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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@slarson14
It's possible there is something going on. If my husband is engrossed in something (usually word search puzzles or on his phone), nothing else exists. He doesn't hear me when I talk to him, notice I am in the room, no awareness of anything else except what he's focused on.
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1 Reaction@annie1946 Me too !
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1 Reaction@tuckerliko Likewise. The changes. . . I never dreamed this would happen. Lonely as he is “gone” a lot. It’s often like I am just one person here.
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1 Reaction@kjc48 KC. Thanks for your input, after much research and anguish, we have decided against going forward with the infusion treatments…we will never know if this is the right or wrong decision (if there is in these situations) but we are comfortable with this and after 53 years together we will make this work and enjoy the good times
Thanks to all
Joe
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5 ReactionsAny decision is a good decision and being positivite regardless of what we decide is a good thing.
Enjoy your 53 years together, one day at a time. That's all we can do. Best, Karla
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3 Reactions@dederickve
It messes with my mind that I am terribly lonely with my husband by my side. Luckily we have a dog that I speak to all the time. If I speak to my husband and he doesn't answer, I turn to our dog for conversation and much-needed pets.
Some folks on this forum talk about seeking others to be with for physical touch, etc. I just can't imagine doing that while still married, but I totally understand the temptation for deeper connection.
Hugs all around folks. 🫂
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5 ReactionsHas anyone taken special videos or audio recordings of their MCI spouse to listen and/or share with family later? People often do this with end stage ALS or cancer. Heading into the depths of MCI your loved one’s voice, like @judimahoney mentioned, may be lost.
I’m more fond of audio recordings - maybe of a story they often tell or a favorite subject. A recording of a time well spent with a child or grandchild would be lovely to share in the future years.
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2 Reactions@2me
Thanks
@slarson14 Definitely sounds like some form of cognitive impairment.
@judimahoney , for me it helps to hug friends and family. Accept any friendly touch offered by others. I know, it’s not the same as the touch from your special person, but it helps. Receiving no physical touch for weeks is devastating to the soul.
Hug your dog.
🌻
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6 Reactions