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Posted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Era maggio 2023 e mi stavo avvicinando sempre di più alla sessione estiva degli esami. Avevo molti progetti da consegnare, dormivo poco e mi sentivo molto stressata. Così decisi di […]
Read MorePosted 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 […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
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 […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
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 Nelly, j’ai 44 ans et je vis dans un joli village dans l’Oise et j’ai la MOGAD. Sans le savoir cette maladie m’avait déjà fait un petit clin […]
Read MorePosted by: The Sumaira Foundation in Caregiver, MOG, Voices of NMO
Ciao a tutti, mi presento, sono la mamma di Auri. Mi piace presentarmi così, perché questa è la sua storia, la storia di una bambina bella e forte che nel […]
Read MorePosted by: The Sumaira Foundation in Caregiver, MOG, Voices of NMO
Drogi Czytelniku – chciałabym podzielić się z Tobą naszą bardzo osobistą historią, która zmieniła życie moje i mojego męża. Bardzo bym chciała, żeby nasza historia była dla Ciebie przykładem nadziei […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
On Monday, I woke up with a slight ache on the left side of my lower back which felt numb, like a bruise but without the pain. This numb spot […]
Read MorePosted by: The Sumaira Foundation in MOG, NMO, Professional, Voices of NMO
I was a young resident at the University of Verona’s, Neurology Unit when I met a woman with rapidly evolving extensive myelitis. I first thought about NMOSD and asked our […]
Read MorePosted by: The Sumaira Foundation in MOG, NMO, Professional, Voices of NMO
It was over a decade ago, but I remember it like yesterday, the first patient I looked after with NMOSD. Actually, there were two of them in the same neuroimmunology […]
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