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Posted by: The Sumaira Foundation in MOG, NMO, Professional, Voices of NMO
The Beginning of the Dream: Why I Chose Neuroimmunology During my daily work as a clinical pathologist specializing in immunology at the Faculty of Medicine, Cairo University (Kasr Al-Ainy), I […]
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2018 started out great. I was a senior in high school, applying to universities and getting excited about high school prom. I was working at a fast food restaurant and […]
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Ghanaian-born and UK-raised, I was diagnosed with aquaporin-4 positive (AQ4+) neuromyelitis optica spectrum disorder (NMOSD) in May 2023, which was completely life-changing, to say the least! All of a sudden, […]
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Anfang 2021 fing alles mit einer starken Coronainfektion an, von der ich mich das ganze darauffolgende halbe Jahr nicht mehr erholte. Ich verlor viel Gewicht, fühlte mich schwach, hatte schlechte […]
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Mi nombre es Andrea, tengo 28 años y vivo con más de un huésped incómodo en mi cuerpo. Comencemos por el principio… una introducción no tan breve sobre mí. A […]
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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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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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