Typically how long will transition take after move to MC?

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Typically how long will transition take after move to MC?

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We moved my dad to a MC facility 2 weeks ago. He has went through a lot of changes in the last few months. Losing my mom unexpectedly and moving from his home in AZ to a MC facility near my family in WI. He is in mid stages of Alzheimers, he is very physically fit, but cannot live alone. He calls me multiple (15+) times per day. He tells me every day he hates it there and wants to move.
Should I expect this transition to take at least a month. Will he possibly relax and adjust?

Alzheimer's & Dementia Care Decisions Memory Care Moving

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So sorry for the loss of your mom. Your dad sure has had a lot of changes. It may take him longer than 1 month to get comfortable there. Who knows? Does he remember that your mom is gone and is mourning her? Are you able to get over there much to visit or do they not recommend that? Seems to me that helping him get into the routine and getting him participating in the activities available to him would help him adjust to his new place. Also getting to know the other residents will help make his life so much nicer is he has a friend or two.

15+ calls a day is obviously excessive. I would not answer that many. Maybe answer 2 a day and ignore the rest. He has to learn to rely on the staff and not so heavily on you.

It is certainly possible that he'll adjust. He may hate it and want to move at this moment but I bet he'd say the same thing about any place you moved him to so just stick it out. Dementia is horrible and I bet it is very hard to be happy.

My mom has mild/moderate dementia and is in assisted living with extra levels of help to compensate for her deficits. Luckily, she adjusted pretty quickly. I moved her there after living with me and hubby for 7 years. It just progressively got to be too much for me. Even with caregivers.

Best of luck.

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Please find out if there is a geriatric psychiatrist who consults at the facility.

Given that his ability to "understand" all these changes is irretrievably broken due to dementia, meds to calm his agitation may be the best solution available.

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Thank you for your reply. My husband and I visit daily and we have been taking him out to dinner each week. But he seems to almost act entitled, I feel shameful saying that because I know it must be horrible for him. I also know he would not be happy anywhere, he wasn't happy in his own home and called me multiple times a day asking when he could fly home to be with me. And then wanted to leave my home the day after arriving.
The staff does recommend family visits as much as possible so the resident does not feel abandoned. He is confused with time and thinks my mom passed away 12 years ago. I am realizing I need to set boundaries for myself, he is very dependent on me which is not allowing him to make friends or participate in any activities.
Thank you again!

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Wow, this could be my mom. Moved her from Florida to Washington to live with brother during COVID. She has mid dementia and was calling everyone all day. She was in WA for 2 years. Brother and SIL had to return to in office and were in an area hard to find in home care. Moved her to an AL near me in Colorado. She has been there 9 months and still calls me multiple times a day to take her home. I see her 2 to 3 times a week. I take her to various events, usually musical theater and horseback riding. I hired my dog walker to take her out twice a week. She doesn’t remember doing anything literally 5 minutes after the event. She is still unhappy and doesn’t think she needs to be with “those” people. She is 89 and in perfect physical health. She could easily live to 100. People told me she would adjust in 3 months. I don’t think she will ever adjust. Good luck. No one has the answers.

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IMO, he will not adjust if you don't back off for awhile, everyday visits are way over the top. You are interfering with the acclimation process.

Your facility is the first that I know of recommending so many visits at the beginning of the process, the 5 I have dealt with all said the opposite.

You should stop answering all the calls as well, one a day should suffice unless there is an emergency.

Set some boundaries, it will help both you and he as well.

Let the trained caregiver's do their job.

Read around this site, they all want to go home (wherever that may be in their minds), most also hate the food and anything else they feel will work to get their way.

Good Luck!

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Please consider this.

You have no real way to “know it must be horrible for him”, because you don’t have dementia.

Most (if not all) people entering MC because of circumstances like your father’s react negatively.

Even those who know, or knew, that they needed care before they entered, will STILL react negatively because they will STILL be confused, in a different place.

Their confusion cannot resolve UNTIL they become accustomed to the structure and routine of their new surroundings.

It will be harder for you than for him, but you MUST TRY to back off and let him adjust to relating to his care staff.

