Follow
Share

I haven't been away overnight without him for 5 years. He has probably had Alzheimers since 2015 according to his neurologist, but diagnosed in 2019. It's hereditary in his family and he was in his early 60's, maybe younger, when it started. He was always so mellow but has anger issues now and will run away. Quite confused alot and has comprehension issues. I fell and had a concussion last June. With family help we made it through but I'm exhausted. I need advice on how to get him to the Memory Care, He also only has about 30 percent hearing with his hearing aids. We toured the facility last week and he did seem to make a connection with one of the directors. He wouldn't talk to me for several hours after.

Find Care & Housing
You can tell him there is a great new place that he will love and you are going to make all the plans for him to move there so both of you will be safe. Buy something nice for his room and don't worry about guilt. You are doing the right thing even if he never realizes that. Get on multiple wait lists if you can.
Helpful Answer (5)
Reply to JustAnon
Report
tblock Apr 28, 2026
Thank you!
(1)
Report
See 1 more reply
I wouldn't speak to him about this at all. Just take him over on the day of, for lunch, and say goodbye, you'll see him soon. He's not going to remember what you tell him a week earlier anyway, so what's the sense? Then you face arguing about it beforehand and him refusing to get in the car on the day of, just in case he does.

There's no easy way, unfortunately. As you say goodbye, tell DH you need time to rest and you'll see him soon.

Best of luck to you.
Helpful Answer (19)
Reply to lealonnie1
Report
tblock Apr 28, 2026
Thank you! It's going to be hard to do but I can't give him all he needs anymore
(6)
Report
See 1 more reply
I'm so sorry that you're having to face this with your beloved husband with early onset Alzheimer's. It makes me so grateful that my late husband had vascular dementia which only has a life expectancy of just 5 years, as early onset Alzheimer's can go on for 20+ years.
Are you prepared to be caring for your husband at home for another good 10 years? I'm guessing not, so you must now do what is best for the both of you, which includes getting him placed in a the nicest facility you can afford.
The only way to "prepare" your husband would be to set up his room in memory care with things that are familiar to him from home, and then give him time to adjust.
This won't be easy, but it will be for the best. Please don't forget that.
I wish you well as you travel this very difficult road with your dear husband.
Helpful Answer (17)
Reply to funkygrandma59
Report
tblock Apr 28, 2026
Thank you so much.
(2)
Report
Don’t tell him anything, as suggested. Just work with friends and family to quietly set up his room and then take him there for a visit and leave him. The staff should help with this ruse and the transition. It won’t be easy but don’t make it harder than it already is by trying to prepare him, convince him, or give him any say in the matter. It is what needs to happen for both of you.
Helpful Answer (13)
Reply to ShirleyDot
Report

Oh lovie, follow your heart . Safety first, is my motto. Rest, rest, rest your mind and u shall find the way home for both you and your husbband.
Helpful Answer (2)
Reply to ChosenRoad
Report

Your husband has Alzheimer's. You cannot prepare him, nor do you need to.
You say he is "quite confused alot and has comprehension issues." What are you hoping to make him comprehend?
You have to make the best decisions for him. This Memory Care is best for his safety and yours. Be happy that he made a connection with one of the directors, that is a happy plus. If he sulks, let him. You can not change that. Are you thinking there are some magic words you can use to make him be happy about this change?

If he does comprehend, just give positive reassurances such as visiting, spending time with him, and letting him know you love him. Tell him he is safe here. Keep repeating it. Tell him you're exhausted and can no longer keep him safe on your own. Smile when you speak of his new home. If you appear anxious and sad and worried, it will worry him. Display positive energy when you spend time with him in his new home.

I'm sorry you are facing this. I am in a similar situation. My husband suffered a stroke at age 53, causing much brain damage. I've been happy to care for him at home for the last 11 years, but I am getting older and getting tired and my body hurts. I am reluctant to let go, but I recognize I will have to sooner rather than later.
Helpful Answer (5)
Reply to CaringWifeAZ
Report

Everyone has their own experiences with this. I am three years in to caring for my now 95yo mother who has some type of dimentia. (I never pushed for specific diagnosis b/c what does it really matter? Each person manifests it differently anyway). I still work FT and travel several times a year. I've been fortunate that the n home i started respites with had always been able to take her (no patient/ staffing ratio issues like the place sge did rehab after bad fall) and one FT nurse there loves her... to the extent she asks that my mom always be placed on her hall and if not possible she came looking for my mom to say hi the first visit back after the holidays.
For my mother I write a note on a white board near her daily things about a week before a respite visit and I just say... on this date MA goes to n home, I go to wherever my trip is, and when we had one, dog goes to kennel. All come home this day. And that board goes to the n home with her. She is trained to refer to them for daily caregivers names and shifts and activities, doctor apptmt dates/times etc. She will review it on her own thru out those days leading up. And we usually dont talk about it. If she asks if tell her im sorry there no one to stay w her while im gone. The last year, she usually doesn't ask. She has written me notes though to remember to hold the mail and paper while she is gone from her home. ❤️

