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NMO STORIES AROUND THE GLOBE

Rare to the Rescue

  • In My Words | Sandra Adda

    In My Words | Sandra Adda

    For Sandra, NMO patient advocacy is not a job, or a chore, it is a way of life. Her illness has deepened both her resilience and her compassion. She loves helping others achieve their full potential.

  • Hear My Voice | Emily Woolf

    Hear My Voice | Emily Woolf

  • Hear My Voice | Tamanika Zinger

    Hear My Voice | Tamanika Zinger

  • Hear My Voice | Megan Woolf

    Hear My Voice | Megan Woolf

  • Hear My Voice | Nell Choi

    Hear My Voice | Nell Choi

  • Hear My Voice | Monica Jones

    Hear My Voice | Monica Jones

  • Hear My Voice | Maggie Kang

    Hear My Voice | Maggie Kang

  • Hear My Voice | Sandra Adda

    Hear My Voice | Sandra Adda

  • Hear My Voice | Shekita Green

    Hear My Voice | Shekita Green

  • Hear My Voice | Heather Sowalla

    Hear My Voice | Heather Sowalla

  • Hear My Voice | Kristin Wiedower

    Hear My Voice | Kristin Wiedower

  • Mysterious and challenging life experience. Living with NMSOD

    My journey began with a non definitive diagnosed illness, I have learned NMSOD mimics other illnesses from lupus to MS. I stayed at many hospitals with the Hope I would be cured. Had tried all types of medications, from morphine to calm me (mind though at ER everyone thought I lost my mind due to…

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NMO Stories exists to provide everyone with a voice, every stakeholder for NMO from patients and caregivers to clinicians and nurses.

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