Answer the phone ONCE or TWICE a day, tell him you love him dearly and you’ll see him soon, then HANG UP. If he’s using his own phone, let the batteries run out and tell him you don’t know how to recharge them.

I was able to learn all this because I was caring for TWO dependent people when my LO entered a fine residence a couple miles from my house. Before COVID we never missed visits every other day or so, but that was after we were sure that LO was enjoying her surroundings and becoming more relaxed. For her, it took 5 months, but to those of us who loved her, it was all for the best.

If your dad is safe and well cared for, you will hopefully be feeling more relaxed too. It will happen….if you let it. You chose the best place you could find. Let him learn that you were doing right by him.

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Spot on post Ann!

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Many people live in MC for years. You describe your Dad as physically fit, but you seem also to indicate he isn't relaxed and isn't adjusting well.
Give the adjustment period a bit of time, for sure. At least a month. Some memory care patients need the help of a mild antidepressant or other anti anxiety medication to help them adjust but you don't want something that will bring on increased falls.
No one can really give you any guess on all this; your Dad's doctors, who know him could make the best guesses and they are almost always hesitant to do so. Each patient is as individual as his or her own fingerprint.
I know there is a tendency to want to know the future. But really you are stuck in the day to day. I sure hope things go easier for your Dad soon.

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He has had a LOT going on any of the incidents could cause a decline or for him to be upset. But to have experienced the loss of his wife, and a major move I can imagine he will be "off" for a while. I would say minimum a month to adjust maybe longer.
If you can let a few of the calls go to voice mail then call him back when it is convenient for you,. If you can give him times to call that might help. then gradually decrease the number of times he can call. Let him get used to the staff and the residents rather than relying on you.

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I tell people to look at taking a parent to a nursing home as being somewhat akin to taking a kid to college. When I took my kids to college, the schools didn't want parents to contact their student for 10 days or so, so the kids could get settled and accustomed to their new surroundings. It helped cut the cord between the helicopter parents and the overly-coddled kids who had never learned to do anything for themselves.

While an elderly person is not quite a resilient as a college freshman, there is some value in not visiting every single day or talking on the phone 15 times a day to help your dad get accustomed to his new surroundings. He is safe, he is cared for, and you should take a few days off from visiting and limit the calls to one or two a day if you feel you have to talk to him. (I would call the people there to check on how he's doing, but avoid talking to him at all for those days.)

Most places recommend about a week of no visiting, so if you can bear to do that, give it a try. He needs to stop looking outward to you to provide him with a life and to look around where he is to find things to do and get to know his new neighbors and caregivers.

It may take him even more than a month to settle in, particularly because he hasn't been allowed to do it so far. Talk to the administrator at the MC and ask for him to receive a bit more attention when it comes to drawing him into the activities and ask if they'll try to keep him really busy for a few days. He won't have time to think about getting out or you coming to put an end to his misery if they can do that.

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yungstdaughter, moving is always an adjustment no matter what age we are. Example, pulling a teen out of high school because of a family move is always difficult, they hate it, they don't want to make friends, they don't like the new school, they hate the weather, they want to run away from the new house, they hate everything.

When my own Dad [my Mom had passed the previous year] moved to senior living, I never took him out to eat or to visit my home. I didn't want to disrupt the "routine" that the facility had in place. Dad had his meals in the main restaurant and he was assigned to sit with residents the facility thought they had in common. Amazing, the couple Dad sat with were from Dad's midwest home state and a town that Dad knew.

It was recommended by the facility to give Dad two weeks to settle in and after the two weeks then stop by to visit him. I did the daily visit thing after work. Then later it was every other day. Then once a week when I brought in supplies that Dad needed.

Dad and I would talk on the phone. But at night Dad would get into his time machine and go back to the 1940's, so I had to pretend it was 1940's myself and answer questions in that manner.

All in all, my Dad loved senior living.

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Greetings!

Moving is one of the top 5 most stressful occurrences in life, even if you don't have dementia. Keep that in mind when imagining a timeline. I moved my 85 yo mom from her 3,000sqft home 4 hours away, to a 1000sqft bungalow near me. She had first stage dementia at that time, and was safe and independent. It took her almost 18 months to come out of her anger, depression, complaining, whining, and resentment. Be patient. You are part of this for sure, but it is your fathers journey.

