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
My MG Story: Diagnosed as a Teen, Emily’s MG is in Remission Thanks to Thymectomy
Boyle Family Realizes the Powerful Benefits of
Thymectomy.
New Book by a Leading Doctor Will Help You Cope with Myasthenia
All proceeds from Coping with Myasthania
Gravis book will benefit MGFA
Newly diagnosed? Here’s What You Need to Know.
Newly-Diagnosed with MG? Here are Some First Steps to
Take
Evan Greene Reaches New Peaks in Spite of His MG
Evan Greene’s Climbs Mount Whitney – MG
Cannot Take His Spirit and Sense of Life
From MG to MD: a story of hope and persistence
MG patient is inspired by his disease to enter healthcare and become
an MD.
MG Patient Advocates Make Their Voices Heard During Rare Disease Week 2021
MG Advocates Describe Their Experiences During Rare Disease
Week
We’re Not Alone: Creating a Spanish-Language Support Group
Leah Gaitan-Diaz conducts Spanish speaking support groups to close
the language gap for the MG Community.
Rituximab: Why B cell reduction therapy doesn’t work for all MG patients
Kevin O’Connor, PhD discusses why some MuSK MG
patients relapse after Rituximab.
Helping People Understand and Experience Myasthenia
MG patient Rebecca Molitoris demonstrates to others what it feels
like to have MG.
