Myasthenia Gravis Foundation of America, Inc.
Samantha Masterson serves as the CEO and President of the Myasthenia Gravis Foundation of America, Inc. since February 2020. Prior experience includes positions as Vice President of Donor Stewardship and Regional Vice President for the Northeast at March of Dimes from December 2017 to January 2020, as Chief Advancement Officer at the National Brain Tumor Society from March 2015 to July 2017, and as DVP at the American Liver Foundation from December 2010 to March 2015. Samantha also held the role of Director of Development & Marketing at Alternatives Unlimited, Inc. between 2008 and 2010, and was the PR & Community Relations Manager for the A.J. Wright Division of The TJX Companies, Inc. from 2005 to 2008. Educational qualifications include a Bachelor of Science degree in Communications from Ithaca College.
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Myasthenia Gravis Foundation of America, Inc.
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 profound, debilitating 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.