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Posted 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 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 […]
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 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Thank you to our fabulous guests, featured speakers Drs. Dean Cestari and Marcelo Matiello, Chef Bouley + the Bouley Culinary Team for helping us raise NMO awareness us at The […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
In October 2015, as I was traveling to Oklahoma to visit my sister, I developed a deep gray-teardrop-shaped spot in my right eye which increased after I arrived. I mentioned […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
The 3rd Annual NMO Awareness Gala SATURDAY, MARCH 24, 2018 | DOORS OPEN AT 7:00PM MANDARIN ORIENTAL, GRAND BALLROOM (BOSTON, MA) You’re invited to the first-ever Bollywood theme* black-tie gala […]
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