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Tag: neuromyelitis optica
Posted by:
The Sumaira Foundation
in News & Announcements
On June 22, 2019, The Sumaira Foundation for NMO hosted its inaugural NMO Wellness Day, a day-long community event oriented to foster discussions around health and wellness as they relate to […]
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The Sumaira Foundation
in Caregiver, NMO, Voices of NMO
Chelsey Judge, PhD, is a scientist with a particular interest in immunology. She also happen to be the sister of an NMO patient. Chelsey shares her Voices of NMO™ story […]
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Posted by:
The Sumaira Foundation
in News & Announcements
June 21, 2019 – We are proud to announce the 2019-2020 TSF Ambassadors! The ambassadors represent the Foundation’s brand, helping to lead the TSF for NMO mission and movement in […]
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The Sumaira Foundation
in NMO, Patient, Voices of NMO
April Fools’ Day jokes are supposed to be funny. However, the one my parents thought I was playing two years ago, was most definitely not. I’m not pulling your leg […]
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Posted by:
The Sumaira Foundation
in News & Announcements
June 5, 2019 – The Sumaira Foundation for NMO is pleased to welcome Michael Levy, MD, PhD, and Tamara B. Kaplan, MD, to its medical advisory board. Michael Levy, MD, […]
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The Sumaira Foundation
in NMO, ON, Patient, Voices of NMO
In February 2019, I received an NMOSD diagnosis after nearly 11 years of being treated for multiple sclerosis… I think when you are diagnosed with a chronic disease, knowing who […]
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The Sumaira Foundation
in NMO, Patient, Voices of NMO
Is it unreasonable to call a woman who comes down with a rare autoimmune disease lucky? What about two autoimmune diseases? It may seem strange, but Eleanor considers herself lucky. […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, Voices of NMO
Greetings Everyone, I’m Shiela Marie Sta. Maria Rutaquio, from Binangonan, Rizal 1940 Philippines, who have this rare and incurable autoimmune disease called NMOSD (NEUROMYELITIS OPTICA SPECTRUM DISORDER), a demyelinating disease […]
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The Sumaira Foundation
in MOG, NMO, Professional, Voices of NMO
Like many physician-researchers in my field, I spend a lot of time thinking about NMO, both inside and outside of the clinic. The science of NMO is fascinating to me […]
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Posted by:
The Sumaira Foundation
in NMO, ON, Patient, Voices of NMO
My NMO story started about 15 years ago. I was a sophomore in high school and was just released for summer break… The very next day, I started to feel […]
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