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Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Hali and I am a 19 year old Scottish Law student living with NMOSD. — It all began in August 2021 when I developed a rash on […]
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January 21, 2022 – The Sumaira Foundation is pleased to welcome Pr. Jacqueline Palace and Pr. Sarosh Irani from University of Oxford University to its Medical Advisory Board Jacqueline Palace, […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
You are invited to attend TSF’s old Hollywood-themed 5th NMO Awareness Gala Saturday, March 26, 2022 at 7 PM Mandarin Oriental, Boston We’ve set an ambitious goal to raise $250,000 […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Christy and I’ve been fighting this disease without knowing what I was up against since before 2008… I started calling this thing my “venom” because it reminded […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
December 1, 2021 — The Sumaira Foundation is proud to announce the grant recipients of TSF’s 2021 SPARK and Unicorn grants. Congratulations to our 5 recipients who each received $25,000 […]
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November 22, 2021 – The Sumaira Foundation is pleased to welcome Professor Romain Marignier as the 1st international NMO specialist to join TSF’s medical advisory board. Romain Marignier, MD Pr. […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
February 16, 2021 – The Sumaira Foundation for NMO (TSF) is pleased to announce the Light the Way Forward Grant made possible by a research grant from Viela Bio. Viela […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
November 25, 2020 — The Sumaira Foundation for NMO is pleased to present “Understanding the Canadian NMOSD Journey”, a 6-part live webinar series featuring Canadian patients, caregivers, clinicians, researchers, and […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, TM, Voices of NMO
On the evening of Sunday, 17th January 2010, my mother was putting up a fight with my brothers and I to go to bed while we were chasing each other […]
Read MorePosted by: The Sumaira Foundation in NMO, ON, Patient, Voices of NMO
My name is AnneMarie and my journey with NMO began in 2002 when I was just 16 years old… One April morning, I woke up with a stabbing pain in […]
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