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Posted 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 […]
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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, […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Bonjour, je m’appelle Natasha, j’ai 46 ans, et voici comment la NMOSD (neuromyélite optique) est entrée dans ma vie. Tout a commencé à l’été 2001. J’avais 23 ans et je […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Rita Ddungu Sembuya and I am from Kampala, Uganda. I am a patient living with neuromyelitis optica (NMO), and I was very pleased to receive an introduction […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My story with neuromyelitis optica spectrum disorder (NMOSD) began in 2021, although at the time, I had no idea what was happening to me. It started with something subtle yet […]
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