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I'm 73 and in good health. My wife of nearly 50 years is 68. Eleven years ago, her right leg was amputated above the knee after several failed knee replacements. She wasn't able to use a prosthetic leg, but mastered her electric wheelchair-- to the point that I almost forget she only has one leg.
Her behavior became altered around the first of June, and she now has full-blown dementia (still in the process of being evaluated as to cause, type, and treatment). She still knows people and pets, but is totally disoriented as to time and place, and while her demeanor is usually calm and sweet, she can suddenly go bat-shit crazy-- not violent, just agitated. For instance, the SNF called me tonight to calm her down-- she thought her pills were poison and that the caregivers were trying to harm her.
She can no longer use the electric wheelchair, and has lost the ability to transfer independently-- she can use a slide board with assistance, or a Hoyer lift. She has also become incontinent.
After 12 days in the hospital due to a fall, she's presently in an SNF for rehab. She'll be leaving the SNF within the next couple of months-- and I'm trying to decide what comes next. I've visited a couple of top notch Memory Care facilities, but as good as they are, I still came away feeling like she'd simply be warehoused there. She is far more alert and active than anyone I saw in those facilities.
We have no children or relatives nearby, and most of our friends live far away. But, we have a single-story home that would be easily adaptable for use of a Hoyer lift and anything else we might need. We also have the resources to hire a caregiver for up to 8 hours a day.
Is it feasible to think I could care for her at home?

There was a gentleman in my mother's nursing home that was younger than almost everyone else there, but he was a big man in a motorized wheelchair and his wife couldn't handle the physical side of his care any more. They had an accessible van and she was able to take him out most days - I have no idea where they went or what they did. My point is it doesn't have no be all or nothing, you can play things by ear and let the facility handle the bad days.
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Reply to cwillie
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I vote for the memory care.
You say she will be warehoused there. The sad truth is that she will be sent there because she needs 24/7 INTENSIVE care by a team of workers. And that team doesn't exist in your home and you cannot be that team. That team exists in what you call a warehouse. And they likely often feel the SAME as you do about what happens when we lose everything including our mobility and our continence and any sense of reality and how to live in it.

This is a simple (if devastating) fact. You cannot do this. You didn't cause it. And you can't fix it. And that is the sad truth of it all. It could conceivably kill you, and then where would you dear wife be.

The time for evaluation and diagnosis is now, while she is in care. The time for placement is NOW while she is in a place where there is discharge planning. Start by seeing an elder law attorney NOW, soon as you can, about finances and division of finances looking to placement.

There is what we want, what we dream could be, and then there's reality. I am afraid you are smack dab in the latter. I so wish you luck, but you can only do so much. You are human, not a Saint. And the job description for Sainthood is not a good one.
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Reply to AlvaDeer
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Your wife should go to a facility where they have the aides, resources and knowledge to care for her properly. Taking care of such a patient at home always sounds great - you think you can handle it - but it deteriorates rapidly. When she goes B/S crazy, as you call it, good luck with getting the aides to stay. Then you're always looking for new ones. Then you're shorthanded some morning and you're trying to get her bathed but she goes B/S crazy again. You might be focused on having your morning coffee with your wife in an ideal home scene, but your home will no longer seem like a home with Hoyer lifts, tub seats, loads of Depends to dispose of when they won't fit in the trash can, loads of Depends to get delivered, bundles of laundry for you to do, and nights when she's crying or yelling for help and falling out of bed in the process. The smells and mess of care at home can be overwhelming.

Let her be cared for by professionals, and you take care of yourself. You can advocate and be supportive from your peaceful home.

Oh, and I've done home care and am doing it now. Nuh-uh. Not a good idea.
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Reply to Fawnby
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My advice is be open to both, and watch the balance. Certainly give it your best effort at home, it’s what most of us would want. Nothing wrong with making reasonable home modifications and hiring help to hopefully provide care there. Be aware of your own continued health, physical and emotional, get out of the house, do activities you enjoy, have a social life at least to some extent. Watch the finances for your own future. If it proves to not work or be too hard or unsafe, then you’ll know you did your best and it’s time for managed care. Your wife is blessed to have you
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Reply to Daughterof1930
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One thing I should note: I have Wyze cameras in her room at the SNF, so I see and hear everything that goes on there. 90% of the time, it's just her sitting in bed or in a wheelchair. Caregivers come and go, they feed her, change her, give her meds, etc. She usually engages them in conversation, just as she would before dementia. But the truth is, the caregivers aren't doing anything I (or home aides) couldn't do at home.

