My MG Story: Victoria Discusses Life and Work with Myasthenia Gravis
Nine years ago, Victoria woke up with MG symptoms. She shares her experience with diagnosis and treatment in a small town.
Author: Kate Stober
What gives you hope?
The MG Community shares what keeps them going, despite the hardships of the disease.
Highlighting Our Loved Ones During National Family Caregiver Month
Discover two powerful stories of love and perseverance.
A New Era for the MG Patient Registry: Empowering Patients, Advancing Research
MGFA is proud to announce the next stage in the evolution of the MG Patient Registry: the Vitaccess Real MG Registry.
Navigating College When You Live with Myasthenia Gravis
How does MG change the college experience?
Nicole’s MG Story: A Working Mom’s Journey with MG
Out of nowhere, blurry and double vision struck. It was myasthenia gravis.
Invisible No More
Three musicians living with myasthenia gravis come together on the song "Invisible People" for MG Awareness Month
Walking for MG Awareness in Halifax
Struggling with MG symptoms but determined to make a difference, Nadine steps out of the shadows.
2025 National Patient Conference
Watch sessions from the 2025 National Patient Conference, held March 31 - April 1 in Phoenix.
Laughing Despite (and, Sometimes, Because of!) Myasthenia Gravis: An Interview with Jane Marla Robbins
An actor and author living with MG shares how humor helps her cope