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You brought them into your home going on 2.5 yrs.Mom is advanced but still talkative, dad is less advanced. You’ve gone through many helpers and are past burnout. You are very close to both parents and adore them. You also have a teen and college aged kids. I’d like to hear from those of you who then made the move ro MC as well as anyone who made other choices as well as kept them in your home. I’d like to know of your experiences and reflections.. I know none are easy choices with each their own pros/cons…I want to learn from you as I’m trying so hard to keep going but at the sacrifice of time with my kids and all else. I tend to lead with my heart but my head is frustrated & sad daily and my body tired. It kills me to see my beautiful mom so lost and tortured. She cries a lot. And so do I.

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I have not been in your situation, though I did help both of my parents at different times with different circumstances. You must be thoroughly exhausted with so much to deal with daily. My only advice is to care just as much for all involved as you do your parents. What you describe often leads to resentful children who see their home and childhood as robbed by caregiving. It also often means neglecting your own future financially, your health, and your emotional wellbeing. Mom and dad are blessed to have your love and care, just know that can take different forms and still protect you and your immediate family. I wish you peace
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Reply to Daughterof1930
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I have not been in your situation but...
Do both need Memory Care at this time?
I know I am one that typically says someone with dementia should not be in Assisted Living but with both of them it may be safer than if it was just one of them.
They would have the help of the staff in AL. They would have each other. Then as the dementia progresses they could both make the move to Memory Care.
If MC is appropriate now then placing both of them together would be ideal. They would have each other and they would still "help" each other.

When I was caring for my Husband I always said that I was ruled by two major organs in my body, my Heart and my Head. And I hoped that when the major decisions came that I would be ruled by my Head not my Heart.
I think at this time making the decision to place both your parents in a facility where they can get the care they need and be safe is a decision to be made with your head but I think your heart will follow. They will be safe, you will be able to be Daughter again not a Caregiver. don't let that fool you though you will be a Care Manager and that is sometimes more difficult.
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Reply to Grandma1954
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While you may not find situations that mirror your own here, you will find many similar ones, so I encourage you to continue on the Forum and explore the questions and answers. It is clear that you are already coming to the conclusion that, no matter how loved your parents are, this isn't sustainable. There comes a time when there is a team of several shifts of several workers on each to sustain safer care for our elders and to preserve our own lives.
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Reply to AlvaDeer
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Many times when it comes to being caregivers to aging parents even people with multiple siblings find themselves being an only child.

When I stopped being my mother's caregiver and moved out, the choices were and still are make it work with homecare or it's a nursing home. I don't offer a third option.

If you're as burned out as you say, then it's time for them to go into assisted living or whatever care facility is appropriate for their needs. There are facilities that offer memory care and skilled nursing and assisted/independent living in the same facility. This way if one spouse needs more care than the other, they can still stay together in the same place. This may be something worth looking into for your parents.

I was an in-home caregiver for 25 years before going into the business of it. I've seen every family dynamic there is and have also seen burnout get to the point where the family caregiver was driven to an act of desperation by the situtation if you get my meaning. My caregiver burnout got to a point when I was living with my mother as her personal servant/care-slave that I was almost driven to hurting myself.

So, I'm going to tell you the best and most truthful advice that has ever been said in reference to being the caregiver to needy, elderly people.

At some point there has to be a choice made. It's either them or you.

Of course you can choose to sacrifice yourself to the bottomless, pit of neediness, elderly decrepitude, and care demands for them until they die, but you will give up and lose everything. You will not be the only person who gets sacrificed because of your choice. You have a spouse and children. They will too. I've seen once happy marriages end up bitter in the divorce court because one spouse moves in elderly, needy parents. I've seen children have their homes and family life hijacked because of grandparents' endless demands and neediness that their parents are trying to fulfill every minute of the day. Don't do this to your spouse and kids. Your first priority is them, not your parents.

Also, your mother is never going to stop crying. If she lived in Disneyland it would be the same thing. You didn't cause her dementia. You didn't make your parents old and needy either. There's a time for all things. Your time now is for your spouse, children, and that life. It's your parents' time to wind down a long life and go into care so they're not a burden on their family.

