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Posted by: The Sumaira Foundation in News & Announcements
We launched our quarterly newsletter on Earth Day 2017! Subscribe to our quarterly newsletter by clicking the subscribe button or CLICK HERE If you have comments, suggestions, or would like to […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
On a warm February evening at the University of Miami, I sat in my Music Business lecture and wondered from where this strange soreness had come. There was a lingering […]
Read MorePosted by: The Sumaira Foundation in MOG, NMO, Professional, Voices of NMO
I was an on-call intern late one night at the Johns Hopkins Hospital when I met a young woman who presented with weakness and pain in her legs. This was […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Published on Socially Superlative‘s website. Written by Jenicka Hornung On Saturday, March 25th 2017, decked out in black tie roaring 20s attire, philanthropists gathered at the Mandarin Oriental Hotel in Boston […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
February 1st, 2011 – I began having vision problems in my left eye and a few days later, it got drastically worse. I went to the Mass Eye and Ear Infirmary’s […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Join us in black-tie attire for a roaring 20’s affair! The 2nd Annual NMO Awareness Gala Saturday, March 25, 2017 Mandarin Oriental, Grand Ballroom for the benefit of: The Sumaira […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Since she already had been diagnosed with lupus, Raynaud syndrome, and Sjogren’s syndrome, Adria didn’t think much about the tingling in her hands that started in February of 2016. Besides, […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
I was diagnosed with Neuromyelitis Optica Spectrum Disorder (NMOSD) in November 2013. My symptoms started June of that year with my toes going numb, shortly after returning from a cruise […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
My name is Ashlee. Thank you for taking the time to read my story. I’m not really sure where to begin and I’ve never publicly shared my NMO story before […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
On March 5, 2016, The Sumaira Foundation hosted its 1st Annual NMO Awareness Gala at The Liberty Hotel Ballroom. We’re proud to declare this event as a huge success and share […]
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