Latest Post
My MG Story: Victoria Discusses Life and Work with Myasthenia Gravis
Nine years ago, Victoria woke up with MG symptoms. She shares her experience with diagnosis and treatment in a small town.
LATEST FROM THE MGFA INSIDER BLOG
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.
Real Talk About MG
How to explain the rare neuromuscular disease myasthenia gravis
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
A Danish Musician’s Battle with Myasthenia Gravis
A Danish Musician’s Battle with Myasthenia Gravis.
Back to Doing What I Love: My Myasthenia Gravis Story
How a clinical trial brought back my smile
How MG can affect your sleep and what to do about it
Sleep and Myasthenia Gravis: Webinar Recap
Preparing for a Medical Emergency When You Have Myasthenia Gravis
Find tools and advice to help you prepare for the worst.