Advice on Transition to MC
Hi. With reluctance and fear, we are going to move my Dad from independent living with my Mom into MC. I know this is a painful process for all families, My Mom and Dad have been together for 65+ years. My family is scared that my Dad will become very angry at us, especially my Mom (the dutiful wife). We don't know what lies ahead. How do we prepare? He still knows us, knows our names with lots of confusion for everything else. He sleeps most of the day, is either lying or sitting in recliner. What kind of advice do you have for how to handle the transition, 1. What do we tell him (he's going to rehab?). 2. How do we handle when he becomes upset? How do I keep my Mom from falling apart? I keep reminding her it's best for both of their safety and wellness…. Any advice appreciated.
Comments
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Hi Tootz, it's generally advised not to tell him anything before you go—perhaps that you're going someplace for lunch, then arrive (by arrangement) just a little before lunch. Then let him know he's there for rehab, and when he asks about going home you tell him when the doctor says it's ok. If you tell him up front that you're taking him to rehab, he may refuse to go.
You can also point out to Mom that she can still spend time with him, but she will be spending time as a wife and companion instead of as a caregiver. You can point out that he will be around people more and may have more things to do (although he may still spend his time sleeping in the recliner). I would plan to take Mom to lunch afterward as well, to provide some transition and company. She will be very lonely at first even if she participates in activities in IL.
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Take a deep breath. Put your hand on your heart. Breath in, exhale slowly.
I start with that because I know how hard this is, and I can also see that you have made huge strides already. You were anxious and worried and unsure. Now you have a clear plan. Stop a minute and let yourself feel proud. You are already doing this hard thing.
The MC care team and the social worker will be able to help with the transition. This is their job, after all. They will have suggestions and options, and you will make choices about what will work best for your parents.
I agree that not telling your dad in advance of the move is generally considered best. When he is in the new location, see what works: “Your doctor wants you to have some special care”; “you’ll go home when the doctor says you can”; “we’ll be visiting you a lot!”… “Mom will come see you really often!” That sort of thing. When he gets upset, rely on MC staff to help you.
And yes, your mom will need extra support. In many ways this transition is going to fall hardest on her. Maybe take her out for a meal. Bring her flowers. Reminisce with her about happy or funny times. Remind her that what she is doing requires courage and is just another way that she is caring for your dad. She is NOT “giving up”; she is making the hard choice to get him the care he needs.
We’re all in your corner.
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We moved my mom to MC last August. She is in early stage 6. She still knows us and is very conversational, but her short term memory is virtually nil. She can feed herself but needs help with all her ADLs. We told mom "the doctor wants you to stay at this special rehab place for a little while for some serious physical therapy". Since she loves PT, this went over pretty well. We went over this beforehand with the MC staff, so everyone would be on the same page. They assisted in the hand-off, and it went smoothly. Mom has no recollection that I was the person who took her into MC.
The first few weeks were rough, but nothing the MC staff hadn't seen before. (You can search for my posts about this for more details.) They added a mood stabilizer to her med regimen, and that helped a lot. After about 2 months, they were able to discontinue it. Whenever she asked when she could go home, we would tell her "when the doctor says it's ok - you won't be here forever". We would then change the subject to something more pleasant. I always bring my "bag of tricks" to every visit which include family pictures, magazines, and treats she likes.
It also helps to have the first few visits in the MC common areas where there are more distractions. For the first few visits, she thought it was the first time I'd ever been there, so we would walk around together, and she would give me a tour. Still the social butterfly, she loves introducing me to people. When we walked past an area with musical instruments, she pointed to the drums and said "that my favorite thing we do here". (Never in my life had I imagined my mom playing drums!) Walking past the piano, she'd say "people come and play beautiful music".
Now, 5 months in, she really doesn't ask when she can go home, but she sometimes asks if we can "take me to see my house". I usually say something like "Yes, but I can't do it today because (fill in the blank - I have a doctor's appointment, etc.) I don't take her out because at age 97, she is very frail and a fall risk. I'm no spring chicken either.
