Understanding the Canadian NMOSD Journey
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 advocates in which a variety of disease-related topics will be discussed. Our premiere webinar will feature the nation’s first NMOSD patient who successfully gave birth… Read More
2020 Grant Recipients
November 9, 2020 – We are proud to announce the grant recipients of TSF’s 2020 research grants. Congratulations to our recipients who received $25,000 to initiate their projects! Diagnostics in NMOSD Farrah Mateen, MD, PhD | Massachusetts General Hospital (Boston, MA) Aim: To pilot a novel point-of-care dry blood spot diagnostic test for patients with… Read More
NMOSD / MOG-AD Support Groups & Pages
August 18, 2020 – The Sumaira Foundation for NMO is pleased to present NMOSD / MOG-AD Support Groups & Pages Our team hopes that this document will serve as a valuable resource to our small but mighty community! A clickable PDF version is available. Simply click the yellow call-to-action button that reads, Support Groups & Pages,… Read More
Welcome Dr. Stacey Clardy!
July 29, 2020 – The Sumaira Foundation for NMO is pleased to welcome Stacey Clardy, MD, PhD to its medical advisory board. Stacey Clardy, MD, PhD Dr. Clardy is Associate Professor of Neurology with tenure at the University of Utah in the Division of Neuroimmunology within the Department of Neurology and Staff Neurologist at the… Read More
Celebrating 6 Years of TSF
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 at 12 PM EST. as our hosts Gaetano Morello and Lauren Michaels facilitate a thoughtful program featuring commentary from TSF’s founder Sumaira and medical members… Read More