Shannon Murray Jun 27, 2024 MG Articles Managing a Pregnancy When You Have Myasthenia Gravis: My MG Story Read how Shannon is navigating her new MG diagnosis alongside her pregnancy. Read More
Siobhain Carolan Mar 15, 2024 Our MG Voice Advocacy 2024 Rare Disease Week on Capitol Hill Siobhain Carolan, who lives with congenital myasthenic syndrome, discusses her experiences advocating for those with rare diseases at 2024 Rare Disease Week on the Hill. Read More
Siobhain Carolan Mar 13, 2024 Living with MG Stories My CMS Journey: How the Right Diagnosis Changed My Life and Led Me to Advocacy Siobhain shares how living with congenital myasthenic syndrome helped her become a fierce advocate for those with rare diseases. Read More