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And you need more time for yourself. Please prioritize what you are doing for them and choose the most important things. You can't do it all. The staff is there to do the fetching and carrying. The hired help is there to do that too and could help with laundry.

You can't continue at this pace. Back off and do what only you can do like the the bill paying. List activities for the hired help. Could they check medications? This is a change and your parents won't get the same attention you gave to them at home, but it is about getting their needs met, and keeping them safe. Not all their wants will be filled. That's life. It's also about getting your needs met. You need to keep yourself healthy.

I agree that the staff there will not do things if they see you doing them. Let go of trying to do it all.

Be aware, although it is not ideal in some ways, they may need to be in separate facilities. As we age and develop more and more health conditions, our choices become more and more limited. Sometimes it's a choice between bad and worse, not good and better. It's a shame, but it's a reality most of us will face at some point. As Bette Davis said, "Old age is not for sissies." Neither is caregiving. You have to be tough for both them and you.
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Perhaps you need to find a place that provides higher care that will take them both. Eventually some place had to open up a room to accommodate the 2. I doubt this is the first time a couple has wanted to stay together in a facility. You might have to wait awhile. Maybe you can talk to facility directors about exceptions with them sharing a room but with some rules they may have? They can have a room open for an extra patient
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My mum took many months to recover from her stroke, not 8 weeks, so it isn't a given that this is the limit of her improvement. Yet, it might be. Mum developed vascular dementia, which is common following a stroke, and she slowly went downhill again. Mum was 30 years younger than your mum.
I'm not sure why you want to buy your parents' home. If it's so they have somewhere to return to, I think that ship has sailed. Just sell it and use the money for their care and their growing needs, as well as for your release from constant care duties.
It isn't just your parents' lives which have diminished, but yours too. They've had their lives; now, it's time to live yours.
You can't make everything perfect for your parents. Sometimes, they'll be stuck watching something they're not interested in because they can't work out how to use the remote, or they'll not have exactly the meal they want because they didn't state a preference. Little things don't matter - just that they are safe.
You can't be there all the time. Either this is the wrong place, or you need to hire extra help throughout the day, using money from the sale of their house. You shouldn't be there all the time.
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It's definitely time for memory Care. Assisted living is still living alone. Usually in memory Care they are taken to a large room with lots of people around and caregivers always present. They are brought back to their nearby rooms to rest and get cleaned up. Memory Care is appropriate for people who still have some memory but not firing on all cylinders as you say.
As my sister once said "letting auntie live alone and make decisions because she sometimes has good days is like letting drunks drive because they sometimes make it home."
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Also with the house bussiness, unless you want to move into it, or keep it in the family I would sell it and as many of the possessions as you deem fit such as couches etc or trade out with your items selling yours. If you want to keep say your parents dining table set then sell yours. You would sell things faster Especially if you sell the items for a good lower but not way uneer value prices vs top dollar resale value. Many times second hand stores will buy everything for a set price. Prices should not rip you off but must give them room to resale. If you do that have an idea of what you want for each item but also as a whole so if they do pick and choose items such as if they say they would take the dining furniture sets, the beds, and all the living room furniture but don't want the couch, chairs or decor if you have an idea of what you want for each item it makes it easier to come up with a price to start negotiations. Research any antiques and jewelry they might have and take those to antique and/or jewelry store.
If you want to help others giving individuals an opportunity to purchase first you can have an estate sale or auction or both. If they have a large number of possessions it might take 2 different events. Then put the house up for sale. Again I'm suggesting this for anything you or your siblings do not want to keep or your parents won't need. Something will have to be done with it someday anyways. My as well be able to use the money to help care for them and yourself.

