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]
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About Advocacy Partners
The information above is provided by our partner. Learn more about our advocacy partners here.
Recent Posts
- The long journey to diagnosing my seronegative myasthenia gravis
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- 1st patient enrolled in Phase 3 trial of MG cell therapy Descartes-08
- Battling 2 enemies: MG and the broken US healthcare system
- After years of flare-ups, I achieved myasthenia gravis remission