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Snowflakes: My MG Story
I was 29 when I learned of Onassis’ death and first heard the words “myasthenia gravis.” Little did I suspect that 45 years later, those words would become a large part of my vocabulary…
LATEST FROM THE MGFA INSIDER BLOG
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.
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.
Singing in a Different Key
A passionate singer nearly loses her voice to myasthenia gravis
From Life Support to Marathon Runner: This Is Why I Run
I’m training for the 2025 TCS New York City Marathon. I’m running for everyone still fighting this disease.
Navigating College When You Live with Myasthenia Gravis
How does MG change the college experience?
Volunteer Spotlight: Trouble Nkhowani
Meet Trouble Nkhowani, who lives in Lusaka, Zambia, and proudly holds the title of our first MG Friend across the ocean. Trouble works tirelessly to ensure the MG community in his country receives the support they need. This is no small feat for a man balancing his own MG diagnosis, a full-time job, and his […]
Nicole’s MG Story: A Working Mom’s Journey with MG
Out of nowhere, blurry and double vision struck. It was myasthenia gravis.