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Posted by: The Sumaira Foundation in News & Announcements
On July 24, 2019, we honored 5 years of TSF for NMO and celebrated 30 years of founder + executive director, Sumaira, at ROW 34. 62 guests gathered in pink […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
She thought it might be her fault. After all, she was working 14-hour days driving a truck, going to school full time and caring for a young son on her […]
Read MorePosted 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 […]
Read MorePosted by: 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 […]
Read MorePosted 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 […]
Read MorePosted 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 […]
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