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
Meridith O’Connor Feb 25, 2023 Our MG Voice Advocacy When Every Day is Rare Disease Day Illuminating the support rare disease patients need 365 days of the year. Read More