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Living with Autoimmune Encephalitis: Patient & Caregiver Perspectives
Автор: The Sumaira Foundation
Загружено: 2025-11-12
Просмотров: 33
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We were joined by patients and caregivers impacted by autoimmune encephalitis (AE) who shared their experiences with diagnosis, treatments, support and advocacy. This panel was moderated by Meg Poe, Executive Director of the Autoimmune Encephalitis Alliance.
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On October 18th, 2025, TSF hosted a Patient Day for Rare Neuroimmune Disorders in Seattle in collaboration with the UW Medicine Neurosciences Institute, Swedish Neuroscience Institute and in partnership with Autoimmune Encephalitis Alliance and The Stiff Person Syndrome Research Foundation.
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