Latest Post A New Era for the MG Patient Registry: Empowering Patients, Advancing Research Kate Stober | October 28, 2025 MGFA is proud to announce the next stage in the evolution of the MG Patient Registry: the Vitaccess Real MG Registry. Read More
Living with MG Stories The Snowflake Disease Greg Olsen | June 17, 2024 Just like a snowflake, myasthenia gravis symptoms can appear one minute and be gone the next. Read More
Living with MG Stories Our MG Story: Advice for Spouses and Caregivers Kate Stober | June 13, 2024 In this vlog, Cary asks her husband Zack some questions about his experience as an MG caregiver. Read More
Living with MG Stories Something to Chew On Aimee Sears | June 10, 2024 How is MG like a piece of chewing gum? 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
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