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
Caroline Gayler Dec 14, 2022 Living with MG Stories Let’s Be Courageous, Together Priscilla Forrester’s courageous effort to connect community members and volunteer Read More
Caroline Gayler Apr 27, 2021 Stewardship Understanding How Your Impact Drives Change in the MG Community Our donors drive new research funding and community service and MGFA is demonstrating impact to our donors through stewardship. Read More