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Moving to a new home

Good morning, my hubby was recently diagnosed with Moderate stage Alzheimer's. We had planned to downsize our home next spring. Now that we know his diagnosis, what has been your experience in moving at this stage? I am worried he won't think our new home is home and he will always be looking to go home. Is it best to just stay pout if we can mange the property? Am I over thinking this?

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  • H1235
    H1235 Member Posts: 1,164
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    Welcome. What struck me is you said if “we” can manage the property. He may be able to help for a bit, but it’s really going to fall on you. Can you manage the property. I would consider safety concerns. Does your current home have lots of steps, is your bedroom and bathroom on the main floor, is the home located close to family that may help, is it a high maintenance home with a huge yard, is the bathroom setup good? You may also want to consider the financial aspect of the move. Dementia can be very expensive if memory care is eventually required. Would a smaller home leave more money for that situation? You have so much to consider. I’m sorry you need to be here. I attacked a couple of general resources I found helpful.

  • midge333
    midge333 Member Posts: 570
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    We downsized and moved about 4 years after my DW's diagnosis. My DW did well with the move and I have no regrets.

  • JulietteBee
    JulietteBee Member Posts: 222
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    I am an only child with one remaining parent. I had my DM downsize last fall, prior to her official diagnosis as I had been seeing evidence of dementia emerging over the past 3-5 years. She left a 2100 sqft house for a 900 sqft IL apartment.

    The move was extremely difficult because she could not stay focused. I did not live with her, so daily she was given boxes and told to focus ONLY on her clothes and her file cabinet.

    Daily, I would go over and find nothing was done or she was crying while packing up other areas she was not tasked with doing. She stated that she didn't remember me telling her to focus only on those 2 areas.

    She was of ZERO help and was probably at a stage 4/5.

    I am dealing with my own terminal condition but literally had 6 weeks shaved off my life as the move was done all by me & mine. The "movers" were my hubby and adult child. The packing and unpacking was done all by me, while mom sobbed daily.

    If your move is NOT financially necessary, I'd suggest you guys age in place & pay to get help to come to you...imo😢

  • JJ401
    JJ401 Member Posts: 369
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     "I am worried he won't think our new home is home and he will always be looking to go home."

    Staying in your current home is not a guarantee that a loved one won't ask to go home. It happens with people who have lived in the same place for decades. Even people who still live in their childhood home can ask this. Asking to go home is not usually a request for a specific place, but a plea for a feeling of safety they felt in childhood.

    If you planed to downsize, do it. You need to consider the needs of both of you. If you plan to keep him home (as long as you can), think about bedroom location, bathroom accessibility, outside accessibility, etc. Consider what you can handle doing. Do what is best for both of you.

  • WIGO23
    WIGO23 Member Posts: 202
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    We moved fifteen months ago to be near our daughter and son in law after DH ALZ diagnosis. I can only speak to our experience. We both feel like we’d like to go home! Leaving a city, friends and my brother after 72 years has been very, very difficult regardless of the reason. We have no friends here. It has been hard to find a new doctor as good as the one we had for years. And just the change in familiar places and routines is challenging. The help we do get from family isn’t enough to overcome the sense of loss of home for us. We did our best to make a good decision but our enduring sense of loss is very sad. Will we ever adjust? Who knows?

  • Timmyd
    Timmyd Member Posts: 186
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    Just an observation. I see two different conditions being described.

    1. down sizing but staying within the same general area
    2. relocating to a new, less familiar area.

    Number 1 seems like less of a risk than number 2.

  • CindyBum
    CindyBum Member Posts: 502
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    edited September 4

    We moved to a small, remote town at the recommendation of our doctor. All that peace and beach walks was supposed to help what the doc was still calling MCI. It made no damn difference on that front. We have worse healthcare options, but I'd still do it because I absolutely love living here. I'm not sure what I'd do without the beach walks, even though my DW can barely manage them anymore. Turns out, the quiet was for me instead and I'll take it!

    I will say this. My moving experience was pretty awful. My DW got incredibly overwhelmed by it and was still in her apathetic stage. I had to do it all and it was hard, hard, hard. So, plan for that eventuality. I should have just hired people to back us up and move us. Sure I saved money, but it nearly killed me.

    And, H1235 is correct. You will lose your hubby's help managing the house and property sooner than you think. Personally, I'd downsize now, but I say this a lot….your gut knows. Trust it.

  • sandwichone123
    sandwichone123 Member Posts: 1,050
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    Choose for you. Your spouse may or may not like the new place or the old one, and may or may not see either one as home after a while. Regardless of what your plans are there is no way to tell how long he will be living at home in any case. Wherever you are happy you will be able to provide the best care, and you are the person that will be living there when he is no longer with you.

    If you choose to move, hire as much help as you can afford, because he will not be able to help and may spend significant time "helping" by undoing whatever you spent the entire morning working on. The more you can get done by someone else, the more calm and patient you can be throughout the move.

  • harshedbuzz
    harshedbuzz Member Posts: 5,656
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    @P120481

    Hi and welcome. I am sorry for your reason to be here but pleased you found this place.

