Latest Post
Nicole’s MG Story: A Working Mom’s Journey with MG
Out of nowhere, blurry and double vision struck. It was myasthenia gravis.
LATEST FROM THE MGFA INSIDER BLOG
MGFA Invited to Participate in the INSPIRE Advisory Board and MSMilan Patient Community Day Conference
Collaborating with others to drive increased awareness about rare
disease around the world
Learn about Medical Financial Assistance from the PAN Foundation
Amy Niles of the PAN Foundation shares how the organization can help
MG patients pay for out-of-pocket prescription medicine costs.
Running the NYC Marathon for a World without Myasthenia Gravis
MGFA sat down with MG patient Julie and her boyfriend, Zack, who is
running the marathon for MG awareness, to talk about why supporting the MGFA matters to them
both.
My MG Story: Getting My Smile Back
As a new mom, Hannah Ensor faced challenging and confusing medical
symptoms.
Requesting Accommodations for Myasthenia Gravis at Work
Tips for ensuring you are seen, heard, and
accommodated.
Triumphant Summa Cum Laude
What it’s like to go to college while battling
myasthenia gravis
I Want to Throw a Pity Party, But No One Will Come
Greg Josephs leans into a positive life to manage myasthenia
gravis.
This Isn’t My Story, But It Is My Life: My Father Has MG
I was five years old, and I didn't understand what was
going on. All I knew was that I was scared.
A Tribute to Stan Way: A dedicated Volunteer Leader in the MG Community
Remembering a visionary educator, community builder,
and champion of the internet’s power to create connections.