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Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My story with neuromyelitis optica spectrum disorder (NMOSD) began in 2021, although at the time, I had no idea what was happening to me. It started with something subtle yet […]
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Nobody told me that retirement was going to be so challenging! I was ready to start enjoying the fruits of my labor, when the unexpected happened… As with all things […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 27, 2025 — The Sumaira Foundation is pleased to welcome Dr. Jeffrey Bennett, Professor of Neurology & Ophthalmology, from the University of Colorado School of Medicine to join TSF’s international […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Era maggio 2023 e mi stavo avvicinando sempre di più alla sessione estiva degli esami. Avevo molti progetti da consegnare, dormivo poco e mi sentivo molto stressata. Così decisi di […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Dr. Grace Gombolay, Sumaira Ahmed, Nell Choi, Alanna Yee, Nakeshia Nickerson and Tara Zier. On Saturday, July 20, 2024, the American Academy of Neurology (AAN) marked a historic milestone with […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On July 18, 2024, we were grateful and honored to celebrate 10 years of The Sumaira Foundation in Atlanta alongside physicians, community members, patients, supporters, and our TSF team. Our […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
14 de agosto de 2024 – A Fundação Sumaira (TSF) tem a honra de anunciar uma nova parceria com a Associação Brasileira de Neuromielite Óptica (ABNMO) que busca avançar na […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Much has changed in my world since my initial story had been published on TSF’s website in 2020. (scroll below to read the original piece) One of the more notable […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On Saturday, June 15, 2024, we hosted our Cleveland Patient Day for NMOSD & MOGAD in collaboration with Dr. Amy Kunchok, Dr. Mary Rensel and Dr. Justin Abbatemarco at Cleveland […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Je m’appelle Nelly, j’ai 44 ans et je vis dans un joli village dans l’Oise et j’ai la MOGAD. Sans le savoir cette maladie m’avait déjà fait un petit clin […]
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