Husband developing memory issues

Posted by jannew @jannew, 3 days ago

Hello everyone, I am new to this site as I look for some information, advice, and support with my husband's changing memory issues. I have read many of the posts and appreciate the sharing of stories and the compassionate help provided. This may be quite long, but here goes!
My husband is 76, I am 74. Over the past three to four years, I have noticed his occasional unusual memory lapses, which I had hoped was normal, age related memory loss, though I was concerned. For instance, we have walked our dogs on the same daily route for many years, and several trees were cut down around the corner from us. We love trees and were sorry to see them go. A week later, I commented on how I missed the trees, and he said there had been no trees there. This was a very different kind of forgetfulness in that he simply had no concept of there ever having been trees there before. Life moves on, and occasional things happened, like forgotten conversations. But in recent weeks these incidences have become rapidly more common, almost daily, and my husband gets frustrated and angry with me as I try to figure out what is going on. A few days ago, he told me "Hannah's car is parked outside". I said " who's Hannah?" (we don't know a Hannah). I looked puzzled and after a few back and forth questions and answers, as he got increasingly frustrated with me, I realized he was talking about our neighbor Rachel, who we know well, socialize with, and talk to often during the week. When I asked if he meant Rachel, he looked confused and said, yes, it is Rachel...who's Hannah? Also I'm now regularly seeing forgotten conversations about anything from casual to important, forgotten by the next day.
I was able by chance to talk alone with his PCP, who was subbing for my PCP for a check up I was having. He asked if I wanted to get my husband in for testing, but I'm not sure if we are there yet. For one thing, he denies that has memory issues, and insists that I am wrong. It is also the case that this is not all the time, and he frequently has a better memory than I do. Some days are fine. But I don't forget conversations or the names of people in our close circle, or to get the chickens in at night, which he has done for 30 years.
I am feeling anxious and with a sense of dread as things are quickly changing. I have a lot of lifetime experience with dementia.
My grandma and mother-in-law both developed dementia and both suffered for 15+ years. I was not the primary caregiver but the daughter of one and daughter-in-law of the other, and was a support, shoulder to lean on, and compassionate listener for most of my 20's and 30's, and then my 50's and 60's. My husband was primarily responsible for his mother's care for the last years, although she was not living in our home. Both ladies followed a similar path, becoming verbally abusive and physically aggressive and violent, to the extent of causing injury to family, caregivers, and other residents in memory care. It was indescribably hard. And I know you will know this.
My support is limited, our few remaining friends are older than we are and are having significant health, and beginning memory issues of their own. They need our help. We are emotionally close to our daughter but she is 400 miles away with a new baby, and I know this is not her burden to bear. I know I need to learn to accept what is happening, but the realization is only just hitting me, and based on my past experiences I am feeling stressed and terrified.
So that is my story. Thank you for reading and listening. I so appreciate that you are here.

J.

Interested in more discussions like this? Go to the Caregivers: Dementia Support Group.

Profile picture for kjc48 @kjc48

@lkbous @jannew
I welcome you too, as a newcomer to this group. I too didn't know what to do with my husband who wasn't remembering things, his refusal to see any doctor, his strange quirky ways for the last year, one day miraculously okay, the next, not so good. So, I wrote a note in the portal to our primary care in August 2025 and told her the things he was doing and my concern. And that I was worried that what he was experiencing wasn't age related. She set up an appointment with the nurse practitioner to see us both, and I told him that we were both going to the doctors', to make sure we were okay. When we got there, I had practiced all night what I was going to say, so I didn't make him angry....I remember writing it down.....we both had been under a lot of stress, that both of us were forgetting things from time to time, possibly due to all that stress, maybe the load of having to move out of our house for mold and living out of boxes, etc. That nothing felt normal now. I remember looking at him, and telling him that I loved him, that I never wanted anything to happen to him, and that if anything was wrong, we owed it to each other to help each other, why we were sitting at the doctor's that day.
I looked at my husband and told him that I loved him, that I was genuinely worried, that I did notice a change in him, and that I wanted to catch it early. So, they did blood work on me, and told him, that it wasn't unusual for patients his age, to forget, but that they were going to do a test to determine if there might be more there. She told him, if there was more there, it was good that he came in, because the earlier the findings, the earlier the doctor could address things. After that doctor tested him, told him he showed some memory issues (but mild), and not unusual for his age, but that she wanted him to see a neurologist for further testing.
So we walked downstairs and booked an appointment that same day with a neurologist. Since then, the doctor did the testing, diagnosed Mild Cognitive Impairment, and one month later he started the lequembe infusions. He's had 4 of them to date. He now tells our adult children that the infusions are important because they are going to remove his plaques. He's positive even over his MRI yesterday reading all the medical terms yet telling me he was fine. So, we're hopeful. Although I go in and out of naturally being frightened and feeling so alone. I know one thing: I'm so glad I had the courage that day to write the doctor in the portal. I hope this helps as to the timing on when to reach out to a doctor. The sooner you know as a spouse that something isn't right with your loved one, is the time, I think, we do something to slow any progression down. I hope this helps.

