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Every person comes into this world with their own charm and individuality. Some babies arrive with a fiery spirit, while others are naturally calm—but one thing is certain: no two people are the same.
One of humanity’s greatest strengths lies in our shared foundation and in the way we’ve learned, over time, to value and embrace our differences.
Nicole Hall sometimes worries about the future of her daughter, Winry, who was born with a very distinct appearance. Nicole has dedicated herself to spreading knowledge about a rare condition known as congenital melanocytic nevi (CMN).
What is CMN?
CMN refers to birthmarks or moles that appear at birth or shortly after. They are fairly common and usually harmless, though in some cases they may present medical risks. Treatment is not always necessary, but doctors may recommend removal for health or cosmetic reasons—most often to reduce the chance of skin cancer.
When Winry first came into the world, doctors initially thought the mark on her face was a bruise. Soon after, they realized it was congenital melanocytic nevi.
“When they placed her in my arms, I assumed it was just a bruise. But quickly it became clear it wasn’t. To me, it looked very similar to a mole,” Nicole told Good Morning America.
Specialists like Dr. Harper Price from Phoenix Children’s Hospital and Dr. Heather Etchevers from Marseille Medical Genetics explain that CMN can cause patches of darker pigmentation to appear across the body.
Although the chances are low, large birthmarks like Winry’s can slightly increase the risk of developing melanoma, a form of skin cancer. For that reason, Nicole is careful—Winry always wears sunscreen and hats when outdoors, and regular checkups with a dermatologist are a must.
“Her happiness and health come first. Sunscreen, hats, and monitoring are part of our routine. I know our dermatology visits will be very important as she grows,” Nicole says.
Still, Nicole and her husband are prepared for another challenge: the reactions of others. They know some people may stare, whisper, or even be unkind. This is why Nicole actively works to educate others and normalize her daughter’s condition.
“For many people, this is their very first time seeing a birthmark like Winry’s. Sharing our story helps spark conversations among parents and children about differences. It also helps families who have kids with birthmarks feel represented and less alone,” she explains.
Despite everything, Winry is a bright, joyful child.
“She beams with happiness. She’s almost always giggling, squealing, and chatting away. She’s full of life and already has a little sass to her—I can tell she’s going to keep us on our toes,” Nicole laughs.
Through platforms like TikTok, Nicole has connected with other families of children living with CMN. Together, they are building a supportive community and showing the world that no one is ever truly alone.