Please, for your sake and your family's look into residential care for them so you can go back to being their daughter and not their slave. So they can be remembered by the grandkids as grandparents and not the miserable, demented, old creatures that wrecked their home and destroyed their mother. If your parents truly love you and their family and I'm sure they do, they don't want this for you. Put them in care.
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Reply to BurntCaregiver
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ElizabethAR37 Sep 19, 2025
Clearly and correctly put. (And I'm old-old at 88 with a 95 Y/O spouse.)
(10)
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Just wishing you strength and support through these challenging decisions.
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Reply to brandee
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It takes 3 adults to care for 1 adult so who are the other 5 people helping you? and I assume each of you 6 take one 8 hour shift a day? And I trust you are sleeping a good 8 hours of rested sleep a night?
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Reply to Bulldog54321
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I thank you all for your advice, and of course there are so many details that add to the complexity of each situation…but what ‘d like to hear about is how you felt, what ensued, what changed (both positive & negative) after you placed your LO in a facility. I want to hear whether they declined or thrived, whether your relief outweighed guilt, how long it took for them to settle in, what the major impact on them and on you was and so on. And if there is anything you’d have done differently. 🙏🏼
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Reply to Mamasgal
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JuliaH Sep 19, 2025
So, everyone's case varies,it usually takes two weeks without visiting for them to adjust to their new place. There's no reason to feel guilty, just relieved that they are being treated well and safe. You still have to attend to some of their needs, sometimes the staff can't figure out their electronics, phone/TV/DVD. Good thing is they'll get in touch with you if something is wrong. My mother started out in Al but a few months later, went to MC. Because she couldn't see the difference between the rooms, she thought things were being stolen. For example,in the bedroom she couldn't see her chair or refrigerator and in the living room her bed was missing. I think that she was closer to MC than we thought. When in MC everything was in sight, no problem. You've got to understand that your caregiver worries are not the same as they were, much simpler. You had to be the adult and take the appropriate action for their safety. No remorse, burnout or die trying to do the impossible isn't the way to go. They'll accept it with time as long as you make sure they have their favorite things from the old place. You can allow yourself to be the LO you used to be, not a mother hen always running around clucking! They'll complain a bit, sometimes you can bring something special like a favorite food or ice cream to make their day. This will happen more often when they get to the point of not wanting to eat, you'll do anything at that point. But, nobody knows when that is. I was very pleased with the staff handling my mothers incontinence issues and even more so when she became bedridden. You'd be surprised how hard it is to move someone who is immobile, takes two! Everything will work out for all as you accepted the responsibility to do what was right. I have no regrets,many have said that they should have done it sooner.
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My Mom was finally Placed after Many Falls and rehabs after 5 years - it was a huge relief for me ands Passed 3 and a Half months later . My Brother ended up in the ICU for a few weeks and was Placed and Passed 3 and a half Months Later .I Took Care of her May 2016 - January 2017 and My brother July2016- October22,2017 . So I had 2 sick People with Out any Help . Then My Dad got sick . A person can only do so Much .
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Reply to KNance72
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I do not have a similar experience to share.
I just want to remind you to recognize when their needs are more than you can provide for adequately.
You say you are past burnout. You have semi-adult children who probably still need you. It's time to prioritize your time and your energy. Don't make your children last. They have a whole life ahead of them and can benefit from your guidance and support. Don't neglect your needs. You could kill yourself trying to keep up with everyone else's needs, and your parents could outlive you. Who's going to take care of them then?
Finding a care home for your parents is not neglecting them. They can get the care and attention they need while you can continue to be a daughter who is not exhausted, frustrated and burned out.
Spend some time thinking about what your life would look like if they were in a care facility. What would you do with that time? I think you will come up with some answers which will guide you to the decisions that are right for you.
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Reply to CaringWifeAZ
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My 94YO mother who until a fall in May of 2024 was fully engaged in life, often beyond the belief of many who met her. After a long surgery with anesthesia, her ability to think clearly never reappeared. She has been medically diagnosed with dementia. As an only surviving child, I have taken responsibility of her care since my father's passing in 2005. They were married 50 years. After the fall, and after 3 months of rehab, I brought her back home in July to the cottage my husband had built for her on our property. It became clear I needed help. Home health is another subject altogether. Just know you are never without responsibility. Between training the assistants, them often calling in sick, and an unhappy patient, who from time to time would wander out of her house at late hours, I consulted with her doctor for help. It was highly recommended I seek Memory Care. After fully understanding the limitations of MC, I was able to work with her doctor to remove the elopement risk and start with Assisted Living. Which as of November of last year is where she resides. And it was/is the right choice. I toured and interviewed many facilities. And as self pay there are many options. I feel I made the right selection. Although know you are never without often daily responsibilities to aide the facility. So to your point, as an only child, I often refer to myself as a team of "me, myself and I" to discuss these tough decisions. But I weighed heavily on her PC doc who knows her well. And provided me the direction I needed. Best of luck.
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Reply to PepperShaker
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I was caring for my mother nearly 24/7 after her back injury in the year 2012 when she was age 92. I managed her pain medications, provided meals, did all hers and my laundry, transportation to the hospital several times and for senior events and her friends' activities for one year. I got so tired and lost ten pounds while Mom suffered several falls. I had a job for one week after over one year of unemployment. On Easter Sunday 2013, my 93-year-old mother suffered yet another fall that sent her to Kaiser hospital, never to return home again since she was unable to care for herself. Mom was forced into a rehab place, then a CA care home, and she hated it and screamed telling me to get her back home. I could not since she was fragile. After several protests, my OR brother got her into assisted living near him to spend her last one year and three months to die peacefully there. My mother got the best care, and I thanked my TX social worker sister and OR brother to help out Mother.
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Reply to Patathome01
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I am so sorry for the pain you are dealing with. It is very heart breaking to watch your parents go through Dementia. Did you sell their house? Would you be able to find an affordable personal care home nearby? You need help. Please look into moving your parents to a Memor Care facility. Your mom should be place on a medication to calm her. Also, a UTI can cause your mom issues too.

