MD and Me

Q. What is your handicap?
A. I have Muscular Dystrophy (MD). It affects the muscles by making them progressively weaker. This means that I have minimal use of my arms and legs and I use a power wheelchair to get around.
In addition, I have a tracheostomy and use a ventilator to breathe, as the lungs are controlled by the diaphragm, another muscle. These machines basically keep me alive; one minute without the ventilator and I faint. My trache tube needs to be replaced with a new one every two weeks, since it’s made of plastic and gets crusty, increasing the risk of infection. I also have a feeding tube because the muscles that I need to swallow are very weak. I can eat a little, but not enough to get proper nutrition.
As you can imagine, I always have to be with someone who can take care of me.
The doctors first thought I had Mitochondrial Myopathy, but discarded that after more tests. I may have a new type of MD and I’m thinking of naming it. Hearing, “Mr. Smith, I’m afraid you’ve contracted a condition called Superwalking,” just before hearing, “which means you’ll soon be learning to walk without the assistance of legs,” would in some way soften the blow. I’m considerate like that.

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3 Comments on “MD and Me”

  1. Brian Says:

    Hotwheels rules!

  2. Robonwheelz Says:

    Hi, do have DMD? If you do, I am one of your crippled brothers. I am thirty and have many stories to tell.


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