Latest Post What gives you hope? Kate Stober | November 14, 2025 The MG Community shares what keeps them going, despite the hardships of the disease. Read More
Living with MG Stories MG Articles Managing a Pregnancy When You Have Myasthenia Gravis: My MG Story Shannon Murray | June 27, 2024 Read how Shannon is navigating her new MG diagnosis alongside her pregnancy. Read More
MG Articles Beating the Heat During Summer Months Kate Stober | June 20, 2024 Many people with myasthenia gravis will tell you symptoms flare up during the summer months. Here are a few tips to help you manage MG in hot weather. 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