I have only been
physically disabled a few times in my life, and the memories of each occasion
still haunt me. The first time I had that experience was when I was pregnant.
With each of my daughters, I was so sick during pregnancy that I was often
called “an invalid,” usually by my husband. Both of our offspring stayed in the
womb so long they were overdue. I didn’t glow, I didn’t have wonderful food cravings
– I just wanted it to end! And each time, had unbearably long labors, followed
by C-sections. My eldest daughter just had a similar pregnancy experience, and
I “felt her pain” every time we spoke. I am proud, though, that she was a
better patient than I was! Having surgery, complete with staples-two-ways, for
the delivery of each daughter put me in a whole new realm of disability!
Although I was young then, the details of the C-section delivery left me in
lots of agony. But, both times, I foolishly couldn’t wait to leave the
hospital! I couldn’t stand the idea of having someone take care of me!
The next time I
suffered an injury was a minor one – but it was very inconvenient for an
organist to have a broken wrist, especially since it happened when my second
daughter was very young. Having a cast on my left arm, not being able to take a
bath or wash my hair by myself, left me very frustrated! I had to find music
for the right hand only to play for church. Once again, I couldn’t wait to get
that cast off!
About ten years ago, just
after learning that I had HD, I suffered an injury while working at Esperanza.
I fell off the stage, and broke my left knee and my right ankle. Not wanting to
worry the clients there (by calling an ambulance), I tried to walk to a waiting mini-bus for a ride to
the immediate care center. That was one painful journey! When I learned the
extent of my injuries, I had to leave work for a minimum of two weeks, so that
a claim could be made for Workers Compensation. Once again, I was the worst patient in the world, trying
to keep working even though I was broken! At home, my husband borrowed a
wheelchair for me to make trips up and down the hall. It was that same
wheelchair that we brought to our oldest daughter’s college graduation. We all
vividly remember being ushered to the handicapped section of Krannert Center at
U of I – with my elderly mother-in-law pushing
me! We did have the best seat in the house.
Being unable to walk
really wreaked havoc with my exercise plans! During this time of being an
invalid, I found an exercise VHS called Chair
Dancing. Buying things online was a little more difficult ten years ago,
but I was so delighted to find that tape! Some of it was too difficult for me
at first, but as my bones healed, I tried to keep my muscles limber by doing parts
of the exercises each day.
I dread the day when I truly become an invalid, knowing that I am truly the worst patient in the world. What will it mean for my loved ones? Will they have difficult decisions to make? How will I respond to them?
The reason I illustrated this blog with a picture of a Chair Dancing video is that I still use those videos, and many of the newer versions (Chair Dancing Through the Decades, Life's a Celebration, Sit Down and Tone Up, and many more)! The Alzheimer's patients that I work with each week love doing chair dancing! I've gotten some great movements from those videos, and often make my own list of songs for each new "Circle Dance." Hopefully, if and when I am confined to a wheelchair again, I'll be in the mood to chair dance!
The reason I illustrated this blog with a picture of a Chair Dancing video is that I still use those videos, and many of the newer versions (Chair Dancing Through the Decades, Life's a Celebration, Sit Down and Tone Up, and many more)! The Alzheimer's patients that I work with each week love doing chair dancing! I've gotten some great movements from those videos, and often make my own list of songs for each new "Circle Dance." Hopefully, if and when I am confined to a wheelchair again, I'll be in the mood to chair dance!
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