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Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
December of 2020 started perfectly. I recently accepted my first job offer after completing my undergraduate degree and anticipated my start date in the new year… In the second week […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Shekita Green and I have neuromyelitis optica. I am the mother of two teenagers, the wife of an Army vet and an entrepreneur. In my “past life”, […]
Read MorePosted by: The Sumaira Foundation in Caregiver, NMO, Voices of NMO
Jarrie grew up on a farm and declares himself a simple man. I think otherwise. I think Jarrie is a man for whom love is simply enough. Jarrie married his […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Shanice. I was born and raised in Jamaica and now reside in Toronto in Canada. I am a second-year medical student aspiring to be a physician in […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
September 21, 2021 — The Sumaira Foundation for NMO is pleased to welcome Stephanie Hamzo to its board of directors. Stephanie Hamzo With a true passion for patients, and dedication […]
Read MorePosted by: The Sumaira Foundation in NMO, Voices of NMO
My name is Mary Lou Gallegos. I was born and raised in San Antonio, Texas. I am the co-owner/founder of SA Perks L.L.C Detox Juices and Tonics. I am […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
August 16, 2021 – The Sumaira Foundation for NMO is pleased to welcome Elena Grebenciucova, MD to its medical advisory board. Elena Grebenciucova, MD Dr. Elena Grebenciucova is a neuro-immunologist […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On July 21, 2021, we gathered in person to celebrate 7 years of illuminating the darkness of neuromyelitis optica in Boston. With your support, we were able to raise over […]
Read MorePosted by: The Sumaira Foundation in NMO, Voices of NMO
My name is Allison and I am a married, busy mom of three children (17, 12 & 12 years old). My NMO journey started approximately seven years ago, when I […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
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 […]
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