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Posted by: The Sumaira Foundation in Autoimmune Encephalitis (AE), Patient, Voices of TSF
In 2023, I was preparing to go to Washington, DC for Rare Disease Week as a Young Adult Rare Representative (YARR) with the EveryLife Foundation for Rare Diseases. I had […]
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Con motivo del Día Mundial de la Encefalitis 2026, nos complace contar con la participación de la Dra. Nicole Somerville Briones, quien ofrecerá una visión general de la encefalitis autoinmune […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Il 18 novembre 2023 TSF Italia ha ospitato la sua prima giornata internazionale dedicata ai pazienti in Italia, a Verona. Si sono uniti a noi 50 pazienti, operatori sanitari e […]
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