2025 National Patient Conference
Watch sessions from the 2025 National Patient Conference, held March 31 - April 1 in Phoenix.
Author: Kate Stober
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
My MG Story: Danielle’s Journey with Seronegative Myasthenia Gravis
Danielle wants to share her treatment journey to help others understand the challenges of finding the right approach.
MGFA and Bionews Partner to Deliver Myasthenia Gravis News to Wider MG Community
Myasthenia Gravis News, delivered by Bionews, is an online news source intended to provide the myasthenia gravis (MG) community with the most recent news and information about MG, as well as first-hand community perspectives from patient and caregiver columnists.
A Mother’s Commitment
"The driving force behind my commitment to the MGFA is to help people know about MG."
How to Create a Fundraiser for the Myasthenia Gravis Foundation of America
If you’re passionate about supporting the MGFA, organizing a local fundraiser is a great way to raise awareness and generate funds for research, patient support, and advocacy.
Physical Therapy and Myasthenia Gravis – Webinar Recap
Is it safe to do physical therapy or exercise when you have myasthenia gravis?
Jesse’s Story: How Generalized Myasthenia Gravis Affected My Career
A story about changing directions and paving a different path forward
Disaster resources for individuals with MG
Steps to help you prepare for the worst
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.