Advocacy partner: Myasthenia Gravis Foundation of America

About the Myasthenia Gravis Foundation of America

Myasthenia Gravis Foundation of America (MGFA) is the largest, leading patient advocacy organization solely dedicated to finding better treatments and a cure for the rare neuromuscular disease myasthenia gravis (MG) while improving the lives of people living with MG. More than 90,000+ are diagnosed and living with MG in the United States alone. MGFA is focused on funding the most promising research discoveries for better treatments while providing impactful programs, guidance, and education resources to help support members of the MG Community and improve their quality of life.

Contact: Michael Antonellis – Vice President, Global Marketing & Communications
Phone: 617-610-2411
Email: [email protected]