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Posted by: The Sumaira Foundation in
The Human Collective Project (HCP) is TSF’s support group meetings offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
Read MorePosted by: The Sumaira Foundation in
The Human Collective Project (HCP) is TSF’s support group meetings offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
Read MorePosted by: The Sumaira Foundation in
The Human Collective Project (HCP) is TSF’s support group meetings offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
Read MorePosted by: The Sumaira Foundation in
The Human Collective Project (HCP) is TSF’s support group meeting offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
Read MorePosted by: The Sumaira Foundation in
The Human Collective Project (HCP) is TSF’s support group meetings offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
Read MorePosted by: The Sumaira Foundation in
The Human Collective Project (HCP) is TSF’s support group meetings offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 […]
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
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 […]
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