What were the first dementia signs you noticed?
My husband has vascular dementia as a result of at least 7 TIAs and 1 larger stroke as shown on an MRI. The only one we were aware of was a TIA in 2016. I'm guessing that some or all of the others may have happened in his sleep because there were no obvious signs like there were with the 2016 one.
Anyway, I've been thinking back to things that seemed "off" well before I started suspecting a problem. One thing was that he started mixing up pronouns. He'd refer to a female pet as "he" and vice-versa. He still does and he mostly does it with animals. He'll also tell a male pet that's he's a "good girl" and vice-versa.
When it first happened, it became a joke, but now I wonder if that was one of the first signs that something wasn't functioning the way it should. I'm curious if others can think of things that seemed "off" before the problem became obvious.
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DEAR MABLESMITH
THANK YOU SO! MUCH !!! YOUR'S IS THE BEST ENCOURAGEMENT I'VE GOTTEN SO FAR. LIVE EACH DAY! EAT HEALTHY!
I'M GOING TO CONTINUE WRITING A NOVEL I'VE BEEN WORKING ON FOREVER!!! MY PRIMARY DOCTOR HAS GIVEN ME A PRESCRIPTION FOR PHYSICAL THERAPY, AND I'M GOING TO STOP BEING FEARFUL AND GO!!! ALL THE BEST BACK TO YOU AS WEL!!!
Thank YOU!
Do you mind if I ask if you are taking the prescription drugs for the MCI? My husband is on two, one being a patch, and I honestly believe he has progressed more in the disease in the last 6 months since being on it. I really am considering stopping the meds. I ask my pharmacist his opinion since he sees so many in the similar situation and he said in some there is the hopeful delay in symptoms, in others not so much. I don’t have a lot of confidence in the doctors we are working with it’s all about the meds. This is a hard journey, but I want it to be the best for him that we can make it.
I take only one medicine for pain which is not for MCI it's for occipital neuralgia. After testing my neurologist thought I should begin meds to slow the progression so I began taking the following in this order: Memantine for memory - mind felt fuzzy; Amitriptyline - anti-depression & pain, I was neither, it made me fell out-of-it; Donepezil - this was the worse, I had nightmares & woke hollering for my husband. I never took more than one prescription at once. We tried them separately. Since there is no cure for dementia and I've been at this for less than 2 years I'm taking it a day at a time. Most would say I don't see any difference in you. I just say you don't live with me. You wouldn't believe how many times I've had to use spell check! I can't spell any more! Of course every situation is different. I have trouble with what I call "tracking". Keeping up with conversations when everyone's together or when subjects change. Even when my husband and I discuss every day things. I tell him to don't be so detailed. I could just go on and on. I won't worry as to whether this will progress. My children can see small changes in their mom but I am 80 so that's what I say. The doctors see a lot of patients and we want what's best for us and they can't always give that when we want it. My best to you. Of course I don't know if you folks are people of faith but I'll remember you in prayer. Best wishes to you. I would like to hear from you again. I won't be so detailed next time!
@elisabv2u
I am so sorry to hear of your husband’s significant decline. How old is he? I really feel for you and his loved ones having to watch the person you once knew slip away. It is like having to grieve the loss at each stage of decline.