for women with Myasthenia Gravis
We are so much more than our disease. Myasthenia Gravis is something that we have. It is not who we are. I believe that we can advocate, increase awareness, fight, and remain hopeful without identifying as our disease. MG is Continue Reading
It is with a very heavy heart that I write this today. WWMG member and amazing MG warrior, Wendy Wyatt passed on yesterday. Wendy was possibly the strongest MG warrior I ever met. Wendy has been my friend for years Continue Reading
When the television show Empire wrote their lead character Lucious Lyon, played by Terrence Howard, as having Myasthenia Gravis many media articles wrote that they had “never heard of MG”. We, in the MG community, understood this. Many of us Continue Reading
Today marks two years since I gathered with approximately two dozen of my closest friends who were women with MG. Together we began the first support group specifically for women with the rare autoimmune neuromuscular disease called Myasthenia Gravis. We Continue Reading
One of the most frustrating things about having a chronic illness is that anytime you push yourself to do something that you aren’t really able to do, there is always some smart alec who says, “Oh she must not really Continue Reading