If you need a fast sell on the house/property I wouldn't do a reverse mortgage to get rid of the home. If a fast sale is necessary You'd be better off contacting one of those individuals or companies that buy homes in any condition. See what they offer you. They typically pay all closing costs and take care of the paperwork etc.
To get the most money I would try to sell it myself. Advertising it for sale at the sales or auctions for the other possessions. Then running an ad, putting a sign up in the yard. Then if no luck after a certain number of months you cam list with a realtor. You can also auction it at an estate sale or auction starting the bid at the lowest price your willing to take for the home keeping in mind any costs. Your first step is going to be an appraisal no matter which way you go. I would definitely start with the possessions inside. Otherwise your going to have a house full of furniture and belongings with no place to put them or the extra expenses of a storage unit and costs of moving trucks etc to move it. Anything left over you Can donate to goodwill, salvation army etc but I'd start with homeless and womens shelters, teen homes, halfway houses and places like that that seem to be more available for the needy. Especially coats but some will take furniture pieces too when helping people get off streets to a home like HUD. Or the teen shelters etc. And your parents can know that they helped those in need too while helping themselves.
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Just to update Mom and Dad still there, I hired private aides 10-2 and 5-8 for several days a week who have been wonderful - although one just left sadly -and I fill in the gaps esp on weekend days but I do prompt Mom on those days to call the facility aides and ask them to take care of them as there is "no private aide today". I took several months off work with FMLA. I still go over almost daily. But I do back off too when I feel I can. Sometimes I go just for a short visit, sometimes longer. Mom had several issues over these months including bad diarrhea at times (meds were not right, took forever to correct them with facility and dr) a bad "diaper rash" that wouldn't heal and she didn't get the right creams until two dr visits - it is still is a problem from wearing Depends at night. The private aide alerted me to it, not ever anyone at the facility. Some facility aides as good but as several of you mentioned it is AL not LTC and they are in and out as fast of the roomas possible sometimes cutting corners leaving my Dad dirty after number two or leaving Mom alone on toilet when supposed to be supervised. Mom HAS continued to improve so those of you saying 8 weeks is good as it gets, well you are wrong. I say that because I want to give others hope. I push her to walk with her cane or do her exercises and I get Dad to walk down hallway every day with the private aide aws facility will only put him in wheelchair all the time. Mom still has OT and PT as keeps improving. I have to think it is also due to my care in between. She isn't what she was mentally but she is MUCH better and able to text with me and keep me posted now. Sometimes her short term memory is not good. Sometimes she mixes up staff names but understandable as there must be 20 different ones who come and go by shift or time of day, at least 4-5 different ones a day. So the private aides are indispensable to keep me updated, monitor, provide companionship, change or help toilet on time and watch for rashes, etc etc etc. Still investigating other options as it does cost a fortune to do two people in AL plus many hours of private aides. But for anyone who says don't do it, I can't leave them sitting alone for hours and hours a day just staring at the TV (Mom doesn't initiate to go to activities and many are during their meals, naps or bathroom times) and sometimes in dirty depends or with an itchy bottom or sores or whatever and without a glass of water even at their side, and having no one to talk to. Just can't do it. Might sell house although have one lady who really wants to do live in now for them who has done before. But that is a HUGE decision and for sure not permanent would have to move Dad or both to LTC anyway if they deteriorate as AL is not going to cut it even with extra aides. Unfortunately there are not many others at this facility who are mentally sharp as my Mom is to make friends with and her hearing is so poor it is very hard for her to socialize. Dad is unable to converse at all but he can answer simple questions. Thanks for the inputs!
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MG8522 Apr 27, 2025
Thank you for taking the time to update!
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Most facilities suggest you do not attend to visit for at least two weeks.
Certainly in your case this is required because you BOTH --you ALL --have formed habits that must be broken.
Speak with administration how best to accomplish this.
There will be no solutions as long as YOU are all the solutions.
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It is great that you were able to place them together. That can be difficult to find. I just placed my father last October. I could not place my mother with him because she cannot walk or stand and needs a Hoyer to move. I think it is pretty normal to have a little (or a lot) of running back and forth for the first few weeks and maybe even months. But, that should settle down as you hand off more to the staff and they get to know their needs. It will never be zero, but it should get better. It is hard not to hover when they first go. That is not a bad thing because you still need to be vigilant about their care. Al’s and even SNLs do not always do a great job at monitoring hydration and nutrition. Assuming they have a refrigerator make sure they have bottled water or other drinks they like. I open the caps so they don’t have to struggle to twist them open. Visit at some mealtimes to see what they are feeding and make sure they can and are eating. Discuss any concerns re these two important areas with the Director. Make sure they are encouraged and included in activities they can do. I keep a BP cuff, O2 finger monitor and thermometer in my Dads room in case I need to check those things. I also have a couple COVID tests stored in his room. I have had to use these things when the staff failed to notice he was not doing well back in February. But, as far as routine day to day, things have gotten better. He is still adjusting but socially, it is a big improvement for him. Good luck!
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