Myasthenia Gravis Foundation

Information, Education and Support: MGFA provides material, information and referral, and education and support programs to help people manage the challenges of living with myasthenia gravis. MGFA is a national organization that supports the delivery of programs and services through a myriad of channels including a network of approximately 28 support groups, Partners in MG Care and a number of other networks nationwide. The MGFA website is one of the organization's greatest resources and is a premier source of information. MGFA also hosts a number of live and interactive educational forums, including 18 wellness and research webinars as well as hosted eleven Community Health Fairs in various US cities for MG patients and caregivers to interact, obtain information and learn about MG research and treatment developments from MG experts and corporate industry leaders. MGFA annually hosts a National Patient Conference, a gathering of the MG Community which features MG research updates, patient stories, news about MG treatments and discoveries and many exciting educational topics to help patients and caregivers manage their MG journey. MGFA has also developed an Online Community platform which is a one-of-a-kind virtual neighborhood where the MG Community can connect, share ideas and discoveries and access MG-specific educational materials such as live broadcasts, webinars and information libraries in one place. MGFA also maintains an extensive website which provides patients and caregivers with educational content and news as well as Facebook page to promote awareness and the Organization's educational mission.