Myasthenia Gravis Foundation of America
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.
Молодые исследователи делятся своими работами по миастении гравис
Вебинар: Передовая РНК-клеточная терапия аутоиммунных заболеваний
Webinar - CAR-T Cell Therapy for Generalized Myasthenia Gravis: Introduction to anito-cel
Webinar: Supporting the MG Community - Financial Assistance Programs
Webinar - Add-On Muscle-Targeted Therapy for Generalized Myasthenia Gravis: Introduction to NMD670
Walk for a World Without Myasthenia Gravis!
Webinar - Efficacy and Safety of Efgartigimod PH20 SC in Adults With Ocular Myasthenia Gravis
Webinar: The Changing MG Conversation
Webinar: Navigating Your Path - Living and working with chronic autoimmune disease
MGFA Webinar: How to Raise Awareness About Myasthenia Gravis this June – or Any Time!
Webinar: Functional Fueling - Supportive Nutrition for Myasthenia Gravis
Webinar: What a Patient Needs to Succeed
David Jack: Together WE RISE! A message for the MG Community
MGFA 2025 National Patient Conference - April 1 Sessions
MGFA 2025 National Patient Conference - March 31 - Afternoon sessions
MGFA 2025 National Patient Conference - March 31 - Morning Sessions
Treatment Advances in Juvenile Myasthenia Gravis - MGFA Wellness Webinar
Important Changes you need to know about Medicare in 2025 with @PANFoundation
Webinar: The Importance of Caregiver Self-Recognition
How myasthenia gravis impacts the whole family
2024 MGFA Scientific Session | AANEM Annual Meeting
Physical Therapy and Myasthenia Gravis: MGFA Wellness Webinar Series
Research Webinar Series: Living Better with MG: How AI Enhances Treatment and Management
Reprogramming the Immune System to Halt Myasthenia Gravis: MGFA Research Webinar Series
Research Webinar Series: UCB Generalized Myasthenia Gravis
Meet the MGFA Ambassadors - Volunteers for the Myasthenia Gravis Community
MGFA Wellness Webinar Series: Sleep and MG
Research Webinar Series: argenx Clinical Trial Update – Adapt Seron
Our Myasthenia Gravis Story: Advice for Spouses and Caregivers