top of page

Men & CMN: The Way We Carry It- Nevus Owner, Khalid Bethea's Story


A photo collage in black and white print depicts a baby boy with CMN on his lower half. This is referred to as "Trunk nevus". It extends from mid back, down to his bottom and thighs. He has 1000s of smaller nevi, speckled on his upper back, legs, arms and face.

For as long as he can remember, Khalid Bethea has lived with Congenital Melanocytic Nevi (CMN). Born with CMN covering much of his body, his journey has been shaped by surgeries, insecurity, resilience, and ultimately, self-acceptance.

Growing up with a visible condition was not easy. As an infant, Khalid underwent surgeries to remove one of his larger birthmarks because doctors feared it could become cancerous. But for him, some of the deepest scars were emotional rather than physical.

“As a child it was tough on me mentally & physically.”

He remembers constantly wondering what others thought when they looked at him. Sometimes, those fears were reinforced in painful ways.

“Having people purposely not touch you can definitely have an effect on you as a child who is very insecure about the way you look.”

Carrying Insecurity into Adulthood


Even as he got older, those insecurities did not simply disappear. Khalid shared that one of the hardest parts of living with CMN has been learning how to feel comfortable in everyday spaces.

“I always think someone is staring or judging & I want to just crawl in a hole & hide every single time.”
A woman holds her little boy in her loving arms. He has on a hooded 90s style rain jacket. She looks down and admires him, adorning a smile across her face. The baby is looking at the camera with a toothless smile. His brown eyes looking happily at the camera with wonder. He has several small CMN speckled across his face.

For many people with visible differences, that feeling can become exhausting... constantly entering rooms already aware of how different you may appear from everyone else around you.

Khalid says he still feels different today, especially now that he also lives with vitiligo alongside CMN. But over time, his perspective has slowly changed.

“I understand not many people look like me… but I can't & don’t want to change it so I navigate it by living life normally knowing I’m ultimately a good person.”

Finding Confidence Through Connection



A young man smiles with a closed mouth, posing happily for the camera. It appears to be a yearbook photo. His hair is braided and his braids touch right down at his shoulders. His eyes are smiling too, giving a very proud appearance. He has several small nevi scattered across his face and neck.

While insecurity shaped much of his childhood, Khalid says family and friends played a huge role in helping him build confidence over the years.

They reminded him that he was often harder on himself than anyone else was. They kept him laughing on difficult days and encouraged him to keep showing up as himself.

Modeling also became an unexpected turning point in his journey. Opportunities to be seen, photographed, and embraced helped him slowly realize that his appearance did not diminish his value.

“The opportunities that I have had & the people who I have met have been a blessing.”

Over time, confidence stopped meaning “feeling perfect” and started meaning accepting himself exactly as he was.


Redefining Strength


For Khalid, strength no longer means hiding vulnerability or pretending difficult moments do not exist.

Instead, he defines strength in a much quieter and more honest way.

“To me strength is waking up every day and living your life genuinely.”

A young man sits on the ledge of a green brick wall. He looks off at the distance, holding himself up by his arms. His shirt displays a floral design of green, red, white and pastel yellow. He is wearing grey pants with a belt. He sits with a determined look on his face. He has vitiligo and CMN. The vitiligo is prevalent under his eyes, nostrils and mouth. His arms are adorned with several 100s of smaller nevi, as well as his face and neck. His sleeves are rolled up with his sunglasses tucked into his pants pocket.

That mindset has become central to how he navigates CMN today. Rather than allowing his appearance to define him, he focuses on the kind of person he wants to be.

He believes real strength comes from being open-minded, stepping outside your comfort zone, and allowing people to see who you truly are beneath the surface.


The Importance of Visibility and Vulnerability



A close up photo of a young man in a red baseball cap. He has gold rimmed, oval, Ray Bans glasses. Behind the glasses, his piercing brown eyes catch the sunlight. He has vitiligo which is prevalent around his eyes, tip of his nose and around his mouth and lips. He also has small CMN type nevi, speckled across his face and neck. The background is out of focus but appears to be at a outdoor public event.

As a man living with CMN, Khalid also believes conversations around emotional health and vulnerability matter deeply.

Too often, men are expected to carry insecurity silently. But Khalid believes sharing experiences openly can help others feel less alone.

“Everyone needs to help shape these conversations because you never know who will relate to your story or mindset.”

Today, he openly explains CMN to others when people ask questions. He wants people to understand that CMN is not contagious and not something to fear. More importantly, he wants others living with visible differences to know they deserve to take up space fully and confidently.


Learning to Love Yourself Fully


Looking back, Khalid wishes he could tell his younger self something simple but powerful:

“You’re beautiful inside & out, believe it with every fiber of your being!”

A man looks down, posing for the camera in a navy tshirt. The tshirt logo is halfway shown with a semi circle and the letters overlapping that say "bc". His gold framed Ray Ban oval glasses gently sit on the bridge of his nose. He has a reddish earing in his left ear. His hair & facial hair are long and curly- worn in a natural style. He has vitiligo and CMN, which is prevalent on his face. The patches give his face a unique look as they coexist on the model's face.

That message now extends beyond himself and toward others beginning their own journey with CMN.


He encourages people not to become trapped by fear of judgment or by the insecurities that visible differences can create. Instead, he hopes others learn to embrace who they are fully- not someday, but now.


Because in Khalid’s experience, healing does not come from changing how you look.


It comes from learning that your worth was never dependent on your skin in the first place.

5 Comments


Zaadia
10 hours ago

So proud of you bro!!! Ever since we were kids, I knew you were going to grow up to be an inspiration to others. Don't ever change!!! 😁🙌🏾

Like

Meta for Business
Meta for Business
18 hours ago

Khalid's story of turning pain into self-acceptance is powerful — it's the kind of real talk more men need to hear about carrying CMN with pride. I've been https://kling-motion.com

Like

Chelsea A
3 days ago

CMN and vitiligo! You’re literally a unicorn! Thank you for sharing your story. My daughter has a bathing suit nevus also. I hope that in this day in age, people are more interested in learning about CMN instead of being afraid of it. I’ve learned to love every “blemish”.

Like

Caroline
3 days ago

Tons of love to the king 👑 🤎

Like

Nmbutler
3 days ago

As Khalid’s Aunt, I couldn’t be more proud of the incredible young man he has become. His courage, strength, and confidence inspires everyone around him.


Khalid, watching you grow has been a blessing, and I hope you always know how deeply you are loved, supported, and admired.

Your story is powerful, your voice matters, and your journey is helping others find the confidence to embrace their own uniqueness. I love you beyond words and will always be one of your biggest supporters. Keep shining, Khalid—the world needs your light.

Like
Get in touch:

Phone:  501-500-1932

Email: info@nevus.org

Address:

361 Southwest Drive, #353

Jonesboro, AR 72404

Join Our Team!

  • Facebook
  • Instagram
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.

bottom of page