For my father who had alzheimers, he entered memory care n home from hospital rehab after dehydration. We did not really speak of it then either. His younger sister had gone the same route 2 weeks before him, and same memory care. Day of admission they passed in the hall and the :( workers made a big deal of asking them if they knew each other, and that day they did not. That was NOT a good move imo. But my father did not fight being there. I honestly think the dehydration episode really took him down enough that he did not recover enough to be wholly aware. At least he never talked about it that I know of. We did visit as much as possible and I was able to bring the dog with me many times which helped him and brightened the days of the staff, if not the other patients. Im told my dad sometimes knew his sister was his sister, sometimes he thot she was his mother and sometimes he didn't know her at all. I believe he always knew me. He really didnt have all that much contact w his siblings in his adult life, so that would likely be part of the issue.
I agree though.... not much use in preparing them specifically if they cannot at some point understand, and even if they can, dont introduce the permanent part until after it's a done deal. Also, the whole.... this is the last time you will ever be in your home or do this in your home, etc is too much on everyone, you and him. We have to find some way to preserve our own peace/ sanity through all this. Its already hard enough as it is.
Helpful Answer (0)
Reply to Kermit
Report

I'm sorry to learn about your husband' condition. Yes, he requires memory care. Tell him he will have a nice place to live and you will visit him there.
Helpful Answer (0)
Reply to Patathome01
Report

I generally encourage 'leaving the door open' when making these major life changes (moving into memory care). It seems better to me to say 'we'll try it out' vs a definitive moving in - especially if he comprehends what is going on.

I am not clear on (his cognitive functioning / understanding). I believe you need to talk to him based on where he is cognitively. Going into long explanations will / may confuse him and usually people do this 'explaining' when they feel uncomfortable or perhaps sad and guilty. And, keep it short.

If it were me in your place, I would expect your husband to be on an emotional roller coaster (and confused or in-and-out of confusion) as this is very hard on him, too - even if he knows it is the best for him, it is understandable he wouldn't want to go and leave you and familiar surroundings. It is not surprising to me that he was quiet / not talking to you afterwards. He need(ed)(s) time to process his own feelings and the situation he is in (if he can).

He will go through an adjustment period.
If you decide he needs to move into a memory care unit, do make the room as homey as possible with his / some of his furniture, photos.

I'm glad you made it through, with the concussion and I understand you are exhausted. Please do whatever you need to do to take care of you. Get the support you need - find friends that will listen instead of telling you what you need to do (unless you want their input). I intuit that if he moves into a memory facility that you will feel relief and de-stress. It may take some time, although when one is exhausted as you are, there may be some immediate release of emotional and psychological pressure. Be very kind to yourself.

Gena / Touch Matters
Helpful Answer (1)
Reply to TouchMatters
Report

Another option: you can stay there with him for the first few days. At my mom's AL, there is a couple in the Memory Care unit. The spouse has no impairment but didn't want to leave his wife. Not sure if your husband is going into regular AL or the memory care part, but another option to consider.
Helpful Answer (1)
Reply to Jennyjenjen
Report

Could you tell him that you need to be in the hospital for a while and the Memory Care facility is a place where he will be fed and safe while you are away? Emphasize that his moving there will greatly reduce your worries. In this way the spotlight is on you and not on his mental deterioration. You can call him the first days, then if visiting in person you can tell him you can be out of bed only for a few hours, if he still remembers what you said. Many dementia patient associate Memory Care with having become useless and just waiting for the end, and understandably refuse it. You have done all you could, you need to take care of you too. I am so sorry you have to go through it. The time will come for me too to do the same, I know it's very hard.
Helpful Answer (0)
Reply to AnnaKat
Report
donnabeams May 8, 2026
I have a vascular dementia husband age 68 and I am 67 and very healthy. I am planning to move in the memory care facility in an apartment where he will be cares for and also have my company, but I can live a lot less stressed. I am getting worn out and am 99 lbs. I can't lift his limbs and will need more help soon.
(0)
Report
Ask a Question
Subscribe to
Our Newsletter