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@kjc48 ,wow, what a great story! So glad things are going so well! I sure do hope the meds help! Many warm wishes your way!

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Profile picture for celia16 @celia16

@kjc48 ,wow, what a great story! So glad things are going so well! I sure do hope the meds help! Many warm wishes your way!

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@celia16 Thank you for your "Wow, what a great story." The high we get as caregivers when we see supportive kudos from others. I hope the meds help too.......I really do. I keep asking him if he's okay, because I hate the thought of those infusions...but, if it helps him, infusions it is!
My best to you.........

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Profile picture for dig2dye2 @dig2dye2

There is a long list of medications that can cause this. My husband has MCI, but one new prescription sent him straight to Lewy Body Dementia symptoms. It was a horrible period in our lives because it was so sudden. His sleep neurologist figured it out and helped me wean him off the drug. Within days he was back to baseline.

I then weaned him off of other unnecessary prescriptions. His PCP supported me on that project.

Has your husband started any new prescriptions? I would go to an appointment for this reason alone.

He may not like it, my husband was very vocal about letting everyone know there is nothing wrong with him and he just was there because his wife insisted! But you do need to know and plan.

It’s so hard getting older!

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@dig2dye2
Thank you for your reply, it felt like a breath of relief to hear from many of you on the forum and know I am not alone. Your mention of the medication issue gives me pause as he did start a new blood pressure med, Atenolol, a few months ago. Looked it up and it does seem that it can cause memory problems in some people. I need to find the right time to talk with him about this, he does not think he is forgetful and thinks it is me who is having the problem. But we do need to know. Thank you for the wise words, J.

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Profile picture for tracidw @tracidw

So sorry you are going through this. I agree with several others, early diagnosis helps to rule out other issues that could be showing up as dementia.

As far as the emotions, they are tough, real and valid. All of them. It helps being able to share - helps you to express and helps others. You are not alone.

Hoping you are able to find just the right window to talk to your husband when he is most receptive.

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@tracidw
Thank you for your reply, it was a breath of relief to hear from several people on the forum, and to feel like I am not alone. I think getting into the dr. early is the clear message, the challenge will be how to do that as he thinks he has no memory problems. He does not remember what he forgets! Finding the right window will be important and I feel I need just a short time to get a bit more of a measure on this so we have a few more examples to base it on. But yes, it feels pressing to start trying to find the reasons for these changes. Thank you for the support and wise words, J.

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Profile picture for judimahoney @judimahoney

Hi J:
I get the dread and anxiety, it's stressful. The best defense I guess is education, and sounds like you have experience, and getting support (even if virtual).
Not much advice, I just get it, too and wanted to offer a virtual hug. 🫂

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@judimahoney
Thank you Judi, virtual hug and kind words much appreciated. The replies I got from the forum have been a breath of relief just to know I am not alone. I feel very supported, hugs back to you, J.

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Profile picture for kjc48 @kjc48

