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We’re Gearing Up for Summer Campfire Chats

A navy banner is featured on the top of the page with the words "Nevus Outreach Summer Campfire Chats" displayed. Off to the right, there is a faint image of a roaring campfire with people actively roasting marshmallows on metal skewers over the flames.

There’s something powerful about coming together—sharing stories, learning from one another, and realizing you’re not alone. That’s the spirit behind our Summer Campfire Chats, and we’re so excited to bring this series to life for our community.


This summer, on the last Thursday of each month, we’ll gather (virtually) to connect, learn, and grow together—focusing on the topics that matter most to individuals and families impacted by CMN and related conditions.


🌿 What to Expect

Each Campfire Chat is designed to spark meaningful conversation, provide valuable insight, and strengthen the bonds that make this community so special.

Here’s what we have planned:


🗓 May 28, 2026 – Connecting Our Community: The Conference Experience

Join Lauren Isbell, Kim, and Dannica as they share what makes the Nevus Outreach Conference such a transformative experience—and how connection plays a central role in everything we do.


🗓 June 25, 2026 – Research Roadmap (Featuring NOOR)

Hear from Danielle Bestioso and Dr. Maggie Mangold as they walk through the future of research, including updates on the Nevus Owners Outcomes Registry (NOOR) and how your participation helps drive progress.


🗓 July 30, 2026 – Strengthening Support

Ev, Marika, and Lauren will lead a conversation centered on emotional support, resources, and the ways we can continue to show up for one another.


🗓 August 27, 2026 – Moments That Matter

Kimi and Lauren will close out the series by reflecting on the meaningful moments that shape our journeys and how we can continue building a supportive, connected community.


💛 There’s a Seat for You

Whether you’re a parent, a nevus owner, a caregiver, or a supporter, you belong here. These conversations are rooted in connection, education, and the shared experiences that bring us closer together.

This isn’t just a series—it’s a space to be heard, to learn, and to feel supported.


✨ Pull Up a Seat

Bring your story. Bring your questions. Or simply come and listen. However you show up, you are part of something that matters.


📣 Stay tuned for dates, registration details, and more—we can’t wait to connect with you this summer.

A navy banner with the words "Gathering around the campfire" is above a camping tent silhouette and trees. Underneath the camping logo, there is the words "Nevus Outreach presents: Campfire Chats, A Summer Live Session". On the right half of the photo, there is a crisp image of a roaring campfire- with people actively roasting marshmallows in the flames.

Get in touch:

Phone:  501-500-1932

Email: info@nevus.org

Address:

361 Southwest Drive, #353

Jonesboro, AR 72404

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Being a part of the community can help nevus owners know that they're not alone. None of us are alone.
Our Mission:

Nevus Outreach is dedicated to driving awareness, fostering a supportive community, and advancing research for people affected by congenital melanocytic nevi and related conditions.

EIN: 59-3455128

Nevus Outreach is a registered 501(c)(3) nonprofit organization dedicated to supporting individuals and families affected by CMN and NCM.

Medical Disclaimer: The information provided on this website is for educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider regarding medical concerns.

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