Posted by: The Sumaira Foundation in NMO, Patient, TM, Voices of NMO
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 had a myriad of physical and mental illnesses throughout my whole life, which seemed to be getting worse as the years went on. My mother […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
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 MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Jamie was diagnosed with Non-Hodgkins Lymphoma at the age of 35. Her condition was such that she didn’t need treatment, just monitoring. She was even healthy enough to have a second child. After the birth, though, she was put on Rituximab for the lymphoma, once a week for four weeks. Two years later, one night […]
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