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bill2001 avatar

The Caregiver’s Brain

Caregivers: Dementia | Last Active: Aug 17 8:47pm | Replies (32)

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Profile picture for 4goakley    Kathy @4goakley

I can SO relate ! Thank you to bill2001 for the wonderful description of "brain reset".
Like many other respondents, I am still dealing with my spouse's early stage dementia. It is sad to give up our previous life of meaningful conversations, active travel, rewarding community work and social interactions.
I am trying to reset my brain. I will organize a scenic local bus tour instead of a trip to Europe, or a lunch out with friends instead of a night at the theatre.
Simple things. A shopping errand becomes the day's activity. My motto is "do what we can while we can " and I remain grateful for all that we COULD do in the past. Blessings to all !

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Replies to "I can SO relate ! Thank you to bill2001 for the wonderful description of "brain reset"...."

I read over my last comment and realize how self-centered it sounds, but I needed to get some things off my chest. That doesn't mean I'm totally miserable or pity myself for what my husband is going through. I'm a homebody by nature, so I'm more content than some would be to just hunker down. I need to work on making myself get out more. I, too, find a trip to the grocery store enough excitement for one day or a couple of hours spent with a good friend. There are so many in much, much worse situations than mine, and I'm grateful for the life I've had and still have. My husband is a good, kind man, even if he can't remember my birthday or his grandson's name. But despite the gratitude there are times when negativity takes over and has to go somewhere--like to this forum. A friend once said, Patience is a virtue. The only virtue.