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Posted by: The Sumaira Foundation in News & Announcements
WASHINGTON, May 26, 2022—The PAN Foundation and The Sumaira Foundation (TSF) today announced they are launching a new partnership to help people living with neuromyelitis optica spectrum disorder (NMOSD), providing […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOG-AD) In 2014, The Sumaira Foundation (TSF) launched to raise awareness of neuromyelitis optica spectrum disorder (NMOSD) and create a community of people brought together […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Clean and clear were my glasses but still I had trouble seeing clearly with my right eye. On Easter Monday in 2019, my vision deteriorated and by the end of […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
375 guests. $220K raised for research. 22 patients from 15 cities in 2 countries. On Saturday, March 26, 2022, 375 guests gathered for the 5th Annual NMO Awareness Gala at […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
A native Portuguese speaker and resident of Denmark, Leda wrote her story in English, Portuguese, and Danish. Please scroll down to read Leda’s story in Portuguese and/or Danish. In 2018 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
March 10, 2022 – The Sumaira Foundation (TSF) is pleased to announce the launch of “Imagine My Life With NMO,” a video series showcasing the experiences of people living with […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Part I and II of this story were originally published in 2015 by NMO Stories, presented by The Guthy-Jackson Foundation and the Connor B. Judge Foundation. It was shared again […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Pauline Richardson nee Grant. I grew up on a farm in Jamaica. My mom, being a cheerful giver, would invite people over all the time, always making […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Uncategorized, Voices of NMO
The bad news is that apparently I’m about to die. The good news is that both my fantasy doctor boyfriend and my ex-husband are at my bedside for this moment… […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
February 10, 2022 – The Sumaira Foundation is pleased to welcome Dr. Joachim Havla of LMU Klinikum (Ludwig Maximilian University of Munich) as the first neurologist from Germany to join […]
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