most of the folks doing all the yapping wouldn't lift a hand in helping. Their method of helping is guilt tripping someone with a Savior's Complex to do the work for them. When it fell into their lap, who do you think they tried to guilt into taking this on? I realized years ago that doors have two sides; in or out.
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Hope21 Feb 6, 2026
I have a cousin-in-law who is a seasoned nurse, but never brought her father in to her home for care, but made other very good arrangements for him and supported day to day. I have had other friends do the same. Due to Covid lockdown and finances and cancer diagnosis, I brought my now 94 year old father into our home over five years ago. He is a wonderful person, but his care is now very overwhelming and stressful. I now completely understand my cousin’s decision!
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It sounds like caregiving chose you for a career, and you did not choose caregiving. You never had a choice. I kind of have had the same history, and now I have to be with my husband. I have a deep fear of his family. Mine have passed on already. My tremor is Parkinson's like. I have never really had it checked out. It makes diabetes testing difficult. I should have a Gexcom 7 but not sure how to finance it yet. I had my dad, mom, grandma, some neighborhood home health aide work with other little careers in between. I just really do not feel that I cannot anymore lift the weight like we were taught in CNA class with the belts. I am short and my back has some fractured vertebrae. But no one around wants to hear "no". Please have your doctor evaluate you for the job at home. Then, you need breaks. We all need mental health & respite. There are healthcare unions like SEIU that are a big help.
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Reply to Octapetty
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You don’t mention how old you are but since you say you’re husband of 50 years, you must be at least 70 ..you have “paid your dues” probably have health issues yourself? If you’re in good health, that’s great but doing caregiving now can really hurt you. So as much as I’d like to avoid nursing home..or if he could use memory care? If possible, hire aide that is capable and trustworthy. Do NOT do it all yourself. Please. 🙏🏼
let us know how it goes. Good luck & hugs 🤗
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It may have been good for your own well being to have declined some of the past caregiving, but you did not know then how you would feel now about it all. So, here you are realizing how you feel now. That was too much that you did. And now you can't do it again. You can't. You know you can't, so don't. I only took care of my mother as her primary caregiver, but I had help with even that. I had helped my mom care for one grandmother, and I helped my father, and my brother just a little. Still, I do not want to do it again. I can though because I didn't do as much as you did. When my husband can't remember the conversations we just had a few days before I get scared, so I can relate to how you feel a little bit. Please stay strong, get him the help he will need when you can't do it, and be his wife, but not his full time caregiver.
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