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Patient
Posted by:
The Sumaira Foundation
in NMO, ON, Patient, Voices of NMO
My name is AnneMarie and my journey with NMO began in 2002 when I was just 16 years old… One April morning, I woke up with a stabbing pain in […]
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Posted by:
The Sumaira Foundation
in NMO, ON, Patient, Voices of NMO
My name is Jaime. I live in the small town of Exeter, Pennsylvania. I am a wife and a mother to a beautiful and healthy 15 year-old daughter. And I […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, TM, Voices of NMO
My biggest fear in life was that I would have some incurable sickness or disease. Not heights, nor spiders, nor public speaking. It was getting sick. Both of my parents […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
Today this is where I am – right here and right now. God has a plan, yesterday is gone and tomorrow may never be – It’s up to me as […]
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Posted by:
The Sumaira Foundation
in NMO, ON, Patient, TM, Voices of NMO
My name is Kellin. I am a 28-year-old South African NMO patient and this is my story… Late in 2015, my father suddenly passed away. It was a shock to […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
Freshman year of college is a time to form your sense of identity, but when I started school, I thought that forming this ‘new’ me meant dying my hair blue, […]
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Posted by:
The Sumaira Foundation
in NMO, ON, Patient, TM, Voices of NMO
My name is Mitchel Navarro. I’m 34 years old, a wife, and a proud momma to two beautiful children – a girl and a boy. I have a bachelors degree […]
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Posted by:
The Sumaira Foundation
in NMO, ON, Patient, TM, Voices of NMO
Sunday 15 December 2013, on a friend’s farm in the beautiful little town of Dullstroom in Mpumalanga South Africa, started as blissfully peaceful as it sounds. This was to change […]
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Posted by:
The Sumaira Foundation
in NMO, ON, Patient, TM, Voices of NMO
It started with a never-ending headache… Click the image below to watch Chasity’s video in which she describes her experience with optic neuritis. Although she has lost a significant amount […]
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Posted by:
The Sumaira Foundation
in NMO, ON, Patient, TM, Voices of NMO
I can trace my first NMO symptoms back to when I was just 12 years old… I’d be walking down a flight of stairs and for a split second, it […]
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