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.
The 2018 conference will be our 11th conference, and registration is now open. Early Bird prices are from Feb 1 - Feb 28. Learn More »
The 2018 Conference early bird registration is now open! Learn More »
2018 Conference details, including dates, registration, and daily schedule information. Learn More »
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.
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.Toll-free Lifeline Support Groups Nevus Gathering
Nevus Outreach is dedicated to bringing awareness, providing support, and working toward cures for people affected by congenital melanocytic nevi and related disorders.
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.