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]
Resources
PATIENT PACKET
Request a complimentary packet full of resources to help you and your care partner navigate an MG diagnosis.
FIND MEDICAL EXPERTS
Our MGFA Partners in MG Care network includes care providers who specialize in treating people with myasthenia gravis.
MGFA HELPLINE
Whether you are newly diagnosed with MG or have been living with the disease for some time, you’re likely to have questions about MG management from time to time. Call the MGFA Helpline, and professional counselors can answer your questions about living with myasthenia gravis, provide emotional health support, and guide you to resources to help you manage MG.
MG LEXICON
Diplopia, immunoglobulin, ophthalmologist, seronegative, plasmapheresis… understanding the alphabet soup of MG can be tough. The MG Lexicon can help! Produced in collaboration with patients, medical professionals, and industry partners, our lexicon bridges the gap in terminology between doctors and those affected by MG.
Upcoming events
About Advocacy Partners
The information above is provided by our partner. Learn more about our advocacy partners here.