Welcome to the Community
Mike found Nevus Outreach in October 2016 at age 55, and says it was life changing to see and meet others with nevus. He was one of the first to become an official member with the organization, and even assisted in the beta-testing process. Thanks, Mike!
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.
Register to view this stunning gallery featuring 30 portraits of adults and children with CMN. Learn More »
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.
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.
Nevus Outreach is dedicated to bringing awareness, providing support, and finding 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.