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I am moving my husband to a board-and-care home today. He has mid-stage dementia (combo of Alzheimer’s and vascular), and I’ve reached my limit after 9 years. I told him a story last night that my sister, who lives alone, had another fall, broke her wrist again, and asked me to come help her for about a week. (She actually did fall twice last summer, first breaking her left collarbone and then her right wrist!) He raised a number of questions but eventually reluctantly agreed. But a half hour later he was hopping mad and told me I can’t go (even though I’m not actually going anywhere). That was the reaction I anticipated. So this question hits home today. We’ll see how today plays out. As always the comments here are so helpful. Thank you.

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Gosh I checked into this site today and saw your question....I am placing my husband in Memory Care next Tuesday and I have had a meltdown everyday this week while driving back from the facility. Just cannot stop crying. I have him thinking I need to go away for some medical treatment and he was okay until yesterday. He has had early onset ALZ for the last 11 yrs and turns 70 this Saturday but still healthy and seems so much younger than most people in memory care which may be difficult for him.
Not sure how many days to stay away and I also am concerned about the care at ANY facility. You pay ALOT of money for these places and still have issues.
I lasted as long as I could but now he is collapsing a few times a day and has lost control of his bowels, etc...it is alot of worry. The Drs said to take him off the ALZ meds at this stage they cause more harm than good. I took him to ER for the collapsing and hospitals are a nightmare....they have no training on how to work with an ALZ patient. He kept pulling needle out and would not let them do an EKG. They did do a CT after he was strapped down and Dr said to just take him home is brain is very atrophied. That was pitiful.... I pray for you and your Dad.

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You are doing the best you can--at some point one person cannot manage a person that needs 24/7 care. You will have to work with the staff to determine what cadence of visits works well for your husband, but there is usually a settling period. This forum is very helpful, and I also recommend peeking into the spouse forums at the Alzheimer's foundation and asking the folks there as well-there's not much that those folks haven't dealt with and, like here, they are very kind. https://www.alzconnected.org/discussion.aspx?g=topics&f=2147485438

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I would expect it to take more. My mother wanted a place of her own, and so we were able to find her a dementia care oriented AL. I'd say she was late stage 4 then, probably early stage 5 now. Even with an easy move I think it took about 6 weeks before she relaxed, 3-4 months to get into a routine. Two years in, she prefers the familiarity of her 'place'. She and I go to lunch, but if I bring her to my house she's pretty much ready to go back after an hour or two. With his short term memory gone, it will take your dad a long time to be able to develop a familiarity & a routine in a new place. Everytime he does something and everywhere he looks it will seem new to him for quite a while. If you haven't deployed a fiblet to explain to him why he's there (maybe the doctor needs to run some tests, or he's there waiting for the house to be fumigated, etc) you might want to try that, and also know that it's ok not to answer every phone call. This forum, and the AD forum here are helpful: https://www.alzconnected.org/discussion.aspx?g=topics&f=151

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It is really hard to say how long this will take. He may never adjust completely. I have a friend who has been in memory care for at least 4 months and she still keeps asking to go home. She calls her mom at all hours of the day and night sometimes 25 or more times a day. I think she has forgotten my number as she doesn't call me. When I went to visit, she kept asking me if I would take her home. Sadly she will never get to come home as she has breast cancer and will most likely die there. She is only 62 and was a brillant successful woman before all this happened. You will have to turn off your phone or block his calls from time to time to get some peace. I know this is so difficult and my heart goes out to you. Hang in there.

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Visit the facility's activities director and find a geriatric therapist who can meet with him on Zoom.

Put your phone on silence during the hours you're needed elsewhere or busy.

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Things wouldn't be much better if you took him home. And where and when is home in his condition? I would decide what schedule of contact and visit is easiest for you to remain calm and responsive in the best manner. Then do that. Don't argue with him about going home. Defer the decision, "we can think about it." I remember a person would have the person start planning what to take, how to arrange it, and tell them about it the next time they visited. Said they stopped at the first suitcase. Boy, I myself would love to go home "to health, youth, autonomy" with my older husband in the same condition
, just can't figure out how to get there. You can't take him home; it is gone. He will adjust or not to his current situation, as you must to yours at that time.

