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Posted by: The Sumaira Foundation in Caregiver, NMO, Voices of NMO
Neuromyelitis Optica – a rare disease that appeared out of the blue and had a mission to suck the life out of my dear sister. At first we thought that […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Join us for an evening of cocktails, networking and awareness of Neuromyelitis Optica on Thursday, August 20th at the monumental Empire State Building. The ticket cost will cover entry, drinks, […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
The Sumaira Foundation is now on AmazonSmile! You shop and Amazon gives. Amazon donates 0.5% of eligible purchases to a charitable organization you choose to support. Shop the same products […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
We hosted our 1st fundraiser on Sunday, February 8th 2015 at the beautiful ROW34 in Fort Point, Boston. It was a major success with 50 guests in attendance despite the […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
I was 7 years old and after a normal school day, I noticed blurred vision in my left eye. As a very active and healthy child, this was unusual and […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
It began like a pain unlike any other. In 2009, and during my sophomore year of college, I was sitting in class when the shooting pain down my back began. […]
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