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My Journey Living with Myasthenia Gravis: Gloria’s MG Story
"Little by little, I learned to listen to myself, recognize my limits, and understand that asking for help is not a sign of weakness but an act of courage."
LATEST FROM THE MGFA INSIDER BLOG
Functional Fueling: Nutrition Strategies to Support Life with Myasthenia Gravis
In a recent MGFA webinar, Katherine McWaters, a registered dietitian from Nashville Nutrition Partners, shared practical, evidence-based strategies to help individuals with MG support their health through food.
Webinar Recap: Financial Assistance Resources for the Myasthenia Gravis Community
Affording care for myasthenia gravis remains a challenge for many patients. Find practical guidance on navigating patient financial support programs.
A New Era for the MG Patient Registry: Empowering Patients, Advancing Research
MGFA is proud to announce the next stage in the evolution of the MG Patient Registry: the Vitaccess Real MG Registry.
Navigating College When You Live with Myasthenia Gravis
How does MG change the college experience?
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
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.
From MG Patient to Nurse: My MG Story
I always say, “I don’t get frustrated – I get determined.”