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DiscussionDealing with a Spouse with a “Mild Cognitive Impairment”
Caregivers: Dementia | Last Active: May 20 11:39pm | Replies (160)Comment receiving replies
Replies to "Please feel free to use this as a "woe is me" site if you need to..."
I also understand having not many relatives nearby. We have one son who lives on the west coast & I have a brother in the southwest west. He has a brother here but I don’t think he is aware of the extent of the impairment. He also has a cousin who lost her mom (his aunt) to AD so she is aware of the struggles & I keep in touch with her.
I am in a similar situation with my 80-year-old husband and have been told by our doctor that it's only going to get worse; that his heart would outlast his brain. I was prepared to do the caregiver thing but last September I had an unusually odd major stroke (basilar artery occlusion) that I survived mostly intact except I do find myself quite tired all the time and with an unstable gait. I can still cook, do dishes and some light housekeeping but now he has decided that he is MY Caregiver; afraid I might die anytime. (My doctor thinks I have several good years ahead of me.) I don't quite know how to handle this situation now. He spends money like a drunken sailor and that worries me as well. What are my options when he gets so bad I can't deal with him anymore?
Thank you for the suggestions. I’m thinking of working with a trainer to try to regain some of my muscle strength. I’ve also considered restarting music lessons. I bought a bass guitar to take up when I retired but my lessons have been off & on due to injuries I’ve sustained. I’ve also thought of taking up flute & piano which I played as a girl but have lost much ground over the years. I’m just not sure I have the stamina to do all three which sounds silly to say. I used to do 2 of the 3 with no problem at all. The stress of the MCI diagnosis has just taken so much out of me. Drained me really. I guess I will see what I am able to do (commit to).