@lkbous @jannew
I welcome you too, as a newcomer to this group. I too didn't know what to do with my husband who wasn't remembering things, his refusal to see any doctor, his strange quirky ways for the last year, one day miraculously okay, the next, not so good. So, I wrote a note in the portal to our primary care in August 2025 and told her the things he was doing and my concern. And that I was worried that what he was experiencing wasn't age related. She set up an appointment with the nurse practitioner to see us both, and I told him that we were both going to the doctors', to make sure we were okay. When we got there, I had practiced all night what I was going to say, so I didn't make him angry....I remember writing it down.....we both had been under a lot of stress, that both of us were forgetting things from time to time, possibly due to all that stress, maybe the load of having to move out of our house for mold and living out of boxes, etc. That nothing felt normal now. I remember looking at him, and telling him that I loved him, that I never wanted anything to happen to him, and that if anything was wrong, we owed it to each other to help each other, why we were sitting at the doctor's that day.
I looked at my husband and told him that I loved him, that I was genuinely worried, that I did notice a change in him, and that I wanted to catch it early. So, they did blood work on me, and told him, that it wasn't unusual for patients his age, to forget, but that they were going to do a test to determine if there might be more there. She told him, if there was more there, it was good that he came in, because the earlier the findings, the earlier the doctor could address things. After that doctor tested him, told him he showed some memory issues (but mild), and not unusual for his age, but that she wanted him to see a neurologist for further testing.
So we walked downstairs and booked an appointment that same day with a neurologist. Since then, the doctor did the testing, diagnosed Mild Cognitive Impairment, and one month later he started the lequembe infusions. He's had 4 of them to date. He now tells our adult children that the infusions are important because they are going to remove his plaques. He's positive even over his MRI yesterday reading all the medical terms yet telling me he was fine. So, we're hopeful. Although I go in and out of naturally being frightened and feeling so alone. I know one thing: I'm so glad I had the courage that day to write the doctor in the portal. I hope this helps as to the timing on when to reach out to a doctor. The sooner you know as a spouse that something isn't right with your loved one, is the time, I think, we do something to slow any progression down. I hope this helps.

Jump to this post

@kjc48
Thank you for your reply to my post, it was a breath of relief to hear from many on the forum and know that I am not alone. Your very detailed message about the process you used to get your husband in to the dr. was so helpful. I will have to find the right approach, my husband does not think he has memory issues and thinks I have the memory issues because I am remembering things differently from him. However I really get the message that acting early is key and the sooner the better. Thank you for your wise words, and best wishes to you and your husband, J.

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It really is a personal thing and everyone has to decide what feels right for their situation. I’ll just add that that with cognitive issues, people usually don’t acknowledge they have a problem. Reasoning, convincing, etc, doesn’t usually work.

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Profile picture for jannew @jannew

@kjc48
Thank you for your reply to my post, it was a breath of relief to hear from many on the forum and know that I am not alone. Your very detailed message about the process you used to get your husband in to the dr. was so helpful. I will have to find the right approach, my husband does not think he has memory issues and thinks I have the memory issues because I am remembering things differently from him. However I really get the message that acting early is key and the sooner the better. Thank you for your wise words, and best wishes to you and your husband, J.

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@jannew
When I had a problem years back with communicating with my adult son, I remember him always trying to project back on me, like it was my problem. Loved ones in denial do that. Why, we need to go figure out the way to just get him into the doctor, even if you're doing it, under the guise of both of you getting tested, since he thinks you have the problem, etc. That's actually how I did it. Once in, the rest will fall in place. I remember when we came back from the neurologist, who tested him, and he tripped up, identifying three words: "apple, river, pear." Every morning now, we make a joke of it, and he certainly remembers now those words.....So at least we moved onto the stage of both realizing we're trying to fix a problem. I just purchased a book from Mayo " on, "Mayo Clinic on Alzheimer's Disease and other dementias", to help better understand the disease, the importance of sleep, hearing, social engagement, and diet as I read that a Mediterranean Diet may help people with this progressive disease. So I'm trying to get as much information as I can. You can order the book from Mayo. I think it was $32.00. I'm sure we'll be talking again through Mayo Connect. My best to every caregiver every day......

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Profile picture for jannew @jannew

@dig2dye2
Thank you for your reply, it felt like a breath of relief to hear from many of you on the forum and know I am not alone. Your mention of the medication issue gives me pause as he did start a new blood pressure med, Atenolol, a few months ago. Looked it up and it does seem that it can cause memory problems in some people. I need to find the right time to talk with him about this, he does not think he is forgetful and thinks it is me who is having the problem. But we do need to know. Thank you for the wise words, J.

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@jannew I am hopeful it is just the meds! When I was able to blame the medication for his problem, it made the talk much easier. Let us know what happens. Hoping for the best for both of you.

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Profile picture for jannew @jannew

@tracidw
Thank you for your reply, it was a breath of relief to hear from several people on the forum, and to feel like I am not alone. I think getting into the dr. early is the clear message, the challenge will be how to do that as he thinks he has no memory problems. He does not remember what he forgets! Finding the right window will be important and I feel I need just a short time to get a bit more of a measure on this so we have a few more examples to base it on. But yes, it feels pressing to start trying to find the reasons for these changes. Thank you for the support and wise words, J.

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@jannew One thing that helped me with Mom, I would frame things in terms of myself. "It would help me and give me some relief if you'd get checked out by a doctor." Also, I said there were different medications now that worked best if something is caught early.

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