Scott McCormack: Responding to fearful questions about my myasthenia gravis
Scott McCormack, who lives in California, was diagnosed in 2016. He shares the anxious reactions he gets when he reveals his myasthenia gravis diagnosis, and how he responds.
Transcript
When somebody asks what’s wrong and I tell them, “myasthenia gravis,” the overwhelming response is, “What?”
They’ve never heard of it before. And neither had I before I contracted it.
I would say the strangest or most interesting response was a few people wanted to know if it was contagious. As they were asking that, they took a step backward. But then I assured them that, “No, it’s not contagious. It’s just something my body’s doing to me. It won’t do it to anybody else.”
Recent Posts
- In moments of uncertainty with MG, who or what do we trust?
- What happens when speaking up becomes a survival skill
- I want to connect with the person who exists beyond my illness and fear
- Finding humor in the absurdity of MG helps me manage stress
- Learning how to manage fear in life with myasthenia gravis