MGFA Vision
A world without myasthenia gravis
MGFA is committed to finding a cure for MG, improving treatment options, and providing information and support to people with myasthenia gravis through research, education, advocacy, and community support programs.
Jasmine Snow shares her journey with MG and how she decided to get involved. Read her story here.
Zach Knowles and Whitney Miller share the stories of their fathers' MG diagnosis. Read the complete story here.
Edwin L. Kennedy shares the story of his son's MG diagnosis. Read the complete story here.
Julie Buckholt shares her story of life with MG. Read the complete story here.
Annette Kennedy-Bowman shares the story of her life with MG Read her complete story here.
Your donation will enable MGFA to continue their vital work supporting research, developing diagnostic techniques and treatments, and providing professional education and family outreach programs.
Living Healthy and Active Lives: The Patient Perspective
Myasthenia Gravis and Pregrnancy
A discussion about therapies for MG
Top 5 lists of what a patient needs to know about living with MG
Prescription drugs and MG
Overview of MG: Part I
Overview of MG: Part II
Influenza vaccine for patients with MG