Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
I was diagnosed with Neuromyelitis Optica Spectrum Disorder (NMOSD) in November 2013. My symptoms started June of that year with my toes going numb, shortly after returning from a cruise […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
My name is Ashlee. Thank you for taking the time to read my story. I’m not really sure where to begin and I’ve never publicly shared my NMO story before […]
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Posted by:
The Sumaira Foundation
in Caregiver, NMO, Voices of NMO
Neuromyelitis Optica – a rare disease that appeared out of the blue and had a mission to suck the life out of my dear sister. At first we thought that […]
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