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
I Was Fine a Minute Ago: My First Year with Myasthenia Gravis
Read an excerpt from this new ebook, full of humorous and honest
tales about life with myasthenia gravis.
Webinar Recap: Is It Safe to Exercise with Myasthenia Gravis?
Sarah Wright, DO MS, joined us on March 20 to discuss a hot topic in
the MG Community
The “Rocky of Rap Media” Takes on MG
Here I was in my early twenties, my work was getting known all over
the world, but I was secretly battling a potentially life-threatening
disease
2024 Rare Disease Week on Capitol Hill
Siobhain Carolan, who lives with congenital myasthenic syndrome,
discusses her experiences advocating for those with rare diseases at 2024 Rare Disease Week
on the Hill.
My CMS Journey: How the Right Diagnosis Changed My Life and Led Me to Advocacy
Siobhain shares how living with congenital myasthenic syndrome
helped her become a fierce advocate for those with rare diseases.
Making the Most of Your Doctor Appointments
Dr. Heather Finlay-Morreale, a medical doctor who lives with MG,
shares tips for preparing for your doctor’s appointment and making the most of
the time you have with your provider.
Exercising When You Have Myasthenia Gravis
Is it safe to exercise with myasthenia gravis?
Remembering Tom Larsen, the Incomparable “Rocket Man”
In February the MGFA and the MG Community lost a dedicated volunteer
and champion advocate of patients and caregivers. Friends and staff remember his
legacy.
Exercising When You Have Myasthenia Gravis
Is it safe to exercise with myasthenia gravis?
Does Madame Web Have Myasthenia Gravis?
Get to know the main character of the newest Spiderman
film