Short bursts of energy

There’s a support group that «puts the I in caregiver« which I value for its honesty. It’s akin to the one urging us «to be selfish.« I take about 5 hours for myself each day. It’s a necessary indulgence. Let me try to explain what my time away does to benefit me. When I getContinue reading “Short bursts of energy”

We traveled a little

Burt had many anxieties when we first met, had had them for years. He feared train tunnels and getting stuck in them. He always faced his phobias. He planned trips for us, often by train. In fact, trains became our favorite mode of transportation. Our trips were special. We went to Mystic and spent aContinue reading “We traveled a little”

Moment to moment

Burt’s fever broke overnight, almost as suddenly as it started. He was immediately a bit less disoriented. He was able to speak more clearly. We were just chatting, and he mentioned his ex-wife‘s name. I was prepared for this. I was prepared for it to hurt when I asked who she was. He did say,Continue reading “Moment to moment”

Grateful, appreciative, and thankful

It’s Thanksgiving. Talk of gratitude is as prevalent as the turkey on our plates. We are parsing what is worthy of our appreciation as we sit down for today’s feast. The original idea of this holiday was to show thanks to God for the bounty in our lives. Gratitude practice is at the least aContinue reading “Grateful, appreciative, and thankful”

Getting out together

I hate to admit it. When apparently healthy couples of a certain age stroll by hand in hand, I am envious.  The recent outings facilitated by our new weekend aide take some of the sting of my jealousy away. I can get out with my guy. That’s a nice feeling. We both enjoy being out,Continue reading “Getting out together”

There’s a lot to be said

From pretty much day one of Burt’s symptoms, I looked to getting help. Initially, it was because I needed my time. I wanted to get 3 or 4 hours several times a week to get out. It seemed an existential need for me. In the parlance of our dementia communities, it’s deemed “self-care.” Some ofContinue reading “There’s a lot to be said”

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