Genna Mvalo is currently the National Director of Patient Registry and Industry Affairs at the Myasthenia Gravis Foundation of America, Inc., where responsibilities include overseeing cross-functional projects and managing data-driven initiatives to enhance patient registry engagement. Prior experiences encompass roles such as Junior Associate at S. Sutton & Associates Inc., Director of Development at Villages in Partnership, and National Director of Patient Advocacy and Community Engagement at the same foundation. Additional positions include National Director of Development at Patient Empowerment Network, Associate Director of Development at the National Brain Tumor Society, and Community Health Advisor with the Peace Corps, where significant achievements involved health education initiatives. Genna Mvalo holds a Bachelor's degree in Public Health and Biology from Boston University.
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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.