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Every gift builds strength, safety, and connection for families facing CMN

Together We’re Climbing Toward $75,000
One Family, One Story, One Act of Hope at a Time.

Every dollar strengthens the treehouse and the families it holds.

$0

Help build a Treehouse of hope

Tough like

Teddy

When Teddy was Born, the Delivery Room Went Quiet.

The nurses said the markings on his skin were just bruises from the

C-section. A doctor told his parents, Jessica and Danny, that it was “just cosmetic.” They were discharged with reassurances but no real answers.

They brought their newborn son home, and carried fear with them.

They searched for explanations, but found little comfort. A pediatric dermatologist offered outdated information. Online searches led to frightening dead ends. They felt lost, as if they were wandering through a dense forest with no map, no light, and no one to call out to.

Until they found Nevus Outreach.

For the first time, someone understood what they were going through. Other parents had stood where they were standing. There was knowledge here, credible knowledge. And something more: connection. Support. The beginnings of hope.

And soon, they would need all of it.

One spring afternoon, Teddy came in from playing outside. Jessica noticed a spot on his nevus that looked darker than usual. It faded, but her instincts told her something wasn’t right.

 

Danny had seen it, too.

 

They pushed for a biopsy. And then came the waiting.
 

"Those three weeks felt like three years," 
  -Jessica

And then the phone rang. 

 

Melanoma.

 

One word. And in an instant, their world cracked open.

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Drawing. Laughing. Beating his brother at Mario Kart. Telling stories. Dreaming about what he wanted to build when he grew up.

He had a favorite project: a treehouse.

He drew it again and again...each time adding more detail. A climbing ladder. A lookout window. A rope swing. A snack shelf. A secret password.

 

A space big enough for his brother. Strong enough to feel safe.

 

To Teddy, it was more than a playhouse.
 

But Teddy Was Still Just Teddy

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That’s what your gift builds… something solid for families like Teddy’s.

$60

Provides newly diagnosed families with trusted medical information, so they don’t have to search alone.

$250

Connects parents with others who understand exactly what they’re facing and brings comfort no medical book can.

$500

Supports our patient registry, helping researchers and families see what’s ahead—and how to prepare for it.

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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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