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Posted 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 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
On July 28, 2022, TSF was joined by 100 friends of the Foundation to celebrate 8 years of illuminating the darkness of NMOSD and MOGAD at The Envoy Hotel’s Lookout […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
BOSTON, MA, August 4, 2022 – The Sumaira Foundation (TSF), a nonprofit organization focused on the rare neuroimmune diseases of NMOSD and MOGAD, is pleased to announce that it is […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
WASHINGTON, May 26, 2022—The PAN Foundation and The Sumaira Foundation (TSF) today announced they are launching a new partnership to help people living with neuromyelitis optica spectrum disorder (NMOSD), providing […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
February 10, 2022 – The Sumaira Foundation is pleased to welcome Dr. Joachim Havla of LMU Klinikum (Ludwig Maximilian University of Munich) as the first neurologist from Germany to join […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
December of 2020 started perfectly. I recently accepted my first job offer after completing my undergraduate degree and anticipated my start date in the new year… In the second week […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Hali and I am a 19 year old Scottish Law student living with NMOSD. — It all began in August 2021 when I developed a rash on […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 21, 2022 – The Sumaira Foundation is pleased to welcome Pr. Jacqueline Palace and Pr. Sarosh Irani from University of Oxford University to its Medical Advisory Board Jacqueline Palace, […]
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