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Posted by: The Sumaira Foundation in Caregiver, NMOSD, Voices of TSF
J’ai toujours été très proche de ma mère. Quand j’étais petite elle m’emmenait partout : au parc, à la mer, faire du shopping, aller chez des amis. Elle travaillait de […]
Read MorePosted by: The Sumaira Foundation in Professional, Voices of TSF
The Beginning: A Question That Stayed With Me During my medical studies, in my fourth year at university, I remember preparing a final presentation during my neurology module. I chose […]
Read MorePosted by: The Sumaira Foundation in NMOSD, 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 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 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 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. […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
Before September 2024, my life was full of movement. I was the kind of person who rarely sat still – playing pickleball, skiing in the winter, walking my dogs. Willow […]
Read MorePosted by: The Sumaira Foundation in Myasthenia Gravis (MG), Patient, Voices of TSF
Mi chiamo Adalgisa, ho trent’anni e nel 2023 ho scoperto di avere la Miastenia Gravis: una malattia neuromuscolare cronica e autoimmune che provoca debolezza muscolare. Da quel momento penso sempre […]
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