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Posted 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 […]
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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 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 […]
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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 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
August 22, 2022 – The Sumaira Foundation is pleased to welcome Pr. Friedemann Paul of Charité – Universitätsmedizin Berlin (Germany) to join TSF’s medical advisory board. Pr. Friedemann Paul Friedemann Paul […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
I was born and raised in Cuba where I played outside, ran, and enjoyed time with my friends. In my healthy teen years, I didn’t think I’d ever become chronically […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
August 16, 2022 – The Sumaira Foundation (TSF) is please to announce a partnership with The Assistance Fund (TAF) to help people living in the US with neuromyelitis optica spectrum […]
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