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Spanish Posted by: The Sumaira Foundation in News & Announcements
August 18, 2020 – The Sumaira Foundation is pleased to present NMOSD/MOG-AD Support Groups & Pages Our team hopes that this document will serve as a valuable resource to our […]
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November 13, 2019 – The Sumaira Foundation for NMO (TSF) and The MOG Project announced their partnership on November 13, 2019 in their shared mission to raise awareness for myelin […]
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On June 22, 2019, The Sumaira Foundation for NMO hosted its inaugural NMO Wellness Day, a day-long community event oriented to foster discussions around health and wellness as they relate to […]
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My name is Arif and I am from Jhansi, a historic city located in the northern part of India. This is my TM story… I was in my final year […]
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I was diagnosed with Neuromyelitis Optica in June of 2012 after two hospitalizations totaling 5 months, during which I lost all my strength, ability to move and all feeling from […]
Read MorePosted by: The Sumaira Foundation in Caregiver, NMO, Voices of NMO
My name is Jamie and I am Adam’s partner of 17 years. This is Adam’s NMO story from my perspective… Everything was perfect in our lives; Adam had a good […]
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I have never been a person that likes to sit still; I don’t even like going to the movies. If it was up to me, I would run from location […]
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We are hosting our first black-tie event, NMO Awareness Gala at the beautiful Liberty Hotel Ballroom. Please join us for an evening filled with delicious food and beverages, DJ and dancing, […]
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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
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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