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Posted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
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 TSF
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 TSF
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 TSF
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 TSF
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 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Am Samstag, den 7. März 2026, veranstaltete TSF in Zusammenarbeit mit Prof. Friedemann Paul an der Charité Berlin einen Patiententag für seltene neuroimmunologische Erkrankungen. Bei unserer Präsenzveranstaltung durften wir über […]
Read MorePosted by: The Sumaira Foundation in MOGAD, Patient, Voices of TSF
La MOGAD est entrée dans ma vie sans prévenir. Au début, c’était presque rien. Une petite tache noire dans mon œil droit, en mai 2022. Je pensais que ça passerait. […]
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