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Posted by: The Sumaira Foundation in News & Announcements
We are proud to announce the launch of TSF Spark Grants! Frequently Asked Questions Who is eligible for the grant award? Clinical, translational and basic researchers with experience in […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Here is my story of how I was diagnosed with Neuromyelitis Optica and just how scary it can be knowing that something is wrong but not being able to find […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
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Read MorePosted by: 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, […]
Read MorePosted by: 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. […]
Read MorePosted by: 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 […]
Read MorePosted by: 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 […]
Read MorePosted by: 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 […]
Read MorePosted 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 […]
Read MorePosted by: The Sumaira Foundation in MOG, Patient, Voices of NMO
Liz has had NMO for 25 years now. She’s only known it for ten… Since she’d had migraines throughout her childhood, Liz and her mother didn’t think too much […]
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