Kathalina Nguyen Aug 08, 2024 Living with MG Stories Back to Doing What I Love: My Myasthenia Gravis Story How a clinical trial brought back my smile 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