Husband doesn't recognize me: Struggling to keep him safe

Posted by sr5367sh @sr5367sh, Dec 16, 2025

I've been lurking here for quite a while, just reading posts and gathering information. I am literally in tears on a daily basis as his dementia symptoms seem to just progress and multiply every day. He is diabetic with hypertension and Stage 3a CKD. All of these issues were being well managed and under control for the past 8 years.
About 3 years ago, my darling man began getting lost while driving familiar places, misunderstanding words, and occasionally mis-speaking, calling everything a whatchamacallit or people whatshisname. As it began happening more frequently, I spoke to the doctor about it. He denied any difficulties and put it down to being 73 years old. Our PCP said to keep an eye out for changes and report back as necessary. At this point, we were doing 6 months check-up and all was relatively well, including his blood work.
This past April he began having a problem using the TV remote control. Then he started getting dressed and going to church on random days of the week. Doctor advised him to stop driving, but he refuses. Extremely belligerent and verbally aggressive when anyone mentions it, especially the safety of himself and others.
I fo all housekeeping and financial tasks because he can't remember how to use microwave or stove or washing machine or any electronics, including his cellphone at times.
He uses a catheter because he has a hypotonic bladder. Last week he asked me what these things were for. I told him they are for urinating and he asked me to show him how to use it. Yesterday he said he can't remember how to do it, so I do that every 4 hours now.
On Sunday he got up at 4am, packed some shirts and told me that he was leaving and going home. He refused to believe he lives here and that I'm his wife.
He said his wife has been gone 3 days and he's not staying here. I persuaded him to stay and just wait for her to come back, that she may have had an emergency or something happened with her family out of town, but he's really upset that she would just up and leave him.
I've been here with him, all day, every day, but he just thinks I'm some woman taking care of him until she returns.
This not knowing who I was happened previously about a month ago for about a week, then one day he asked me a question using my name, and I said, You know who I am? He said, Of course I do, you're my wife. Why are you asking me that?
So all seemed well until Saturday night when he said Sheila put my socks away and I don't have any clean socks. I just looked at him and got the clean socks. Since then, he keeps asking where she is and when she will be back. All of his other conversations and behaviors are for the most part, our new normal.
I am just at a loss as to what to do that would be most helpful and to cause him the least amount of agitation and distress.
We live alone, but he does have adult children who have been less than helpful in the oadt, and actually cause him to be more agitated and distressed.
We have an appointment with his PCP on Monday, but I'm really struggling here to keep him safely indoors until then.
Any suggestions would be greatly appreciated.

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Profile picture for celia16 @celia16

@sr5367sh , Ref. Your update. That’s a lot to manage. So glad you have outside help coming in! That’s great! I hope it helps you and him.

I’ll just say that with the meds for agitation….often it’s a risk/benefit analysis with the understanding that risks exist but staying in the home is often a primary goal and the ability to do that depends on reducing the agitation. I might seek input from a doctor who regularly treats patients in that situation. My dad’s heart rate was low too, but he needed certain meds to treat his mental distress. He had afib and congestive heart failure. He was not a candidate for pace maker either. He eventually came off BP meds due to low BP.

Depending on his condition, he may become to need skilled nursing care. You don’t have to be bed bound. They provide care for people who have dementia too. It can be quite subjective.

I’m not sure which state you are in, but in most…qualifying for financial help for Memory Care is different than a nursing home. Memory Care help is based on state assistance programs (in my state called Special Assistance) and has strict often low income limits. So it’s easy to not qualify if you make too much. But nursing homes are funded differently by Medicaid and that’s a different formula. It can be easier to qualify and various factors are considered. Not the limits for Memory Care. It’s very complicated, but I’d explore it with an expert in advance so you know what to expect. An estate planning attorney who focuses on Medicaid might be helpful.

Good luck with everything. I wish you and your husband all the best.

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@celia16 Thanks for your suggestions. We're in Tennessee and I just found a resource called Senior Helpers that is supposed to help caregivers navigate this process. I'll be calling them tomorrow.

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Profile picture for sr5367sh @sr5367sh

@memoriestomoments
Thank you so much for your helpful suggestions. A few things have changed for us since my initial post. After a 5 day hospital stay following a UTI, we are now receiving home care services put in place with the help of the hospital social worker. He had an episode in the ER and had to be sedated and restrained. Thankfully he was seen by a neurologist who recognized many Lewy Body Dementia symptoms and was able to direct his treatment process so that he received more appropriate care.
He was also diagnosed with bradycardia, which unfortunately eliminated the medications he could receive that would have helped to reduce the agitation and hallucinations. All of those medications have the risky side effect of lowering the heart rate, and his heart rate is currently averaging between 39 and 45.
The cardiologist will not consider a pacemaker because the effects of anesthesia on patients with advanced dementia does not improve quality of life. If he made it through the surgery, he would most likely end up in ICU, then most likely a nursing home. So, here we are; caught between a rock and a hard place.
We don't have long term care insurance and the cost of a good memory care facility is beyond our means. We're both receiving pensions and Social security benefits, so we're not eligible for Medicaid services. If anyone has any information regarding any help or services that would help with at home care, I would be forever grateful if you would comment.
His Medicare plan is paying for a physical therapist, occupational therapist, a speech therapist and a nurse who makes home visits. The VA has provided a sitter who comes for 12 hours a week to give me a break so I can take a nap or run errands or do nothing at all. They also provide Depends, so that is another huge benefit I am happy to receive. I have to catheterize him every 4 hours, but thankfully Medicare pays for them.
I'm still physically able at 69, and my husband, 74, is still fairly ambulatory but using a cane now for balance issues. In spite of what seems like a mountain of issues, I do hope that he can remain at home for however much time we have together. I'm trusting in God to see us through.

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@sr5367sh
Hello:
I was under the impression the VA had facilities where he could stay at no charge, if he's a Veteran?
My mother-in-law placed her husband in a VA memory care facility when his Alzheimers became more than she could deal with over time. She did have to wait a few months for a bed to open up for him there.
Good luck to you.

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Profile picture for judimahoney @judimahoney

@sr5367sh
Hello:
I was under the impression the VA had facilities where he could stay at no charge, if he's a Veteran?
My mother-in-law placed her husband in a VA memory care facility when his Alzheimers became more than she could deal with over time. She did have to wait a few months for a bed to open up for him there.
Good luck to you.

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@judimahoney Yes, the VA does help veterans with medical care and other services, but some services have eligibility ratings based on whether or not the veteran has a service connected disability and family income. Unfortunately, (fortunately?) my husband doesn't have a service connected disability and our household income is above their maximum limits.

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not sure what state you are in but in some states the MD can write a letter to the motor vehicle department to say it is unsafe for him to drive (and it takes the blame off you).
i’d suggest making an appointment with a neurologist for an evaluation of his condition (our PCPs were not capable of the evaluation.)
talk to a lawyer about the risk of him driving and what needs to be done for estate planning.

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