Husband developing memory issues
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.
@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!
@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.........
@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.
@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.
@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.
@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.
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.
@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......
@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.
@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.