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
Partnership | TSF x NICA
July 13, 2020 — The Sumaira Foundation for NMO (TSF) and the National Infusion Center Association (NICA) are pleased to announce their partnership as of July 2020. The Sumaira Foundation for NMO (TSF) is a 501(c)(3) organization founded by an NMO patient, and is dedicated to generating global awareness of neuromyelitis optica spectrum disorder (NMOSD), fundraising… Read More
Ignition Survey Results – MOG-AD Treatment Practices
July 9, 2020 — In spring 2020, The MOG Project partnered with the SRNA and The Sumaira Foundation to understand treatment practices among MOG-AD patients. The goal of the survey was to learn from the MOG-AD community experience and share results with physicians and each other. 267 MOG-AD patients and their caregivers completed a survey… Read More