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Hali’s NMO Story – No Disease Will Ever Wear Me Down

Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO

Hali's NMO Story - No Disease Will Ever Wear Me Down

My name is Hali and I am a 19 year old Scottish Law student living with NMOSD. — It all began in August 2021 when I developed a rash on […]

Tiffany’s NMO Story – Navigating the Navy with NMO

Posted by: The Sumaira Foundation in NMO, Voices of NMO

Tiffany's NMO Story - Navigating the Navy with NMO

Tiffany was a military brat with both of her parents serving in the Navy, so joining up herself seemed the obvious choice for her. She enlisted in 2006 and met […]

Allison’s NMO Story – Keep on Keepin’ On

Posted by: The Sumaira Foundation in NMO, Voices of NMO

My name is Allison and I am a married, busy mom of three children (17, 12 & 12 years old). My NMO journey started approximately seven years ago, when I […]

Julie’s NMO Story – Tingles & Tinkles

Posted by: The Sumaira Foundation in NMO, ON, Patient, Voices of NMO

Five years ago, my oldest daughter and I were grocery shopping when it occurred to me that the grocery store looked foggy or smokey. When I asked her if she […]

Pam’s NMO Story – How NMO Reinforced Positivity

Posted by: The Sumaira Foundation in NMO, Patient, Voices of NMO

On Monday morning, Pam had a headache. For a woman who never got headaches, this was notable. In addition, when she turned her eyes right and left, she experienced eye […]

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