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Posted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Desde los 13 años he practicado deporte de alto rendimiento, pasando por el futbol soccer profesional, correr medias distancias y realizar triatlones hasta completar un IRONMAN 140.6, siempre he tenido […]
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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 […]
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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 […]
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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 […]
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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, […]
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I am Zoe and I am from Cyprus aka I am a Greek Cypriot. I had no health issues at all until 2020 when I was 50 years old… In […]
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Much has changed in my world since my initial story had been published on TSF’s website in 2020. (scroll below to read the original piece) One of the more notable […]
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Hola ¿Tienes 2 minutos? Déjame contarte parte de mi historia. Esta comienza con el recuerdo de mi abuelo, él solía decir que todos tenemos una misión en la vida. Para […]
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It all began in June 2020, the peak of when COVID-19 had finally hit Texas… Allow me to backtrack before I began with my symptoms for a bit: I have […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
On January 30, 2023, I was diagnosed with relapsing-remitting multiple sclerosis following the onset of nearly complete vision loss in my left eye. That day marked a profound turning point […]
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