    I am not a spouse of a PWD, but I did move my parents when dad was in the moderate stages of the disease. I did both kinds of moves— long distance to be nearer family and then from an apartment to a home in a 55+ Active (as opposed to CCRC which would have been my first choice) community. If you add up dad's move from his place in FL to the one in MD in July, from which we took him to the ER in August which sent him to rehab for 5 weeks for September, to the apartment which was meant to be temporary in October before finally landing in their downsized house in January we moved him 6 times and I learned a lot on the way.

    My advice would be to pick the place where you want to be in Stage 8.

    If you love your house and you can make late-stage caregiving work by adding a full bath with walk-in shower, converting the living room to a bedroom, and hiring lawn care and other maintenance, stay there. The caveats would be that sometimes hiring people to do tasks the PWD thinks they can do can cause agitation. Other factors to consider— the availability of home health aides and day programs in the area. Some folks who live in very rural or as well as the value of your home if there is a potential for you to need Institutional Medicaid to pay for care in a facility at some point.

    If you want a smaller and easier place to manage, do that. As the disease progresses, "home" becomes more of a feeling of security and less confusion than an actual building. Many who ask to go home seem to mean the time and place when they were young kids.

    Things I learned doing this for my parents:

    Do not involve a PWD in the process. I've done it both ways, trust me on this. PWD don't recognize their deficits and lack the executive function to be logical. Decision-making is stressful for them. Sometimes they make a decision and then renege on it the next day. Sometimes they make decisions that are counter to their needs for instance, when mom decided they wanted to buy a house dad made noises about buying an old Victorian that had been converted to apartments and becoming a landlord.

    Things went best when we did everything behind dad's back so he wasn't subjected to mess and drama of the moves. He was in rehab when we moved them to the apartment. and when mom took possession of new home, I sent them to a nice hotel for the weekend while I and my minions (professional movers, DS and niece) got the house turn-key ready.

    Because mom downsized from 2x 2000sqft homes into a 1500 sqft, some things were given away but for a time we stored them in a storage unit. I took pictures of the interior and whenever dad would accuse me to stealing his things, I could show him the pictures and explain they were in storage.

    If possible, I would move into the new place, and then stage and sell once you're out of the house it possible. You might want to talk to a CELA about titling the house; mom's CELA insisted she put it in her name only. As POA I physically managed the settlements of both their old homes and oversaw the moving of the furniture, cars, etc.

    Good luck.
    HB

  • mrahope
    mrahope Member Posts: 565
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    We moved when my DH was in the middle stages. He was not happy about it, but recognized that it would be good to move near DS and his family. My DS pushed for this when he saw how hard it was for me to get my DH up the stairs and out of our townhouse during one of his illnesses. It was the right thing to do. DH did have moments of wanting to "go home" but to him this meant the foreign country half a world away where he grew up. In fact, before he went to MC, he had literally packed all his belongings and tried to take an Uber to the airport, some 30 miles away. Home, as others have stated, is a concept rather than a place.

    As for me, I'm still happy we made the move, even though DH no longer lives here. I'm near the grandkids and over these two years have begun to find friends and connections in the new place. It takes work to make oneself at home in a new town, but it's worth it. YMMV

  • persevere
    persevere Member Posts: 14
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    Caring for my DW who was diagnosed in 2019. About a year and half ago I went through this decision process because we have kids living in jacksonville about 300 miles away. I was also retiring at the time (early) to care for my wife. Basically went through a nervous breakdown trying to sort through all this as we've been in our home in a small quiet town for 35 years. We finally settled on getting and apartment near one of our daughters and keeping the house since it's paid for. At first, it was nice and cozy and we were close to the kids. But it didn't take long for the big city to grind on me, and the kids have their own lives so the help I thought I would get really didn't materialize. And the grandkids, as much as we love them, have their own lives too. At the end of the day we are spending more time back at home and the apartment is empty and an anchor around my neck. And the wife doesn't know the difference to be honest. It's all about YOU and what works for YOU. You are the caretaker. It's taken me a while but that's the deal.

  • Iris L.
    Iris L. Member Posts: 4,911
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    Regarding expecting PWD to help with downsizing and moving:

    • PWD can no longer make decisions. They can no longer decide what to keep. They can no longer organize. They lose things.

    • PWD can no longer execute tasks. Even if you give clear instruction on how to do something, they cannot perform any but the simplest one-step task.

    • PWD are easily frustrated when then can no longer complete tasks that they used to do. PWD should be prevented from frustration as much as possible by giving them failure-free tasks and activities to do. This will help keep the caregiver from a lot of frustration also.

    I hope these insights help someone.

    Iris

  • Anna2022
    Anna2022 Member Posts: 236
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    We were planning on moving a few years ago but DH could never decide where he wanted to go (I had specific criteria but his criteria never quite solidified) … it turned out that indecision and re-visiting the subject over and over without a decision were early signs of DH's impending dementia. But if I were to think about moving now, the move would be for me, where I want to be and where I'd like to live when we arrive at Stage 8. As others have said, the concept of "home" becomes a feeling not a place.

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
Read more