Dealing with a Spouse with a “Mild Cognitive Impairment”
My husband was diagnosed with MCI in 2019. He is pretty independent, just forgetful of time, dates, location of places, anything electronic & events from our life together (we’ve been married 52 years). It’s all just getting to me. I find myself wanting to be alone so I’m not continuously reminded of these changes. Because my friends/family are out of state, working, or involved with their own families, I really have no one to talk to so I’m seeing a therapist twice a week to deal with the sadness, anger, grief I have over his condition. I just wonder if other women find themselves in this position & how they are dealing with it.
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@gilkesl I think airplane stewardesses have the best advice. When they tell you ehat tondo when the face masks cone down, the say to put YOUR OWN mask on FIRST, brcause if YOU pass out, there's no one to help the others. So care takers need to take care of themselves, because otherwise their Carees have no one to take carr of them.
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9 Reactions@upgirl2013
This is a horrible disease. I am currently shut away in our closet trying not to hear his phone conversation with a friend.
We were in a car accident recently and he is calling all his friends to tell them about it, but he has to start with why we were in the car- where we were going, why, etc. It takes a few minutes to get to the point.
After the wreck I was very shaken and upset. I asked him for a hug- which we rarely do anymore - and he said he did not feel like hugging anybody.
It is so sad and I feel so lonely. Bereft is a good word. My friends help with texts of support but they cannot give me what i really yearn for and need. My husband’s arms around me.
I am trying to stay busy so I cannot think- just buckle up and keep moving- and praying. Jesus is going to hear from me a lot today.
To my friends in this group and in the same boat- I wish you a blessed new year. May 2026 be brighter for you - in whatever way possible.
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10 ReactionsDo tastes change? My husband has always loved salt, and salts his food before even tasting it. All of a sudden, he is starting to complain that foods are too salty.
@minniem I am so sorry that you have that horrible lonely feeling. I hate those moments. “It’s by hard the hardest thing I have ever felt: To be so in love with you, yet so alone” Mary Travers
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4 Reactions@blc1951 - I believe they do. Or maybe the brain is not receiving the same signals from the taste buds. For my spouse - it is hamburgers and casseroles - and unfortunately- fish sticks.
Of course, I still love Little Debbie Christmas Trees, so I have my nostalgia foods, too.
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3 Reactions@minniem
Hello, and first off so very sorry about your accident. I hope you are not injured or sore.
I am responding because of your hugging comment. My husband's brother died in July, no tears from him and hardly a reaction. I asked him if he wanted a hug after we found out, and he said no. I guess I needed a hug after losing my Bro in law, but there is no hugging or touching anymore and I too long for his comforting arms around me. That lack of intimacy is one of the worst parts of dementia.
Happy New Year anyway.
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2 Reactions@blc1951
Yes, I just took a dementia class and they mentioned that the senses are affected. One of the last senses to remain intact is the taste of sugar. My husband has developed quite the sweet tooth since his diagnosis, and he wasn't that into sweets before. Now I have to limit or hide the sweets in the house.
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4 Reactions@upgirl2013
Such a lovely John Denver song. 😊
@blc1951 Your post made me realize that when my husband one day said he would not eat green beans, it’s probably because of his dementia. He’s in great good humor as always, but oddities are popping up more frequently. Apparently tastes do change. Thanks for posting.
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2 Reactions@judimahoney my husband’s request for nightly dessert makes sense now.
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