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Yes MCI has many similarities and differences as we are learning. I take 1 day at a time. And I try to keep him as happy as I can. I do things for myself too, like work part time, bicycle, rebounding and lots of proper breathing to help with my own stres, and I speak to a therapist every 3 weeks for talk therapy. I try to get some piano playing in as he likes to hear it. And he likes opera and oldies. He and I live alone in the home but our kids stay in touch as they are aware. We visit grand kids like 4x a week for an hour or so. I’m hoping he can stay where he is with MCI because all of these consistent things plus family, eating clean food, taking brain supplements is important.
Don’t know if you follow Brain Doctor who gives tips on reducing the effects of MCI, Alzheimer’s and dimentia but he is great. He has a practice too.
He’s on Facebook, IG and Tic Tok. Plus I am taking his Brain Supplements for myself too. Check him out - Dr Clint Steele. Enjoy your day!
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You've figured out how to keep active; I feel like it's just my husband and I but we had a crisis in our house from the AC, had to move out, had to move everythign out, and we're in a rental. All while I'm trying to deal with his first infusion tomorrow. His one son is in denial I think, all the kids live a distance. It's a second marriage so you have the ups and down of a joined family. Our grandkids are so far away. We were supposed to go to Canada to see the one grandson icehockey. He's a goalie, but I had to cancel because of the infusion and whatever side effects tomorrow. I was afraid to fly with all going on. So for now, we're not doing Canada. My husband started Cerefolin, a brain supplment. I'll have to look at CLint Steele. the eating clean food is key, I believe in that too. I notice my husband's appetite isn't the same; that worries me. Everything worries me right now, It's just the fear of the unknown I think and feeling like we're gambling against time. THanks for your post. Quite helpful.