I think my problem is that she is sometimes entirely lucid--she called a few minutes ago, discussed how therapy went, and asked me to bring over KFC for dinner. You'd never know that twelve hours earlier she was totally out of control, refusing meds, insisting she was being kept in the basement of a house, etc.

I have no problem putting that crazy woman in a facility, and I'm under no illusions-- that will probably be required one day. But when she's lucid and rational for much of the time, as she is now, it seems like a huge betrayal. When the time comes that she doesn't recognize me and doesn't know where she is anyway, I think I'll feel differently.
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Reply to flibmeister
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Seems like she's more of a candidate for LTC and not MC? I'm only mentioning this because there might be more "with it" people in that wing, plus Medicaid can cover the cost when she qualifies financially.

For in-home care you will need to consider the loss of your privacy every day. In a good facility there are activities and events and other people. My MIL is in an excellent LTC facility on a large metro lake. She's in a wheelchair yet they take her out on the pontoon boat to fish. They have fancy dinners at Christmas and Valentine's day, they have visiting pets and musicians, bingo, movies, raised garden beds for residents to grow things, etc. An argument against keeping your wife at home is that it will be a more "sterile" environment for her -- unless you find a spectacular aid who won't be looking at their phone every 15 minutes. Being at home may mean more to you than to her as her cognition deteriorates.

Is your wife a 1 or 2-person assist? If she can no longer transfer herself, are you willing to be locked in as the 2nd assistant? How much management are you willing to do? When that aid is sick or on vacation you will need to find subs. Plus, you are then an employer in the eyes of the IRS and need to provide a contract, do payroll withholding, quarterly reporting and W2s.

I'm not against in-home care it's just that you will need to go into it with your eyes wide open.
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Reply to Geaton777
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I can only echo everyone else here... she needs more care than you can provide at home, both for her safety and for yours.

I would just like to say that you're a loving and caring spouse, and are trying to do your best by your wife. As hard as it to do, sometimes recognizing our own limits is the most loving thing we can do. If she's receiving good care, it frees you to have your relationship without trying to be her spouse and her caregiver.
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Reply to Nepenthe
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Flib, I feel for you. I hire a caregiver company that comes in and spends 4 hours a day with my vascular dementia wife doing what you talked about. That gets me out of the house 'going to work' without a bunch of drama. That's money well spent. Plus, it gives her more people to interact with.
Have you heard the term 'sundowning'? When the sun goes down, the hallucinations and personality changes start. We fight the sundowning with a prescription med. I don't know if mentioning specific drugs here is kosher. This is my first post here in agingcare.

My wife's issues started with a stroke and blood clot during a knee replacement surgery right before the covid lockdowns. She spent a month in a rehab facility during the lockdown and was only allowed window visits. Those visits were like a Sara McLoughgin ASPCA commercial with her shaking and wild eyed alone in her room. I never want her to go through that kind of thing again. So I'm doing all I can to keep her at home. When she gets agitated and asks where she's at, I tell her 'you're at home where you're loved' and that gives her some peace. I also like to pray over her at night when I get her settled in for the night. She likes to hear my prayers and I do think it helps keep the voices in her head at bay.
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Reply to jwellsy
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Yes, Dementia does not happen overnight. Its gradual. I so hope she has had the propper scans abd Labs. I would say a bad stroke.

I suggest you see an Elder Lawyer about splitting your assets. Your wifes split would go towards her care. When almost gone, you apply for Long-term care Medicaid. Once on Medicaid, you become the Community Spouse, remain in the home, have one car and enough of your monthly income to live on.
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Reply to JoAnn29
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You’ll destroy your good health really fast trying to provide hands on care for someone so profoundly disabled. Put her in one of the nice facilities you toured and visit as often as you like.

My grandpa had lunch with my grandma in a facility literally everyday. Even brought their dog to visit most days. The other residents loved that.
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Reply to ZippyZee
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