Saturday, July 16, 2016

MS and the little things

Sometimes when we talk about MS we talk about big things like mobility or treatments. But it’s the little things that seem to affect me the most.

The biggest little thing that irritates me is the loss of my dexterity and fine motor skills. It started with a little curling of the fingers on my left hand. I found my resting position was a balled hand, almost a fist. Every time I noticed this, I would straighten my fingers.

Then my right hand became affected. I found it increasingly difficult to use a computer keyboard or to write. Thankfully, my employer provided me with speech-to-text software that has helped as a work-around.

As my right hand grew increasingly weaker, the realization that I could no longer sign my name was distressing. I also came to find eating difficult with heavy silverware or fatigued hands and arms.

I'm a creative person and, unfortunately, MS is robbing me of my craft hobbies. I can no longer write in a journal or do more intricate bead-work, or even do coloring, which I found soothing before the adult coloring book fad took off. I continue to work at these things when I can but the fatigue and loss of fine motor skills means I can do these activities for only brief periods.

This infuriates me - especially as I can't understand why I can't manage such a simple operation which I managed effortlessly for the first part of my life. Now buttoning a button is an almost insurmountable task.

My employer graciously lets me work from home full time. This enables me to save energy getting ready for the day without a commute that can be exhausting but I miss daily face-to-face social interactions. I have to work at being alone without being lonely. I also tire quickly and thoroughly. I’ve learned I can handle one activity a day. My illness has forced me to adjust to a simpler life.

I have adapted to life in a wheelchair. But a little thing like a curb or a step stops me in my tracks. 


“It’s the little things.”