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Posted by: The Sumaira Foundation in Caregiver, NMO, Voices of NMO
Modern medicine in the United States was a complete failure. For six weeks, the hospitals, doctors, and many lab tests couldn’t piece a single clue together… It was 2018, and […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
28 février 2023 – The Sumaira Foundation (TSF) annonce la création et le lancement de TSF France, apportant un soutien supplémentaire indispensable à la communauté française touchée par la NMO […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Els is ambassadeur voor de Sumaira Foundation, die opkomt voor de belangen van mensen met NMOSD en MOGAD. Zelf kreeg ze begin 2022 de diagnose van NMOSD. Ik werd in […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Bonjour à tous, je m’appelle Fatiha. J’habite à Étalleville en Normandie. Je suis tombée malade le 20 février 2016. Date anniversaire de la mort de mon père. Double peine pour […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 3, 2023 — The Sumaira Foundation is pleased to welcome Fabienne Brilot, PhD, of the University of Sydney (Australia) to join TSF’s medical advisory board. Fabienne Brilot, PhD Professor […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 3, 2023 — The Sumaira Foundation is pleased to welcome Dr. Sudarshini Ramanathan of the University of Sydney (Australia) to join TSF’s medical advisory board. Sudarshini Ramanathan, BSc (Med) […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 3, 2023 — The Sumaira Foundation is pleased to welcome Patrick Waters, BSc PhD CSci FIBMS FRCPath, of the University of Oxford (United Kingdom) to join TSF’s medical advisory […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
December 21, 2022 — The Sumaira Foundation is pleased to announce the first round of awardees of TSF’s 2022 research grants. Congratulations to all the researchers who will each be awarded […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Le 6 octobre 2014, le jour où ma vie a pris une nouvelle voie pour poursuivre son chemin. Le jour où j’ai commencé une cohabitation avec une maladie rare… À […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Hello fellow NMO sisters and brothers. My name is Roxana aka “Roxy”. I was diagnosed with NMO in June 2011 when I was 17 years old. The first symptom I […]
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