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Share Your Rare

At Nevus Outreach, we believe that every story makes a difference—especially yours. Sharing your experience with congenital melanocytic nevi (CMN) helps others feel seen and reminds them they’re not alone. Your voice has the power to spark hope, build understanding, and inspire meaningful change for those on a similar path.

Host an Event. Inspire Connection. Create Change.

Bring your community together for awareness, connection, and hope—whether it’s a Rally for Rare, a Nevus Neighbors gathering, or a gala that lights the way for progress. 
 

From neighborhood meetups to large-scale galas, every event you host helps shine a light on CMN and NCM—and strengthens the community that makes Nevus Outreach so special. Or

Host an event that connects hearts, builds awareness, and fuels the mission—one neighbor, one story, one night at a time.

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Your Story Has Power

By opening up and sharing your rare story, you become a powerful advocate for awareness and change. Whether it's a heartfelt message, a meaningful photo, or a short video, your contribution helps educate others, encourage families on similar journeys, and strengthen the CMN community. Every story shared brings us one step closer to greater understanding, increased support, and continued progress in research and resources.

Ready to share?

Send us your favorite photos, videos, or written stories. With your permission, they may be used to support advocacy, fundraising, and public awareness efforts through Nevus Outreach.

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Get in touch:

Phone:  501-500-1932

Email: info@nevus.org

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Address:

361 Southwest Drive, #353

Jonesboro, AR 72404

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Join Our Team!

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Being a part of the community can help nevus owners know that they're not alone. None of us are alone.
Our Mission:

Nevus Outreach is dedicated to driving awareness, fostering a supportive community, and advancing research for people affected by congenital melanocytic nevi and related conditions.

EIN: 59-3455128

Nevus Outreach is a registered 501(c)(3) nonprofit organization dedicated to supporting individuals and families affected by CMN and NCM.

Medical Disclaimer: The information provided on this website is for educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider regarding medical concerns.

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