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Blue dots that are part of Nevus Outreach's branding

We have a mission.

Awareness, Support, Research.

Little Girl with Giant Nevus
We are so glad you found us.

Welcome to the nevus family!

Whether you are a nevus owner, a new parent of a child with a nevus, or someone who just wants to know more about congenital melanocytic nevi, we're here to help.

We have been in your shoes.

The co-founders of Nevus Outreach, Inc. created this organization to help new parents of children with large nevi. They know firsthand the stress that misinformation can create, as one of the co-founders was told that his daughter's condition was terminal when she was born. Over two decades later, his daughter is healthy and happy. Unfortunately, many new parents of children with large nevi are told the same frightening misinformation. Nevus Outreach, Inc. provides support and information to help parents make informed decisions about their child's care.

A young girl with nevus smiles while being held by her dad

If you are the parent of a baby who was born with a large mole or a large birthmark, it is very possible that your child was born with a nevus and you have come to the right place! We are here to give you the answers and the support you need.

A family of 3 holds signs that share information about how they are raising awareness about CMN and NCM

We're here to help.

Frequently Asked Questions

Here are the answers to the questions we get asked the most about congenital melanocytic nevi (also referred to as CMN). Our goal is to provide you with the information you need about large/giant congenital melanocytic nevi. 

CMN FAQs

Large congenital nevi occur approximately once in every 20,000 births.

Nevus-skin can range from thick with a folded appearance, to thin and fragile. Fragile skin can tend to tear more easily and may take a longer time healing.

Congenital melanocytic nevi form in the womb very early in development, within the first twelve weeks of pregnancy.

Nothing you did caused your child to be born with a nevus. It is not your fault.

Get in touch:

Phone:  501-500-1932

Email: info@nevus.org

Address:

361 Southwest Drive, #353

Jonesboro, AR 72404

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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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