MITCH STURGEON
Author and Blogger Living With MS
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I had begun to walk like a drunk, and not just on Saturday nights. Within three years of being diagnosed with primary progressive MS, I needed some ambulatory assistance. Without consulting a medical professional, I purchased a wooden cane — something that looked rugged, masculine, outdoorsy, and decidedly nonmedical. Still, I dreaded the thought of using it in public…
To read the rest of my recent article, published at multiplesclerosis.net, click here.
6 Replies to “Mobility Aids — Friend or Foe?”
Been there, done that!! Well said Mitch. Words of wisdom for those struggling and a good reminder for those that are already there.
Kathy, nice to hear from an old pro 🙂
I remember telling my employer of my MS diagnosis so they wouldn’t think I was drunk at work. I went from wall-walking to a cane (made by me out of a hornbeam sapling- very manly!) to a wheelchair that I only used at the office. Like for you, it was a gradual process, but it was pretty quick and direct. I’m now “retired,” and full-time in a power chair. I appreciate your sentiment that far from being “bound” to my chair it is a vehicle of liberation.
Stephen, nice to hear from you! Can you imagine what life must’ve been like for people with diseases like ours before power wheelchairs? In that sense, we are very lucky people.
I have a whole collection of canes including some used by my mother. I always use a cane when I go to an art gallery. I started this after I almost stumbled into some $5,000 sculptures. I also avoid shopping at places that don’t have shopping carts.
Brian, I’m so glad you’re doing what you need to do to stay active and mobile in the community.
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