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Posted 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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
My journey began in 2013 when I was 11 years old. I was experiencing severe symptoms of neuromyelitis optica spectrum disorder, but I wasn’t diagnosed for a number of years. […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On June 8th, 2025, TSF hosted a Patient Day for NMOSD & MOGAD in Washington DC in collaboration with Dr. Benjamin Osborne at the Georgetown University Conference Center (Thomas & […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
My name is Rashmi and I have been living with NMOSD since 2015. I’m sharing my story with all of its ups and downs, tears and smiles, but most importantly, […]
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