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Why diagnose obvious MCI?

Caregivers: Dementia | Last Active: Jan 11 8:07am | Replies (17)

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@maryvc

Last week I cried with my therapist. I was feeling sad because I miss Steve. The Steve who was an active partner, decision maker, and confidente. It is hard. I probably say too much, correct too much and then control too much, yet I still can’t just treat him as if he can’t help it yet for the most part he can’t help it. I guess the emphasis should be on celebrating the good times and celebrating when I am doing good with all this.
I get your energy. We have a lot in us. But I remember what my friend whose husband had Parkinson’s told me. You have to slow down now; be patient and appreciate every moment.

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Replies to "Last week I cried with my therapist. I was feeling sad because I miss Steve. The..."

My husband was diagnosed with MCI last year. I feel the same way you do about missing my friend, husband, and partner who used to be there. It IS hard to accept that he's gone while simultaneously remembering that this is still him...that he's still in there sometimes, somewhere. That requires some nearly impossible mental gymnastics. My new goal is to try to focus on hope. I know he won't get better, but I hope I can make myself strong enough to appreciate the time we have left. It's so easy to get depressed about it.