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The Sumaira Foundation
in News & Announcements
On September 21, 2018, TSF hosted a dinner for NMO specialists + champions in Boston, MA. We engaged in great conversation about: the ongoing development of the disease ideas for […]
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The Sumaira Foundation
in News & Announcements
http://gladysmagazine.com/subscribe/bellagladys
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The Sumaira Foundation
in MOG, NMO, Professional, Voices of NMO
My name is Tracey Cho. I am a neurologist and a teacher. I specialize in autoimmune and infectious neurology, treating diseases like NMO, NMDA receptor encephalitis, HSV encephalitis, chronic meningitis, […]
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The Sumaira Foundation
in NMO, Patient, TM, Voices of NMO
Paula is a walking miracle. She looks good, feels good and can do most everything she ever did in her life, though she is now eligible for senior discounts. […]
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The Sumaira Foundation
in NMO, Patient, Voices of NMO
Meet the happy workaholic, Kelly Ann, an ambitious business + LinkedIn coach, podcaster and luxury brand consultant from California who candidly shares the ups and downs of her NMO story […]
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The Sumaira Foundation
in News & Announcements
NEWS FLASH! The 3rd NMO Awareness Gala is featured in the latest edition of Improper Bostonian Magazine’s “Proper Bostonians” section! Thank you Dana Bisbee and friends at Improper Bostonian for helping us illuminate […]
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The Sumaira Foundation
in News & Announcements
Support The Sumaira Foundation with every swipe! We’re excited to announce our partnership with Charity Charge, the MasterCard that contributes a 1% cash back donation to our nonprofit every time […]
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The Sumaira Foundation
in NMO, ON, Patient, TM, Voices of NMO
Julie has had NMO for at least a dozen years. From before and since that time, she has been diagnosed with a number of other conditions. She has been […]
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Posted by:
The Sumaira Foundation
in News & Announcements
On March 24, 2018, The Sumaira Foundation for NMO hosted its 3rd Annual NMO Awareness Gala at the Mandarin Oriental, Boston. 3 WAYS YOU HELPED US ILLUMINATE THE DARKNESS OF […]
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Posted 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 […]
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