Latest Post Nicole’s MG Story: A Working Mom’s Journey with MG Kate Stober | June 19, 2025 Out of nowhere, blurry and double vision struck. It was myasthenia gravis. Read More
Community Fundraising Her Fight is My Fight Kate Stober | May 30, 2024 Raising awareness and racing for a cure with a one-of-a-kind fundraiser. Read More
Living with MG Stories Life After Corticosteroids Krystel El Koussa | May 15, 2024 This is not a weight loss journey. Read More
MGFA News Spotlight on the MG Community: Paul Strumph Kate Stober | April 22, 2024 Learn more about a key member of our volunteer Board of Directors. Read More
Community Fundraising Why the MG Walk Matters to Me Kate Stober | April 18, 2024 It's more important than ever to restart the MG Walk. We’re closer than ever to a world without MG. But to get there, we need you. Read More
MG Articles Running the Denver Colfax Marathon for a World Without Myasthenia Gravis Kate Stober | April 10, 2024 “We want to find a way to give back to an organization that’s been tremendously helpful to us.” Read More
MG Articles I Was Fine a Minute Ago: My First Year with Myasthenia Gravis Kate Stober | April 3, 2024 Read an excerpt from this new ebook, full of humorous and honest tales about life with myasthenia gravis. Read More
MG Articles Webinar Recap: Is It Safe to Exercise with Myasthenia Gravis? Kate Stober | March 28, 2024 Sarah Wright, DO MS, joined us on March 20 to discuss a hot topic in the MG Community Read More
Living with MG Stories The “Rocky of Rap Media” Takes on MG Scott Bejda | March 21, 2024 Here I was in my early twenties, my work was getting known all over the world, but I was secretly battling a potentially life-threatening disease Read More
Our MG Voice Advocacy 2024 Rare Disease Week on Capitol Hill Siobhain Carolan | March 15, 2024 Siobhain Carolan, who lives with congenital myasthenic syndrome, discusses her experiences advocating for those with rare diseases at 2024 Rare Disease Week on the Hill. Read More