a rare approach

to a rare disease

The NMO Story

To learn more about this rare disease, view our entire video library for more information.

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NMOtion - Get Involved!

Learn more in how you can help make a difference with the options below.

  • Learn About
    Clinical Trials

    Learn how clinical trials work, whether or not you're eligible to participate, and the possible risks and benefits.

  • Advocate

    A disease is not rare if it affects you, so get the resources you need to join the community and get NMotion to solve NMO!

  • Give Blood

    If you know someone who has been diagnosed with NMO, please help us with blood samples and/or clinical data donations to our Biorepository.

  • Donate

    100% of all donations go straight to scientific research. Support our rare approach to a rare disease.

  • Share

    Help yourself and others by telling your story. Not only are you expressing yourself, but you are also giving an insight to others who may be seeking guidance in some way.

  • Recommended Reading

    Learn more about the larger conversation surrounding health, mindfulness, and autoimmunity with the recommended readings.


The Guthy-Jackson Charitable Foundation is dedicated to funding research to understanding the pathophysiology and biochemistry of NMO. Learn more about our sponsored institutions below.

Guthy Jackson Research
View All Current Research

Events & News Updates

From advocacy events and support groups to news articles and videos, find more ways to stay updated get involved in the NMO community.

  • NMO in the News

    Browse our Press page with articles and videos from The Washington Post, The Huffington Post, and more.

  • NMO Patient Day

    Find photos, videos, and more from the 2017 NMO Patient Day held in Los Angeles, CA.

  • Advocacy Events

    Learn more about advocacy events happening in the future or schedule your own.

NMO News.

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