Kate Stober Sep 21, 2023 Our MG Voice Advocacy For the Golden-Gershwins, Annual Golf Tournament is a Family Affair For 31 years, the Helen and Leonard A. Golden Memorial Golf Classic has brought together family, friends, neighbors, and colleagues to raise funds for myasthenia gravis research. Read More
Meena Outlaw Jun 29, 2023 Living with MG Stories My MG Story – I Persevere Because There’s Hope What I want others to know after nearly a decade with MG. Read More
Sam Lam Jun 22, 2023 Living with MG Stories My MG Story: Balancing MG with Life, Work, and Friends I hope my story can help folks, especially younger patients, feel that they are not alone. Read More
Nick Patrone Jun 15, 2023 Living with MG Stories Better Together: We Share a Myasthenia Gravis Diagnosis How two people living with myasthenia gravis found each other. Read More
David Waters Jun 08, 2023 Living with MG Stories Caregiving: The Struggle is Real caregiver Navigating the complex journey of caring for your spouse – and remembering to care for yourself. Read More
Kate Stober Jun 01, 2023 Living with MG Stories Miss America Program Titleist Audrey Getman Doesn’t Let MG Stop Her Miss Kingston Audrey Getman shares her MG story. Read More
Kate Stober May 25, 2023 Living with MG Stories Tips for Traveling with Myasthenia Gravis Traveling with an illness like myasthenia gravis can be challenging, but with some planning and the right tricks up your sleeve, you can enjoy your trip safely. Read More
Christina Aquila Apr 19, 2023 MG Articles Healthy Green Smoothies from MGFA nutrition Green smoothies give you a dose of veggies with your fruit and are a great way to start the morning or provide an afternoon snack. People with MG may find that smoothies are an easier way to ensure you receive healthy, nutritious foods even when you are having difficulty chewing and swallowing. Read More
Kate Stober Apr 13, 2023 Events MGFA National Patient Conference Brings MG Community Together See photos and watch session recordings from our first in-person patient conference since 2019. Read More
Kate Stober Apr 04, 2023 MG Research Pediatric MG: Listen to This Podcast Episode Our MG Voice Advocacy, Medical Professionals, Living with MG Stories MGFA’s Meridith O’Connor talks with Dr. Jonathan Strober, director of the Neuromuscular Clinic at Benioff Children’s Hospital. Read More
Kate Stober Mar 02, 2023 Our MG Voice Advocacy Rare Disease Week: Highlighting Seronegative MG, a “Rare-of-the-Rare” Disease seronegative The struggle seronegative myasthenia gravis patients face for diagnosis and treatment. Read More