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Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Back in 2013 and 2014, I completed two 100km walks to raise money for Oxfam – something I am so proud to have done! BUT in 2016, when I tried […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
August 23, 2019 – The Sumaira Foundation for NMO (TSF) and Connor B. Judge Foundation (CBJF) are proud to present Demystifying NMO, a podcast series aimed at simplifying scientific jargon associated […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Now that I have been diagnosed with Myelin Oligodendrocyte Glycoprotein Antibody-Associated disease, or MOG-Ab disease, I have met others who are afflicted and have listened to their stories. They all […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, TM, Voices of NMO
It all started when I was 20 years old – I went to urgent care because I was experiencing excruciating pain in my upper back to the point of tears. […]
Read MorePosted by: The Sumaira Foundation in Caregiver, NMO, Voices of NMO
This is a story of how a warrior is made. I have been gifted with the job of being this warrior’s mother and I am proud to share her story. […]
Read MorePosted 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 […]
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