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Posted by: The Sumaira Foundation in News & Announcements
Les 23 et 24 novembre 2024, The Sumaira Foundation France a tenu son deuxième week-end patients et aidants à Paris. Cet événement était en collaboration avec MIRCEM. Durant ces deux […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Back in July 2022, I was fully immersed in motherhood with my two daughters approaching toddlerhood, finally feeling like I was finding my footing in my career after COVID. Life […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
December 11, 2024 — The Sumaira Foundation is pleased to welcome Dr. Eoin Flanagan from the Mayo Clinic in Rochester, Minnesota, to join TSF’s international Medical Advisory Board. Eoin P. Flanagan, […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
In 2019, I discovered a surprising new passion for running, completing 35 5Ks in 35 weeks and finding it to be an unexpected and rewarding outlet. But just a year […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
December 3, 2024 – The Sumaira Foundation (TSF) is pleased to welcome Letitia Annamalay to our leadership team as International Ambassador Liaison. Letitia will be overseeing TSF’s Ambassador Program in […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
It was December 27, 2022, two days after a quiet but emotionally stressful Christmas in India when I noticed a blurry white spot in my left eye which showed up […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
November 8, 2024 — The Sumaira Foundation is pleased to welcome Dr. Ho Jin Kim of the National Cancer Center in South Korea to join TSF’s international Medical Advisory Board. Dr. […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Am 02.10.2024 fand unter Federführung der Forschungsgruppe NEMOS in den Räumlichkeiten des Landessportbundes Hessen in Frankfurt der PatientInnentag für Betroffene von NMOSD und MOGAD statt. Bereits am Vorabend nutzten viele […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Je m’appelle Rokhaya Gningue, maman d’un beau jeune homme de 18 ans. Originaire du Sénégal, je réside actuellement au Québec. En 2009, j’ai reçu un diagnostic de sclérose en plaques, […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On Saturday October 5, 2024, we hosted our Miami Patient Day for NMOSD & MOGAD at Margaritaville Hollywood Beach Resort. Our in-person bilingual (english & spanish) event hosted 65+ attendees […]
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