Latest Post
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
LATEST FROM THE MGFA INSIDER BLOG
Our MG Story: Advice for Spouses and Caregivers
In this vlog, Cary asks her husband Zack some questions about his
experience as an MG caregiver.
Our MG Story: When Your Child Has Myasthenia Gravis
The Oronuga family’s life was turned upside down when
Teniola was diagnosed with MG at age three. They share what it is like to battle this
chronic autoimmune condition in Nigeria.
Our MG Story: The Stehlik Sisters Give Back in Memory of Their Pops
An MG diagnosis leads to a passion for raising awareness and giving
back.
Her Fight is My Fight
Raising awareness and racing for a cure with a one-of-a-kind
fundraiser.
Spotlight on the MG Community: Paul Strumph
Learn more about a key member of our volunteer Board of
Directors.
Why the MG Walk Matters to Me
It's more important than ever to restart the MG Walk.
We’re closer than ever to a world without MG. But to get there, we need
you.
Running the Denver Colfax Marathon for a World Without Myasthenia Gravis
“We want to find a way to give back to an organization
that’s been tremendously helpful to
us.”