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Posted by: The Sumaira Foundation in Uncategorized
The Sumaira Foundation Selects Citizen Health as Its Real-World Data Partner To Accelerate Neuroimmune Research and Provide an AI Teammate for Every Patient The partnership gives patients a next-generation AI […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
AFRICTRIMS Patient Day brings hope, education and community to sub-Saharan Africa. On May 29, 2026, history was made in Accra, Ghana, as patients, caregivers, healthcare professionals and advocates gathered at […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Voices of NMO
Aun no nos conocemos, pero estoy segura de que al final de esta lectura, quizá podamos conectar de alguna manera. Soy Ingrid pero puedes llamarme Inni y quiero compartir mi […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
The Sumaira Foundation is proud and pleased to welcome Dr. Fiifi Duodu, neurologist at Korle-Bu Teaching Hospital in Accra, Ghana, to join TSF’s international Medical Advisory Board as the first […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Le 31 mai 2026, des participants ont pris le départ des 20 km de Bruxelles aux couleurs de TSF. Un groupe de 28 participants s’est réuni autour d’une mission commune […]
Read MorePosted by: The Sumaira Foundation in Patient, Thyroid Eye Disease (TED), Voices of NMO
Je faisais le tour de l’Europe en camping-car avec mon conjoint depuis un an. Je venais de me lancer comme formatrice et nous voyagions : je n’avais jamais été aussi […]
Read MorePosted by: The Sumaira Foundation in Myasthenia Gravis (MG), Patient, Voices of NMO
In the world of elite distance swimming, success is built on a specific, predictable dialogue between the mind and the body. As a miler ranked at the top of the […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
In April, the team at Oxford University hosted their annual patient day for NMOSD and MOGAD patients and caregivers at the Aston Conference Centre. Rue and Jaycee – both NMOSD […]
Read MorePosted by: The Sumaira Foundation in MOGAD, Patient, Voices of NMO
At 26, my life felt like it was coming together. I was a young professional, full of energy, building my career and enjoying life in the city. I spent a […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
Just a few months ago I was diagnosed with NMOSD—and my life changed over night. Before that, I was an Ironman in training. I was two months away from my […]
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