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ABOUT THE A-TEAM

More than a fundraiser—it’s a community, a voice, and a way to make a difference.

WHAT IS THE A-TEAM

The CMN A-Team is a community of passionate supporters who turn their ideas, talents, and events into fundraisers for Nevus Outreach. From hosting parties and cookouts to taking on athletic challenges or spreading awareness in their communities, A-Team members use what they love to raise funds and shine a light on Congenital Melanocytic Nevi (CMN) and Neurocutaneous Melanocytosis (NCM).

 

Every fundraiser, event, and shared story helps support research, provide resources for families, and build a stronger, more connected CMN community. When you join the A-Team, you’re not just fundraising — you’re helping create hope and progress for individuals and families affected by CMN and NCM.

WHAT IS A CMN AMBASSADOR?

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Becoming a CMN Ambassador with Nevus Outreach means stepping up for a cause that changes lives.

You’ll join a community of storytellers, educators, and connectors working to shine a light on congenital melanocytic nevi (CMN).

Whether you share your personal story, spread facts, host an event, or simply spark conversations, your efforts help others feel seen, understood, and supported.

When you start a fundraiser through the A-Team, you step into this role—using your voice to create real impact.

Sign up today and help make this year’s awareness efforts more powerful than ever.

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HOW IT ALL CONNECTS

JOINING THE A-TEAM IS SIMPLE AND POWERFUL

YOU JOIN THE A-TEAM

AND BECOME PART OF A SUPPORTIVE COMMUNITY

YOU START A FUNDRAISER

IN A WAY THAT FEELS AUTHENTIC TO YOU

YOU BECOME A CMN AMBASSADOR

USING YOUR VOICE TO MAKE A DIFFERENCE

IT'S ONE SIMPLE PATH WITH A MEANINGFUL IMPACT.

FOR MANY KIDS WITH CMN, THE JOURNEY CAN FEEL ISOLATING.

THE A-TEAM EXISTS TO CHANGE THAT.

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We believe every child deserves to feel confident in who they are, proud of their story, and supported by a community that understands them. By coming together, we’re not just raising funds—we’re creating connection, building confidence, and helping every child feel seen.

THE IMPACT

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.

That’s why every story shared, every fundraiser started, and every dollar raised matters. Your support can make a lasting impact as we raise awareness of congenital melanocytic nevi (CMN). Our community is growing every day, and groundbreaking scientific advances are within reach, thanks to contributions like yours.

WHAT YOU'LL GAIN

COMUNITY

A supportive community that understands your journey

TOOLS & SUPPORT

Tools and ideas to help you fundraise with confidence

A PLATFORM

A platform to share your story and inspire others

REAL IMPACT

The opportunity to make a real and lasting impact

READY TO MAKE AN IMPACT?

JOIN THE A-TEAM AND START YOUR FUNDRAISER TODAY!

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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

THE CMN
A-TEAM CHANGES LIVES.

Awareness in the Delivery Room.

Awareness of Accurate information.

Awareness of Expertise within the Care Team.

 

But most importantly, Awareness of People Like You.

People in this community who care.

Awareness that they are not alone.

Awareness that Nevus Outreach is a worthy cause to champion.

 

Awareness is Everything. Will you join our A-Team 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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