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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.
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.
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.
