I think this is probably the key to everything you just discussed, Alice. As patients dealing with MG, as in any other disease, we are our best advocates. Simply being content with the existing treatment options and the lack of research done on MG does nothing but perpetuate and exacerbate the struggles we go through on a day-to-day basis. Not only do we, as patients, have to be our own advocates, but we need to create a greater awareness to the disease in order to further interest in the study of it.

I guess the real question, is how do you go about creating awareness? And how do you translate that awareness into further research and study of the disease?