The first time I heard the diagnosis Myasthenia Gravis it was from a local neurologist that did not believe in me or my symptoms or that I had Myasthenia Gravis!
About a month earlier I spent a week in my local hospital after loosing my ability to walk one day at work. I had been noticing other strange symptoms but never put them together. I was working full time as a teacher’s assistant to students with emotional and behavioral disorders. The job was intense, you had to think and move fast!! Students questioned me why my hands were always shaking, why was I not playing at P.E. anymore with them. Why was I walking so slow, why was my voice sounding funny? Children pick up things very quickly and as I was dismissing my notable symptoms, my students kept asking questions. I had previously had 3 back surgeries including a spinal fusion, so I contributed my leg weakness to ongoing issues with my back but it did not explain why my arms felt so fatigued or my voice getting hoarse. My symptoms progressed to the point where they could no longer be ignored, I needed answers!