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Posted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
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, […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
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 NMOSD, Patient, Voices of NMO
With a vulnerable yet advocational heart, I would love to re-introduce myself to the NMO community! My name is Alyson Tignor (née Pugh) and I am so much more than […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Transverse Myelitis (TM), Voices of NMO
It all began in early 2020 when Kayla noticed a tingling sensation in her right leg. She didn’t think too much about it and figured it would go away. Thinking […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
Hello. Hola. My name is Marie and I am proud to be the Welcome Manager for The Sumaira Foundation. I was diagnosed with NMO in 2007 when I was only […]
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