NMO Advocacy Network
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Act Locally to Cure NMO Globally
The NMO Advocacy Network works with established NMO/MS Organizations throughout the world.
To download all of the items in the NMO Speaker’s Kit please click here (.zip file) or download them individually on the NMO Speaker’s Kit page.
How I Can Support the Network |
Other NMO Organizations |
Patient Stories |
View programs, event ideas and ways to support the growing NMO Advocacy Network. |
Information about other NMO Organizations such as Sistamoon, NMO Diaries and more. |
Share your story about NMO or read stories of other patients who have dealt with NMO. |
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Who is a Network Member?
- » Patients, Caregivers, Friends, Family and Community.
- » Organizations, Research and Medical Professionals.
- » Any member of the general public who raises awareness or works to find a cure for NMO.
Why is the Network Needed?
To raise awareness and leverage existing human and financial resources to reach our goal.
What Are Some Examples of an Advocate’s Role?
- » Coordinate Fundraisers, Events and Meetings in your area.
- » Work and participate with established NMO/MS organizations.
- » Raise public awareness of NMO.
