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Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
This disease began with hiccups and vomiting 25+ times a day. I was certain that I had gotten food poisoning or had the flu. Later, I learned that things would […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Sumaira’s NMO Story From the Transverse Myelitis Association blog, In Their Own Words (October 4, 2018) My name is Sumaira and I am the founder and executive director of The Sumaira Foundation […]
Read MorePosted by: 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 […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
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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 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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Thank you to everyone who made the 2nd New England NMO Patient Day a spectacular day! Special thanks to: Brigham and Women’s Hospital Massachusetts General Hospital The Guthy-Jackson Charitable Foundation […]
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Register today! www.tinyurl.com/NMOdayNE
Read MorePosted by: The Sumaira Foundation in Patient, TM, Voices of NMO
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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