Mom's quality of life has improved greatly in MC. She's made friends with some of the residents, she loves the staff, and they love her. She participates in most of the activities and proudly shows me her art projects. She was always a very social person, but with progressing dementia, her life consisted mostly of walking around her AL apartment looking out the windows and overwatering her plants. She had 24/7 caregivers, some were great and engaged with her, but others mostly sat around looking at their phone.
A move is hard at any age, but it's going to be much harder for someone with dementia. Have patience in the early days.
Moving your father to MC will enable your mom to once again be your father's wife instead of having to also be his caregiver, with all the stress and strain that causes.
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You are doing the right thing! I think the key thing is don’t tell him in advance. My brother insisted we tell mom a week ahead of time and it was a mess. What you tell him should work for him. Your family knows him best. It is generally advised that visits are limited in the first few weeks after the move. You want to give him a chance to participate in activities. If family is there he is not going to join in. Once he is there for a bit you will know what activities he likes and plan visits that don’t interfere. I never visit at 2:00 since that is bingo time. I would also avoid taking him out of the building until he has had a chance to adjust. I hope it goes well.
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Good advice so far. Not everyone needs to be "left alone to adjust for few weeks", especially if you are moving both parents and one is higher functioning. Mom may feel abandoned or feel increased stress of responsibility even though staff is there to help with the transition and with general needs. Maybe you can plan visits around dad's nap time if you being there will be unproductive. You will know from interactions with them and with staff and adjust as needed, but show up in early days at least to observe how it is going.
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My mom has been in MC since Sept and is still adjusting. Honestly it has been very difficult. She doesn’t think she belongs there and is angry most of the time…and blames me mostly. She thinks I’m the decision maker and can change her situation. It bothered me a first but I’m learning that it’s the disease. I try to deflect and change the subject, which works some of the time but not all of the time. She has okay days and really, really crappy days. Surprisingly we had a lovely Christmas Day with her at MC…which I’m so thankful. She had a good day. We never know what we are walking in to at any visit. I now visit my mom twice weekly, my sister does alternative two days. We limit our visits because we’ve been taking care of her for seven years daily and it was taking a toll. You will not be able to control your parents feelings or behaviors but you can advocate for them once he is there. The other posters gave you good advice. I’m not sure how anyone can truly prepare for a parent move to MC. We have no idea how quickly they will adjust. My advice would be once he is there to have regular contact and conversations with the staff (psychiatrist, physician, nurses and activity people). My mother’s daytime charge nurse is wonderful and texts me if there’s a daily issue, update and sends us photos. The rest of the staff sees us regularly so we are comfortable speaking to them about her behaviors and needs. We bring mom special lunches and treats, maybe your mom will enjoy planning to bring a meal over to share a couple times a week. They can watch tv together and just enjoy each others company. You will need to remind yourself that this could be a long road so you don’t want to burn out thinking of everything all at once. Little steps. Reassure your mother that you are there for her and will navigate this together as a family. Sending you well wishes!
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Hi Wizmo- Thank you. There is no way that I would/could stay away. Our family all live within 5 minutes. I know my Mom who will be in the same building but living in their independent living apartment will probably go for more time than she probably should initially. UGH- This decision to move my Dad is to provide safety and health to my Mom who is withering away. However, I fear her heart will break from the separation so it's almost as if both things are very hard and we have to pick which one will be the one that literally breaks my Mom's heart… I don't say this lightly at all. I haven't considered my Mom's upcoming challenge with staying away from my Dad….. I think she believes she can stay there and should, for hours a day. :-(
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Thank you- oh thank you for sharing. We have our memory care meeting tomorrow to discuss transition and when we do the move. Your advice gives me good insight and preparation.
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Thank you for your kind words and helpful tips. I am grateful for this community
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Commonly Used Abbreviations
DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
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