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Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
¿Alguna vez has tenido uno de esos sueños en los que, por más que corres, no avanzas? Bueno, pues así es como me he sentido durante los últimos tres años. […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
It was October 2019, I was a young mom at 25 years old toting around a toddler and an infant, and had my hands full in the most beautiful and […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
In 2022, my life took an unexpected turn. It all began with a high fever that started on August 31st and lasted for a week. At the time, I was […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Me llamo Olga Doncel, tengo 40 años y en este pequeño escrito voy a contar la historia de cómo, sin poder hacer nada, mi vida se partió en dos. Desde […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Until my early 30’s I was an active young woman, healthy, exercised regularly, independent, worked full time and loved to travel. I bought a three level townhome, had my own […]
Read MorePosted by: The Sumaira Foundation in Caregiver, NMO, Voices of NMO
My name is Roberto and I am a practicing attorney in Barcelona. When I think back to my childhood, one of my clearest memories is chasing my older sister, Rafaela, […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
September 2021 marked the perfect storm for NMO – a combination of a long-term infection and a viral illness. During the peak of the COVID lockdown on September 1, 2021, […]
Read MorePosted by: The Sumaira Foundation in Caregiver, MOG, Voices of NMO
Mi nombre es Ángela Sánchez Berrio, y quiero compartir con ustedes la historia de mi hijo Tomás Morales Sánchez, con la esperanza de encontrar empatía, apoyo y, sobre todo, visibilizar […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My journey began in 2013 when I was 11 years old. I was experiencing severe symptoms of neuromyelitis optica spectrum disorder, but I wasn’t diagnosed for a number of years. […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Rashmi and I have been living with NMOSD since 2015. I’m sharing my story with all of its ups and downs, tears and smiles, but most importantly, […]
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