Honoring my hands today.
I have moved into reading, composing and posting here on blog these days. This is from a relatively focused life making things with my hands over many years. In the last 12 years before my final retirement I would wake up at night thinking about creations in clay, and how to sell them. The latter was not half as much fun, nor as therapeutic as the former.
Now I comment on blogs of my friends with whom I catch up frequently, and am among the few bloggers who reply to comments. It has to do with time available, and maybe lack of other interests to pursue.
I'm basically an echo of my former self. My word-finding ability to express myself usually happens eventually, or I can find a work-around. But my hands will continue to shake more and keep me from doing much but typing on keyboards…avoiding all hand activities which most creativity depends upon. Even mouse-movements sometimes are difficult. This is the life with Essential Tremor.
I think this leads me to take some photos of my hands and do some grief work - which I may or may not share here. But it has been interesting to go back through a few folders to capture what these hands were doing. The photos miss the actual creativity of my clay work, painting watercolors, and fiber work, like knitting or quilting. But here's what I've found. (Just in the last year.)
Just one glove for this iPhone photographer at the Christmas tree store in November 2025. I can usually capture a photo but have a lot of trouble writing texts on the phone. Thank heaven for audio dictation even with all it's glitches.
In Aug '25 I pushed myself to go see these waterfalls with friends, with my handy walking stick. (Next month I was in the hospital for second time in 6 months with pneumonia!) Having Bronchiectasis means my lungs work harder and cause almost constant coughing to clear the mucous.
July 2025, many Sunday mornings I met friends for coffee and pastries at Four Sisters Bakery, where eating outside was enjoyable. So far I can hold a cup without too much shaking, and most bites of food arrive in my mouth on my fork. Finger control seems to be the worst of my Essential Tremor so far, which is slowly deteriorating, though they work better in mornings than evenings. Drugs do not help though they did for a while! Now I have to balance breathing needs with the shaky fingers in considering drug help.
A very small silly goal was to make a snowball on the way to Telluride...where snow was still piled next to overlooks.
So I'll stop with my hands of 2025. Maybe share some more sometime down the road.
How do I feel about the loss of hand-usefulness? I'm sure not happy about it. As an artist all my life, I've had a screeching halt to my creative loves. But I can still see what I like, and for now taking photos can convey sharing beauty with others.
I finally started telling staff at a doctor's office that I have a disability in that I cannot fill out forms (which they want me so much to do!) I'm going to start asking for that to be flagged on my charts.
I have a daughter-in-law who also has hand difficulties as a result of an accident when she was in her teens. She has proved she can do just about everything as a loving wife and mother of three beautiful daughters. So her drive and positive attitude are an inspiration for me.
Coping. That's the term I think I've embraced as a senior. Coping with life's many changes. Reduced expectations definitely. But finding small things that are satisfying, and sharing gratitude.
I'm perhaps a bit foolish in some of my decisions, but am not going to skip the wonderful times I can have because of my weaker systems. It's strange to find oneself at 83 with some things that still work fine, and others that have decided to just go kerplunk!
I'm very very grateful for the muscles in my legs which now allow me to climb a flight of stairs, without having to pull myself up with the railing. That's a big accomplishment at this time, and I owe it mainly to staying with my son over Thanksgiving where I had a bed and bathroom on the second floor of their home. Plus I try to climb a flight of stairs every other day. I still get out of breath, but the handrail now is just in case I should trip.
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I did a quick search and found that exactly two years ago I had an Occupational Therapy evaluation of my hands, so here's that post, though really not that interesting.
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