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Posted by: The Sumaira Foundation in NMOSD, ON, Patient, Transverse Myelitis (TM), Voices of TSF
I can trace my first NMO symptoms back to when I was just 12 years old… I’d be walking down a flight of stairs and for a split second, it […]
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Posted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
My name is Letitia and I am a 22-year-old South African NMO patient. My story began on the 26th of December 2017, Boxing Day… I had been suffering with an […]
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Posted by: The Sumaira Foundation in NMOSD, ON, Patient, Transverse Myelitis (TM), Voices of TSF
Hello, my name is James. I am 24 years old. I am a recent college graduate, a skateboarder, a geek, a lucky dude with an amazing family and friends. If […]
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Posted by: The Sumaira Foundation in Caregiver, Transverse Myelitis (TM), Voices of TSF
Addison “Addie” Havens was a healthy two year-old little girl full of energy and spunk who loved to play with her big brother… The weekend of January 29, 2016 began […]
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Posted by: The Sumaira Foundation in News & Announcements
FUNDING OPPORTUNITY ANNOUNCEMENT In 2020, TSF will be awarding up to 4 research grants, each with a maximum award of $25,000. Frequently Asked Questions Who is eligible for the grant […]
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Posted by: The Sumaira Foundation in NMOSD, Patient, Transverse Myelitis (TM), Voices of TSF
I was 33 years old in 1993, when I experienced a sudden attack of optic neuritis, an inflammation that damages the optic nerve causing vision loss. A small black dot, […]
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Posted by: The Sumaira Foundation in News & Announcements
December 16, 2019 — The Sumaira Foundation for NMO (TSF) and The Elliot Lewis Center are pleased to announce their partnership as of December 2019. The organizations have a shared […]
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Posted by: The Sumaira Foundation in News & Announcements
The theme for Gala 2020 is “old Hollywood” in celebration of the premiere of our 5-year impact video! We’ve set an ambitious goal to raise $100,000 to fund innovative, […]
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Posted by: The Sumaira Foundation in NMOSD, ON, Patient, Transverse Myelitis (TM), Voices of TSF
I have a rare, chronic neurological disease that affects my central nervous system. It’s caused me to become temporarily half-blind and feel throbbing pain everywhere… I was diagnosed with Neuromyelitis […]
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Posted by: The Sumaira Foundation in NMOSD, Patient, Voices of TSF
Imagine this: You’re driving on a highway, and suddenly, your hands stop working completely. You can’t grip the wheel. Imagine the terror and the confusion… And then imagine, that, thank […]
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