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Posted by: The Sumaira Foundation in News & Announcements
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 […]
Read MorePosted by: The Sumaira Foundation in NMO, ON, Patient, Voices of NMO
Ann and her husband were at the seaside, collecting seaweed to use in a kitchen garden they were digging. Ann noticed a tightness in and around her chest, but assumed […]
Read MorePosted by: The Sumaira Foundation in NMO, ON, Patient, TM, Voices of NMO
My name is Jeanette McCourt from Arizona and I was diagnosed with Neuromyelitis Optica on June 1, 2016. This diagnosis did not come easily or quickly. I had multiple diagnoses […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
Find your legislators here: https://whoismyrepresentative.com If you have additional questions or need help, please contact Gabriela
Read MorePosted by: The Sumaira Foundation in News & Announcements
Register today! www.tinyurl.com/NMOdayNE
Read MorePosted by: The Sumaira Foundation in News & Announcements
Thank you to everyone who made our NMO picnic in the Park such a wonderful day! We loved kicking off autumn at the Parkman Bandstand in Boston Common, especially alongside our NMO superheroes, families, friends + and the […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
Recently, Ria’s mother’s blood pressure climbed dangerously high. Her father is scheduled for a triple bypass later this week. It’s been an unusual few months for a woman who has […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, TM, Voices of NMO
I was diagnosed with Neuromyelitis Optica in June of 2012 after two hospitalizations totaling 5 months, during which I lost all my strength, ability to move and all feeling from […]
Read MorePosted by: The Sumaira Foundation in NMO, Patient, Voices of NMO
The Diagnosis My NMO journey started after my 29th birthday in January 2016. I had a headache that would not go away. It was unlike anything I had experienced before. […]
Read MorePosted by: The Sumaira Foundation in News & Announcements
We’re celebrating our NMO superheroes as we kick off the school year this autumn! This will mark our 1st community event for children, teens, and young adults with NMO patients […]
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