June is Myasthenia Gravis Awareness Month. Every June for the past five years, I’ve thought about writing something but always come up short, because what is worth saying?
Should I share my diagnosis story? Should I try to detail all the ways myasthenia gravis has shifted the direction of my life?
Should I list the symptoms so people might be better able to recognize it in themselves or others? Having myasthenia gravis means sometimes I use a cane… My diagnosis was swift and too long ago to matter.
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