Posted by: The Sumaira Foundation in
Los cuidadores de personas con condiciones neuroinmunes raras como NMOSD y MOGAD necesitan un espacio para contar sus experiencias. Este espacio para cuidadores es dirigido por un cuidador de Colombia […]
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Posted by: The Sumaira Foundation in Caregiver, NMOSD, Professional, Voices of NMO
I am a caregiver to my daughter, Nell, who was diagnosed with NMO at age 9. Prior to her diagnosis, she was an active, vibrant girl playing travel lacrosse, robustly […]
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Posted by: The Sumaira Foundation in NMOSD, Patient, Voices of NMO
My name is Letitia and I am a 22-year-old South African NMO patient. My story began on the 26th of December 2017, Boxing Day… I had been suffering with an […]
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