MG Patient Advocates Make Their Voices Heard During Rare Disease Week 2021
MG Advocates Describe Their Experiences During Rare Disease
Week
Author: Genna Mvalo
MGFA Partners with Rare Across America to Advocate for MG Patients
Volunteers Ensure Political Leaders Understand the Challenges of
Rare Diseases like Myasthenia.
MGFA Pilot Grant Awards Announced for 2020
MGFA is pleased to award research grants each year to help advance
the understanding of myasthenia gravis. Congratulations to the amazingly creative medical
professionals and researchers who earned the 2020 funding grants.
MGFA PILOT GRANT AWARDS ANNOUNCED FOR 2020
The Myasthenia Gravis Foundation of America (MGFA) is pleased to award research grants each year to help advance the understanding of myasthenia gravis and ultimately find better treatments for the disease. We fund some of the most promising and results-oriented MG research around the world to help improve the lives of those living with myasthenia […]