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Posted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
Until my early 30’s I was an active young woman, healthy, exercised regularly, independent, worked full time and loved to travel. I bought a three level townhome, had my own […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On Saturday, August 16, 2025, TSF hosted a Patient Day in Salt Lake City for Rare Neuroinflammatory Disorders in collaboration with the University of Utah Health at University of Utah […]
Read MorePosted by: The Sumaira Foundation in Caregiver, NMOSD, Voices of NMO
My name is Roberto and I am a practicing attorney in Barcelona. When I think back to my childhood, one of my clearest memories is chasing my older sister, Rafaela, […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On the 20th of August, Clarinda Cerejo and Rashmi, TSF Ambassadors of India, attended the Rare Diseases Conference 2025, organized by the Federation of Indian Chambers of Commerce and Industry […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On July 26th, 2025, TSF hosted a Patient Day in Chicago for Rare Neuroinflammatory Disorders in collaboration with the Chicago MS Alliance at Rush University Medical Center’s Searle Conference Center. […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
August 25, 2025 — The Sumaira Foundation is pleased to welcome Dr. Dalia Rotstein, neurologist specialized in multiple sclerosis (MS) and other demyelinating diseases to join TSF’s international Medical Advisory Board […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Agosto, 18 2025 – The Sumaira Foundation (TSF) le da la bienvenida a Johanna Cardona a nuestro equipo como Coordinadora de embajadores Latino América. Para Agosto de 2025, la fundación […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
August 11, 2025 – The Sumaira Foundation (TSF) is pleased to welcome Randi Griffin to our team as a research associate. Randi brings 6+ years of clinical research experience in […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
September 2021 marked the perfect storm for NMO – a combination of a long-term infection and a viral illness. During the peak of the COVID lockdown on September 1, 2021, […]
Read MorePosted by: The Sumaira Foundation in Caregiver, MOGAD, Voices of NMO
Mi nombre es Ángela Sánchez Berrio, y quiero compartir con ustedes la historia de mi hijo Tomás Morales Sánchez, con la esperanza de encontrar empatía, apoyo y, sobre todo, visibilizar […]
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