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Posted by: The Sumaira Foundation in NMOSD, Patient, Transverse Myelitis (TM), Voices of TSF
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 NMOSD, Patient, Voices of TSF
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 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, Patient, Transverse Myelitis (TM), Voices of TSF
My biggest fear in life was that I would have some incurable sickness or disease. Not heights, nor spiders, nor public speaking. It was getting sick. Both of my parents […]
Read MorePosted by: The Sumaira Foundation in NMOSD, ON, Patient, Transverse Myelitis (TM), Voices of TSF
My name is Kellin. I am a 28-year-old South African NMO patient and this is my story… Late in 2015, my father suddenly passed away. It was a shock to […]
Read MorePosted by: The Sumaira Foundation in MOGAD, NMOSD, Professional, Transverse Myelitis (TM), Voices of TSF
Maureen is a nurse. She worked in neurocritical care at Johns Hopkins Hospital for many years before she had ever heard of NMO. But in 2007, shortly after Dr. Benjamin […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Although we would prefer to get together in person, we look forward to coming together virtually in October to commemorate six years of TSF. Please join us on Saturday, October 24 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, ON, Patient, Transverse Myelitis (TM), Voices of TSF
My name is Mitchel Navarro. I’m 34 years old, a wife, and a proud momma to two beautiful children – a girl and a boy. I have a bachelors degree […]
Read MorePosted by: The Sumaira Foundation in NMOSD, ON, Patient, Transverse Myelitis (TM), Voices of TSF
Sunday 15 December 2013, on a friend’s farm in the beautiful little town of Dullstroom in Mpumalanga South Africa, started as blissfully peaceful as it sounds. This was to change […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
June 22, 2020 — The Sumaira Foundation for NMO is pleased to present its newest ambassadors to the TSF family. The ambassador team consists of 20 ambassadors who represent 15 […]
Read MorePosted by: The Sumaira Foundation in NMOSD, ON, Patient, Transverse Myelitis (TM), Voices of TSF
It started with a never-ending headache… Click the image below to watch Chasity’s video in which she describes her experience with optic neuritis. Although she has lost a significant amount […]
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