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Why diagnose obvious MCI?

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

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@maryvc

We avoided an evaluation, thinking it’s all “normal aging” until we could not deny that things were more and more off-anxiety w driving, leaving a meeting w our financial advisor or CPA and my husband not able to recall what was discussed- I took notes. Also spacial recognition - inability to help hang a mirror- my 92 year old neighbor helped hang it in a few minutes. I made appts for a Neuropsych eval but his PCP wanted him to see a geriatrician, sleep specialist and have cardiology exams. The latest MRI did show micro vascular changes.
So we went to the geriatrician. After 3 hours of interviews and testing w the social worker, the Dr. confirmed Mild Cognitive Impairment- not dementia yet- and since has ordered a speech therapist twice a week for cognitive development. My husband also had to have an extensive drivers test w an occupational therapist.
We also worked with two neuropsychologists.
It was a difficult year. Denial, anger, confusion and finally acceptance and moving forward. Traveling as much as time allows with time left to enjoy each other.
I have taken over all the finances and home management and planning.
Also all of these evaluations were covered by Medicare and our supplementary insurance because we have a documented diagnosis and plan.
Very important is to determine who you are seeing for the eval and who you will be following up with. Our doc was realistic but gentle and helpful.

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Replies to "We avoided an evaluation, thinking it’s all “normal aging” until we could not deny that things..."

I appreciate hearing about your journey and wish you well. Sometimes I catch myself thinking I am imagining the changes or at least, exaggerating them. Family and friends don't say anything. Do they no notice? Are they trying to be polite? I dread the conflict I anticipate in trying to get her to go to be evaluated. Sharon

Thank you for sharing the details of your story. So much of it is like our story. The MCI diagnosis has motivated my husband to improve his exercise, change his eating, pay more attention to sleep and realize the social life is important too. It is amazing to me that he’s done this, despite the fact that he really doesn’t believe the MCI diagnosis. Maybe that doesn’t matter as long as he acts on it.

These past three months have been completely revamping our lives, so that I could take over the important finances and so much more. It is the first of January 2024 and I realize I need a support group so I can have someone to talk to about all this.