Latest Post A Danish Musician’s Battle with Myasthenia Gravis Mika Filborne | September 19, 2024 A Danish Musician’s Battle with Myasthenia Gravis. Read More
Living with MG Stories Our MG Story: When Your Child Has Myasthenia Gravis Motunrayo Ononuga | June 6, 2024 The Oronuga family’s life was turned upside down when Teniola was diagnosed with MG at age three. They share what it is like to battle this chronic autoimmune condition in Nigeria. Read More
Community Fundraising Our MG Story: The Stehlik Sisters Give Back in Memory of Their Pops Kate Stober | June 4, 2024 An MG diagnosis leads to a passion for raising awareness and giving back. 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