Myasthenia Gravis Foundation of America

What Myasthenia Gravis Foundation of America makes

Topics myasthenia-gravis, autoimmune-disease, neuromuscular-disorder, patient-advocacy, healthcare, research, support, education

Myasthenia Gravis Foundation of America (MGFA) is the largest, leading patient advocacy organization solely dedicated to finding a cure for the rare neuromuscular disease myasthenia gravis (MG) while improving the lives of people living with MG. More than 70,000 are diagnosed and living with MG in the United States alone. Those with myasthenia suffer with profound, debilitating physical symptoms such as extreme fatigue and muscle weakness that impact a person’s ability to see, swallow, smile, walk, or breathe. MGFA is focused on funding the most promising research discoveries for better treatments and a cure while providing impactful programs, guidance, and education to help support members of the MG Community.

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