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
Kate Stober Feb 23, 2023 Events MG patients discuss finding community at the MGFA Patient Conference Hear from patients about why they are attending the MGFA National Patient Conference in 2023. Read More
Nancy Law Apr 06, 2021 Events Only 6 More Days Until the MGFA National Conference – and I Can Hardly Wait! MGFA Board Chair Nancy Law Talks about her National Conference Memories and the Importance of this Annual Global Event. Read More