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Talk to his doctor. He is experiencing anxiety. He may need some mild anti-anxiety medications to help him relax until he is adjusted to his "new home."

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yungstdaughter: Yes, do give it time indeed; perhaps a month would be fitting although you do state further down your thread that he wouldn't be happy anywhere. Perhaps you should speak with his physician.

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I think you need to talk to the Floor Nurse, the Head Nurse and the Activities Director. I believe you need to find out what they are observing. Is he unwilling to leave his room (are they trying to get him included in activities?) Does he have a caregiver who can sit with him and listen to his gripes and do something about it? Is he dissatisfied with the food?

Your Dad has indeed had a lot of changes in a short period of time. What did he do with his time before your Mom passed? Is it possible to provide some of those same activities?

Also recognize that MC has people with a wide range of capabilities. He might be higher functioning that the average person in that facility. For me, that would be very hard to adjust to. The Nurses could help provide insight into what is happening.

I feel for you.

P.S. One of the questions that you should ask the Nurses, is if they think a visit from you at this time would be helpful. Depending upon what is happening, a familiar face might be what he needs to move toward acceptance.

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There is no set timeline for everyone on how long it will take for a person to transition and acclimte to their new life in a memory care facility.
You should not answer 15 calls a day. Don't do that. Answer one or two a day. Don't visit either for a couple more weeks either.
It takes time for someone to adjust to the new environment. Some never accept it. They cry and beg for the rest of their lives to go home.
Others acclimate very well and actually thrive in the new environment. They get much needed socialization and are content. The moment their family shows up the resident takes everyone on the Magical Misery Tour. The begging to go home, the complaining, crying, gloom and doom, etc... It's like flipping a switch. This happens often.
In another couple of months you should send someone your father doesn't know to go and just observe. See what he's like around the people in the facility. Then you'll know whether or not he's really miserable there or not.
Don't move him unless you find the facility to not be up to par. He will not be be happier in a different one.

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Thank you for your response. One more question if you don't mind? (I think I may know the answer...) Am I delaying his adjustment by picking him up once a week and taking him to my home for dinner? His sisters visit him weekly and always take him out.

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My mother is home 🏡 & she says always she wants to go home..she doesn’t recognize that she is home. She wants to go back to childhood home she grew up in that my grandparents had candy store & had apartment above store. I remind her it was sold in 1968. Now it’s a dental office

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Talk with the staff about getting him involved in things throughout the day to help him adjust and keep his mind off of leaving. Talk with his doctor about anti-anxiety meds. If you are checking on him regularly, maybe his phone can be put away and a set time for calls can be arranged. For example you might pick 5pm for your call with him. Staff can give him his phone at five to call you. Do not take him out of the facility. Bring lunch to him, walk around the grounds with him, sit and watch a show with him, bring him coffee and donuts and chit chat on a saturday morning. Make his place the place to be.

What helped my mom was meeting someone. Once she befriended someone, she had someone to eat with and watch tv with. It was a game changer for her to have a friend. She forgot about the home she left, she stopped focusing on leaving the facility and our visits were better because she was happier. So my suggestion is to get him to pair up with someone. Staff can help with this. Being on the right meds helps as well.

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I moved my older sister to MC last fall, and it took a good 2-3 months for her to adapt. She used to call me 5-10 times a day at all hours of the day and night. I told her I could not answer the phone every time she called. I blocked her number at night so I could get some sleep and unblocked her number during the day. Now she calls 1-2 times a day which I can handle. The good thing is I know she has caregivers 24/7 and she cannot wander. The MC staff will call me if anything happens. Even though she has adapted well, she still calls me sometimes asking me to get her out of there. I tell her finding another place takes time, and we can discuss it later. I'm not sure she will ever stop asking until the disease progresses because at this point she thinks she can manage on her own.

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Typically how long will transition take after move to MC?

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