Meet the New Nevus Outreach - Brand Identity

Meet the New Nevus Outreach - Brand Identity

We are excited to envision the organization's growth and progress in the next 25 years and beyond. In the next few months, we will be launching a brand new website at

See our branding Story here. »

Member Spotlight

Member Spotlight

Stephanie and nevus owner daughter Hannah Delaney live in Petaluma, California. Their family has been connected to Nevus Outreach since its inception in 1997, and are now official members as part of the membership program!

Become a member to receive full member spotlight stories! »

Welcome to the nevus family.

Welcome to the nevus family.

In the next few months, we will be launching a brand new website at and other elements that align with this fresh look for the Nevus community.

Hear our Branding Story here. »

Become a Member of Nevus Outreach

Become a Member of Nevus Outreach

Welcome to the Community!

Read More & Register »

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

Virtual Gallery Opening Soon!!!! How do you C Me Now!

Register to view this stunning gallery featuring 30 portraits of adults and children with CMN. Learn More »

Announcing Membership!

We are excited to welcome every single individual to Nevus Outreach and are so glad to have you as a part of this growing community. We look forward to connecting with you! Learn More »


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 »


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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