Nevus Outreach, Inc., The association for Large Nevi and related disorders.


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Nevus Outreach 2016 Newsletter Now Available!
Celebrate: The doctors, the conferences, the families… As Nevus Outreach approaches its 20-year anniversary, we can cite numerous milestones and achievements…all worthy of praise. I will focus on the major standouts from my perspective as a board member, mother to a child with a giant nevus, and as a “family” member of the Nevus Family. (more)

Thankful for Grassroots Support
At Nevus Outreach we know it takes a village. We know we cannot do what we do without the support of the families and friends of people who are touched by our disease. For this we are thankful. (more)

World-Wide Study
Nevus Outreach, in collaboration with Naevus Global and University Children’s Hospital Zurich, has begun a comprehensive world-wide study on the well-being of children and adolescents born with a congenital melanocytic nevus (CMN), and the well-being of their parents. Eligible for this study are parents of a child born with a nevus (from birth to 18 years old) and adolescents born with a nevus (ages 14-18 years). All cases count, whether the nevus has been surgically removed or not. The input of each family and teenager is important.
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Nevus Removal 101
Whether or not to remove a congenital melanocytic nevus (CMN) is a decision no parent wants ever to face. But when a baby is born with a large nevus, parents must decide what they believe is best for their child, who is unique and precious. (more)

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Nevus Removal with various medical instruments


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