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Posted by: The Sumaira Foundation in News & Announcements
June 22, 2020 — The Sumaira Foundation for NMO is pleased to present its newest ambassadors to the TSF family. The ambassador team consists of 20 ambassadors who represent 15 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
March 31, 2020 — The Sumaira Foundation for NMO is pleased to present the results of the NMO community’s outreach efforts to have March declared “NMO Awareness Month” across the […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
The 4th Annual NMO Awareness Gala SATURDAY, MARCH 23, 2019 | DOORS OPEN AT 7:00PM MANDARIN ORIENTAL, GRAND BALLROOM (BOSTON, MA) You’re invited to our enchanted forest-themed annual event so […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, TM, Voices of NMO
I was diagnosed with Neuromyelitis Optica on July 25, 2015. My story is a little different than many of the stories I’ve heard or read about because my symptoms started […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Liz has had NMO for 25 years now. She’s only known it for ten… Since she’d had migraines throughout her childhood, Liz and her mother didn’t think too much […]
Read MorePosted by: The Sumaira Foundation in NMO, ON, Patient, TM, Voices of NMO
Meet Dionne, a vibrant 46-year old, former nurse, mother of 2 from New Orleans, Louisiana who has been living with NMO since 2009. Click below to watch Dionne share her […]
Read MorePosted by: The Sumaira Foundation in NMO, ON, Patient, TM, Voices of NMO
Meet Megan, a 16 year old NMO patient who and YouTube sensation (@PerfectlyKnitBeauty) who has been coping with her chronic illness through the use of makeup. We laud her courage, […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
I was diagnosed with NMO on March 10, 2015… An MRI that was done while I was receiving inpatient care for sudden paralysis of my lower limbs showed a spinal […]
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