Kathalina Nguyen Aug 08, 2024 Living with MG Stories Back to Doing What I Love: My Myasthenia Gravis Story How a clinical trial brought back my smile Read More
Kate Stober Jun 03, 2024 Community Fundraising 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. Read More
Kate Stober May 30, 2024 Community Fundraising Her Fight is My Fight Raising awareness and racing for a cure with a one-of-a-kind fundraiser. Read More
Krystel El Koussa May 15, 2024 Living with MG Stories Life After Corticosteroids My MG story This is not a weight loss journey. Read More
Kate Stober Apr 22, 2024 MGFA News Spotlight on the MG Community: Paul Strumph Learn more about a key member of our volunteer Board of Directors. Read More
Kate Stober Apr 18, 2024 Community Fundraising Why the MG Walk Matters to Me 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
Kate Stober Apr 10, 2024 MG Articles Running the Denver Colfax Marathon for a World Without Myasthenia Gravis “We want to find a way to give back to an organization that’s been tremendously helpful to us.” Read More
Kate Stober Apr 03, 2024 MG Articles I Was Fine a Minute Ago: My First Year with Myasthenia Gravis Read an excerpt from this new ebook, full of humorous and honest tales about life with myasthenia gravis. Read More
Kate Stober Mar 28, 2024 MG Articles Webinar Recap: Is It Safe to Exercise with Myasthenia Gravis? Sarah Wright, DO MS, joined us on March 20 to discuss a hot topic in the MG Community Read More
Scott Bejda Mar 21, 2024 Living with MG Stories The “Rocky of Rap Media” Takes on MG 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
Siobhain Carolan Mar 15, 2024 Our MG Voice Advocacy 2024 Rare Disease Week on Capitol Hill 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