Affected by NCM? Help us apply for research funding!

Affected by NCM? Help us apply for research funding!

Nevus Outreach has the opportunity to submit an application the Chan Zuckerberg Rare as One Project in June 2021. We are choosing to narrow our focus this year and ask the foundation to significantly support research for Neurocutaneous melanosis (NCM).

Complete our NCM Survey today! »

2022 International Conference

2022 International Conference

Nevus Outreach and the Board of Directors have decided to postpone the 2021 Nevus Outreach Conference and Reunion in Colorado Springs. The new dates are confirmed for 2022; mark your calendars for July 13-15, 2022!

More Info »

Nevus Community Mourns Loss of Paul Coleman, Chair Emeritus

Nevus Community Mourns Loss of Paul Coleman, Chair Emeritus

Chair Emeritus Paul Coleman shares his heart with the Nevus Community

Click here to read Paul's full Adieu address »

Best Practices Guidelines Now Available

Best Practices Guidelines Now Available

Complied information you can share with your doctor!

More Info »

Happy mother holding her daughter who has a large congenital melanocytic nevus

Welcome to the Nevus Family

We are so glad you've found us. Whether you are a nevus owner, an new parent of a child with a nevus, or someone who just wants to know more about large congenital melanocytic nevi, we're here to help.

Learn more about large CMN »

The Latest from the Nevus Community

COVID-19 Delays Conference, Mark Your Calendar for July 13-15, 2022 in Colorado Springs, Colorado.

The Board of Directors voted to postpone International Conference due to COVID-19 uncertainties. Learn More »


Nevus Outreach announces new CEO

Lauren Isbell to serve as next Chief Executive Officer Learn More »


Testimonial

We are so thankful for Nevus Outreach and the support we've received since our daughter was born with a nevus. It's so nice to have the friendship of other parents who understand and can help us.



Baby with large congenital melanocytic nevi

New Nevus Parents

If you are the parent of a baby who was born with what looks like a large mole or a large birthmark, it is very possible that your child was born with a nevus, & you have come to the right place! We've been in your shoes, & we'll do everything we can to educate & support you & your family.

We're here to help with answers & support »


We'd Love to Get to Know You

One of the best ways that Nevus Outreach can offer support to people with nevi is to connect them with people who know first-hand what they are going through. Check out the links below to connect with other members of the nevus community.

Support Groups Nevus Gathering

Get to Know Us

Nevus Outreach is dedicated to bringing awareness, providing support, and finding cures for people affected by congenital melanocytic nevi and related disorders.

Learn more about Nevus Outreach »


Rita
Rita
James
James
Joshua
Joshua

Three little girls with nevi playing together

Nevus Removal

There are several reasons that patients sometimes decide to undergo removal of a large nevus. Most of the time, the overriding reasons to remove a congenital pigmented nevus are first to reduce melanoma risk and second to improve appearance, which can be fundamental to improving a patient's overall psychosocial state.

Learn more about removal & treatment options »


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