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JOIN THE A-TEAM. BECOME A CMN AMBASSADOR.

AWARENESS IS EVERYTHING

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WHAT IS THE A-TEAM?

The A-Team is a community of kids and families who turn their stories into impact through fundraising. When you join and start a fundraiser, you become a CMN Ambassador—using your voice to make a difference.

HOW IT WORKS

STEP 1

JOIN THE A-TEAM

Sign up and become part of a community that truly understands your journey. The A-Team connects kids and families who want to make a difference, giving you a place where your story is seen, supported, and celebrated.

STEP 2

START YOUR FUNDRAISER

Choose a fundraiser that fits your personality—whether it’s a challenge, event, or awareness campaign. Set a goal, share your story, and invite others to be part of something meaningful.

STEP 3

BECOME A CMN AMBASSADOR

​As you fundraise, you step into the role of a CMN Ambassador—someone who raises awareness, inspires others, and helps create a world where every child feels confident and valued.

EVERY DOLLAR YOU RAISE BENEFITS THOSE AFFECTED BY CMN IN OUR COMMUNITY.

THIS ISN'T JUST ABOUT RAISING MONEY - IT'S ABOUT RAISING VOICES.

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1;500,000

are born with a giant CMN.

2-5%

of individuals with a large or giant CMN will develop a melanoma within the nevus or in the central nervous system.

0

right now there are 0 cures for CMN & NCM, but with you’re help we can change that.

FIND YOUR FUNDRAISING STYLE

Not sure where to start? Choose a style that fits you:

school & group fundraisers

basic online fundraiser

food & community events

fitness & goal-based fundraisers

awareness & advocacy fundraisers

celebrations & special occasions

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Light the Night shows the power of our community coming together. By starting your own fundraiser, you help shine that same light of awareness, hope, and support even further.”

ALYSSA HUSER

KANSAS CITY, MO

By joining the CMN A-Team, you're not just a donor—you're a trailblazer. Together, we can forge a path toward a brighter future, bringing hope and progress to those affected by CMN.

READY TO MAKE AN IMPACT?

JOIN THE A-TEAM AND START YOUR FUNDRAISER TODAY!

Get in touch:

Phone:  501-500-1932

Email: info@nevus.org

Address:

361 Southwest Drive, #353

Jonesboro, AR 72404

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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