My parents were living together with heart and dementia issues. I was in denial about how much they were declining. My dad was 89 when he fell and had to get a hip replacement. He was never the same after surgery and I had to find a personal care home for him. My mom could not accept the fact that my dad was never coming back home to live. Within months of my dad falling, my mom fell. I kept her in the hospital because I saw she was delusional. Something happened to her from grieving my dad not coming home. She also may have hit her head. I lived 5 mins from their house, but they needed 24 hour care. Anyway, I claimed an unsafe discharge for my mom. The hospital arranged an attorney to represent me. I became my mom's court appointed guardian. My dad died of Congestive Heart Failure while my mom was in the hospital. I moved my mom into a personal care home. Her heart broke and her dementia got worse. They prescribe Lexapro and it helped my mom cal down. My mom died 10 months after my dad because of heart failure. I was visiting them everyday in hospitals an their care homes. Life was very stressful. Please reach out to an Elder Care Attorney and God bless you.
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Reply to Onlychild2024
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I tried for many years to take care of my dad after my mom passed away. Then his health started to decline more and he had many falls. He spent time in the swing bed twice in hopes that he would gain strength to be at home. When he did go home , we had some help but it was still not enough because I was working as well and he had many issues. He then started falling again. He is now in a care facility . I did all I could and I'm sure you are as well but you can only do so much before it becomes a danger to them and to you.
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Reply to faithfulbeauty
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Even though I haven’t had to deal with the situation you are in, I have had to make the decision to move my mother to a memory care facility. She needed more in home help than I could find for her, and my brother, who handles her money, said moving to a facility would also save money. It was one of the hardest decisions I have ever had to make. I looked at several places in the area and found one that really stood out. The day I went to sign the paperwork was extremely stressful to the point where, when I was pulling into the parking space, the phone rang, I jumped, and I hit the car in the next space. I was in tears most of the day. That was ten months ago.
Today I know it was the best decision I could have made and, for her sake, I wish I had done it sooner. She is flourishing there! The programs they provide have kept her involved with other people as well as provide much more stimulation than just sitting home watching tv. She doesn’t remember the activities after the fact but the workers tell me she participates in almost everything and in the photos they take at the time she usually has a big smile on her face. I visit her every few days and sometimes more often and I take her out to eat or to various things I think she’d like. I do have a friend who is a retired RN and has worked as a caregiver with a number of 90+ year olds including well as my mother and she comes with us. I will admit that having her help on some of those excursions makes a big difference. I think she can get my mother to do things I can’t because she’s not the daughter!
I still have to put a fair amount of time into making sure she has what she needs but it is less stressful and I can do it on my time. When she was living in her home I was starting to find myself loosing patience and when I visited her I was doing so much for her that I was growing resentful, even though I knew she couldn’t help herself. Now I can enjoy doing things with her again. I never had to leave her alone to encourage her to adjust as some people have needed. She adjusted very quickly though she still asks when she is going back home. I hate knowing that she will never go back to the house and state she loved so much but she is happier than I’ve seen her in years. I think that moving your parents together would make it easier on them since they would still have each other and wouldn’t be all alone in a new place. Others have addressed that more in their responses. Anyway, moving my mother was the best thing I could have done for her, myself, and our relationship.
I wish you the best, whatever you decide to do.
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Reply to Animallovers
