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Posted 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 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 […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Hello! My name is Joyce and I am from Pittsburgh, Pennsylvania. My NMO symptoms started with loss of bladder control, stress inconvenience, irritable bowel with constipation, and sensation loss in […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
I’m Ilene, the youngest of seven children. I come from a family of school teachers and musicians. I love board games, musicals, plays, happy movies, skeet ball, Tower of Terror […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
The Sumaira Foundation for NMO (TSF) is proud to announce the launch of the TSF Ambassador Program by introducing the inaugural ambassador, Phil Tucker. Phil is an NMO warrior from […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
On Monday morning, Pam had a headache. For a woman who never got headaches, this was notable. In addition, when she turned her eyes right and left, she experienced eye […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Jamie was diagnosed with Non-Hodgkins Lymphoma at the age of 35. Her condition was such that she didn’t need treatment, just monitoring. She was even healthy enough to have a […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
My entire life, I was always a healthy and energetic person… I have played tons of sports and never went to the doctor unless it was for a sports physical. […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Sumaira’s NMO Story From the Transverse Myelitis Association blog, In Their Own Words (October 4, 2018) My name is Sumaira and I am the founder and executive director of The Sumaira Foundation […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
NEWS FLASH! The 3rd NMO Awareness Gala is featured in the latest edition of Improper Bostonian Magazine’s “Proper Bostonians” section! Thank you Dana Bisbee and friends at Improper Bostonian for helping us illuminate […]
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