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Posted by: 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 […]
Read MorePosted by: 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 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
The Sumaira Foundation for NMO presents NMO Wellness Day sponsored by Alexion Pharmaceuticals, Inc. and B.GOOD. Join us on June 22, 2019 at Spaulding Rehabilitation Hospital for a day of education […]
Read MorePosted by: The Sumaira Foundation in Caregiver, MOG, Patient, Voices of NMO
Published May 1, 2019
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Before I begin, I would like to thank you and tell you how much I appreciate you taking the time to read about my journey with neuromyelitis optica. Prior to […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
According to all of his medical tests, Greg is negative for both multiple sclerosis (MS) and neuromyelitis optica (NMO). Like many people misdiagnosed due to similar symptoms, Greg was considered […]
Read MorePosted 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 […]
Read MorePosted by: 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 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On February 9, 2019, Barre Groove hosted TSF’s first-ever charity event, POM for NMO, to raise awareness and money for neuromyelitis optica. We raised over $500, got a killer workout, and 10 […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
I was a 26 year old working in the Pentagon in the Navy Executive Dining Facility. I was Active Duty Navy for almost 8 years… On October 18, 2017, I […]
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