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I think what the next step is. Caring for two elderly dementia patients who fall all the time is really more than a woman with her own household to run needs help. If not an ACF what about a housekeeper - either part or full-time, a visiting nurse. Your Mom's constant crying is part of her illness. You need help for yourself.
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Reply to justoldin25
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Mamasgal: Prayers forthcoming.
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Reply to Llamalover47
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Yes, I've been there with my mom who lived with me for 10 years. At first she was thriving and enjoyed getting out and going to lunch, then in the latter years she just laid in bed and stared at the tv, She wasn't all that difficult to take care of and in the end, there were diapers to change for about a year after she took to a wheel chair. I would sit on the couch in my special spare time and read to recharge. Is there anyway you can delegate household chores to the other family members, so you can recharge. You have to take time for yourself. Here's another idea...I know in home health care is expensive, and most don't stay overnight. Some are covered by Medicare but it doesn't cover enough. However, there is an option and that would be to hire in a nanny type person to live with you and help with the parents. You could also look for a college student that needs room and board while going to school and that would be a win for you both. While she couldn't be there 24/7, it might take a load off you to have someone help. Yes, the burnout is real. I took a short vacation away w a friend while the hubs took over.
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Reply to Evonne1954
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Hello. I just placed my 64 year old significant other in a nursing home that is sub par, but I had no ability to choose due to his financial situation. I am his health care agent. I was burnt out, and he kept falling and getting injured. He has vascular dementia and other serious health issues. My feelings were mixed for several months thinking that maybe I could keep being his caregiver regardless of the insurmountable stress that I felt. I was sleep deprived too. Finally, I realized I wasn't helping him or myself. His Doctor said he was dying and he may not survive the year, especially if he had a fatal fall. Also, hospice would not accept him, and I had no help. So after his last fall, I put my irrational thoughts aside, and worked with the hospital to have him placed. Being in denial is a strange thing. I am not a professional caregiver. I miss him everyday, and I am very sad. He was already moved into the special care unit because he needed more care than what a regular unit could provide.
I am sorry you have to make these decisions. All of your feelings are valid. We all process pain and anguish differently. No one can tell you what to do.
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Reply to Dorothy68
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I simply cannot imagine doing this and caring for your teenager on top of it all. I dealt with the care of my parents who were in their early nineties when they started to need help. My only child is in her 40s, I am married but have no parenting responsibilities. . I cared for them every month for six months at home. My father had cognitive issues, my mother heart troubles, arthritis and the accompanying mobility issues from it. They both used walkers and my mother was a fall risk. Their health kept getting worse and worse.

At the very least you need to get some help in or place your mother in memory care. I hope your mother's ordeal is over soon. That's the only thing you can hope for because she is not going to get better.

We are now in year three of nursing home care for my father, my mother is now gone. My father is nearly a vegetable, just eats and sleeps. Doesn't really respond much to me anymore. I hate visiting him and I cannot wait until his body gives up. As far as I am concerned, he is gone to me already. But there is no end in sight. He will be 97 at the end of October and his body just keeps going.

My retirement years have been full of stress and long distance trips to NYC. I resent the lack of appreciation for what I and my sisters have done for them. We did a lot to keep them home as long as we could, and they really treated us badly those last years, I am hoping that some day I can remember some happier times but so far I can't.
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Reply to Hothouseflower
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