Latest Post
Our MG Story: A Mission of Hope
A family's MG crisis inspires hope for others in Puerto Rico living with myasthenia gravis.
LATEST FROM THE MGFA INSIDER BLOG
How One Racing Fan Is Putting MG in the Spotlight
As Gary adjusted to life with MG, he began looking for ways to combine his professional background in marketing with another lifelong passion: racing.
Miles for MG
Strange symptoms led to a myasthenia gravis diagnosis. Now Phillip is dedicating his upcoming marathon run to his wife - the strongest woman he knows.
How to create your own MGFA community fundraiser
Advice from MGFA Ambassador Siobhain Carolan
The Strength Within: My Journey Through Pregnancy and Myasthenia Gravis
Two years ago, I shared my story to raise awareness. Today I am sharing a chapter that changed me forever.
My MG Story: Sethunya Maikano
I want people to know that those living with MG are not defined by the condition.
From Diagnosis to Remission: My MG Story
I woke up on my birthday – it was January 1993 – and I was seeing double.
Thao’s MG Story: Why I Walk for a World Without MG
Thao was healthy until May 2024, when she developed sudden-onset right-side ptosis. Supporting the MGFA's mission has helped her transform something incredibly challenging into something meaningful.
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.