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Vaish and her spouse Jacob have two boys: Ezra and Gabriel. Their family lives in Malaysia and they travel often to the United States for Ezra's treatments. We had the pleasure of meeting them at the REUNITE 2022 conference in Denver!
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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.
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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.
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
Nevus Outreach is dedicated to bringing awareness, providing support, and finding cures for people affected by congenital melanocytic nevi and related disorders.
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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.
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