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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 […]
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Posted 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 […]
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Posted 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
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Posted by:
The Sumaira Foundation
in News & Announcements
Register today! www.tinyurl.com/NMOdayNE
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Posted 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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Posted 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 […]
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Posted by:
The Sumaira Foundation
in Blog Posts
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Posted by:
The Sumaira Foundation
in NMO, ON, Patient, TM, Voices of NMO
Meet Dionne, a vibrant 46-year old, former nurse, mother of 2 from New Orleans, Louisiana who has been living with NMO since 2009. Click below to watch Dionne share her […]
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Posted by:
The Sumaira Foundation
in NMO, ON, Patient, TM, Voices of NMO
Meet Megan, a 16 year old NMO patient who and YouTube sensation (@PerfectlyKnitBeauty) who has been coping with her chronic illness through the use of makeup. We laud her courage, […]
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Posted by:
The Sumaira Foundation
in NMO, Patient, TM, Voices of NMO
She thought she had a bad sunburn… Lillian had gone camping with her daughter and her Girl Scout troop in September of 2015. When she returned home, her shoulders and […]
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