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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 […]
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Posted 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 […]
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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 […]
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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) […]
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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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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 […]
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Posted 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 […]
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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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The Sumaira Foundation
in MOG, NMO, Professional, Voices of NMO
I was a young resident at the University of Verona’s, Neurology Unit when I met a woman with rapidly evolving extensive myelitis. I first thought about NMOSD and asked our […]
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The Sumaira Foundation
in MOG, NMO, Professional, Voices of NMO
It was over a decade ago, but I remember it like yesterday, the first patient I looked after with NMOSD. Actually, there were two of them in the same neuroimmunology […]
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