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More Than a Denver Meetup: Finding Connection in the Nevus Community

The recent Nevus Outreach rally in Denver radiated warmth, connection, and a powerful sense of community. For many families, including first-time attendees, the event offered a unique opportunity to connect in person with others who share similar experiences. With three nevus owners present—including a 6-week-old—and two sets of grandparents, the gathering highlighted the diversity and strength within the community. Hosted at a local restaurant, the setting allowed for relaxed, meaningful conversations, creating a space where attendees could share stories, offer support, and simply enjoy one another’s company.


Three people smiling, posing together indoors. One wears a patterned shirt, another a brown sweater, and the third a shirt with rainbow design.

What made this rally especially impactful was its emphasis on informal connection over formal programming. Unlike larger conferences, this more intimate event centered on conversation, support, and shared experience. Attendees found comfort in realizing they are not alone—whether as parents navigating medical decisions or as individuals living with nevi. One family shared how their motivation to attend stemmed from a desire to build a local community after experiencing the powerful support of last summer’s national conference. These personal stories reminded everyone that even though congenital nevi are rare, the journey doesn’t have to be a lonely one.


Looking ahead
Two women smiling in a car. Both wear badges with a child’s photo. One wears a gray hoodie, the other a white sweater. Warm, friendly mood.

The momentum from this rally is already sparking future plans, including hopes for another meetup this summer in the Denver area. “The biggest thing is showing up, the physical presence we have for each other is one of the most valuable forms of support that we can provide.” says host Sarah Nelson-Taylor. It’s a reminder that while research and resources are critical, sometimes the most meaningful support comes from being physically present, sharing a meal, and saying, "We’re in this together”.




A group of adults and children pose happily in a plant-filled indoor setting. Casual attire and colorful outfits create a cheerful atmosphere.


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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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