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Posted 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 […]
Read MorePosted by: The Sumaira Foundation in Caregiver, MOG, Voices of NMO
Ciao a tutti, mi presento, sono la mamma di Auri. Mi piace presentarmi così, perché questa è la sua storia, la storia di una bambina bella e forte che nel […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On Saturday, March 9, 2024, we hosted our New England Patient Day for NMOSD & MOGAD in Boston in collaboration with Dr. Michael Levy and Dr. Marcelo Matiello of Massachusetts […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
With a vulnerable yet advocational heart, I would love to re-introduce myself to the NMO community! My name is Alyson Tignor (née Pugh) and I am so much more than […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
March 7, 2024 — The Sumaira Foundation (TSF) is delighted to announce a new partnership during NMO and MS Awareness Months with We Are ILL, a nonprofit patient advocacy organization […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, TM, Voices of NMO
It all began in early 2020 when Kayla noticed a tingling sensation in her right leg. She didn’t think too much about it and figured it would go away. Thinking […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 26, 2024 — At TSF, we believe in the power of medical research for achieving breakthroughs toward better patient quality of life. In line with this ideology, many of […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 22, 2024 — The Sumaira Foundation is delighted to announce a new partnership with the Caminemos Foundation, a Mexican non-profit patient advocacy organization working in the area of demyelinating […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Les 16 et 17 décembre 2023, TSF France a organisé son premier événement présentiel à Paris. Plus de 40 patients et aidants de France, Belgique et Suisse nous ont rejoint […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
January 15, 2024 — The Sumaira Foundation is thrilled to announce Dr. Zhila Maghbooli, from the Multiple Sclerosis Research Center of Tehran University of Medical Sciences, Iran, as the first […]
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