The Myasthenia Gravis Rare Disease Network (MGNet)
Patient Advocacy Groups (PAGs)
The Myasthenia Gravis Foundation of America (MGFA) is a national, non-profit organization that serves the Myasthenia Gravis patient community. MGFA’s mission is to enhance lives, create connections and cure MG through programs of patient services, public information, medical research, professional education, advocacy and patient care.
Conquer MG or Conquer Myasthenia Gravis is a non-profit organization with mission to facilitate the timely diagnosis and optimal care of individuals affected by myasthenia gravis and to improve their lives through programs of patient services, public awareness, medical research, education, advocacy and patient care.
This website is hosted by the networks’ Data Management and Coordinating Center at Cincinnati Children’s Hospital Medical Center, which is funded by NCATS and the National Institute of Neurological Disorders and Stroke (NINDS) under grant number TR002818.