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Posted 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 […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Hello. Hola. My name is Marie and I am proud to be the Welcome Manager for The Sumaira Foundation. I was diagnosed with NMO in 2007 when I was only […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Professional, Voices of NMO
Three years ago, right in the middle of my medical internship, I was diagnosed with Seronegative NMOSD. I took a leave of absence, not knowing if I could go back […]
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