Every one of us is unique and beautiful from the moment we are born. Some children have a temper from birth, while others are more calm, but outwardly, everyone is different.
One of the most wonderful aspects of being human is that while we are built the same way, we have evolved to a point where we accept and celebrate our differences.
Nicole Hall worries that her lovely daughter Winry might face challenges as she grows up due to her unique appearance. Nicole is committed to raising awareness about congenital melanocytic nevi.
What Is Congenital Melanocytic Nevi (CMN)?
Moles present from birth, or those that develop within the first few months after birth, are known as congenital melanocytic nevi (CMN).
They are relatively common and, in most instances, they do not cause health issues. However, they can carry risks. Most CMN cases do not require treatment, but in some instances, moles may be removed to reduce the risk of skin cancer or to improve appearance.
As long as we accept our differences, the world will be a wonderful place. If we allow our differences to divide us, we invite separation in our coexistence.
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When Winry was born, she was different from the other babies. Initially, they thought it was a bruise, but they later received the diagnosis: congenital melanocytic nevi.
“When they first handed her to me, I thought it was a bruise. It quickly became apparent to my husband and me that it was not a bruise. And like the name suggests, I thought it looked a lot like a mole,” Nicole Hall told Good Morning America.
Dr. Harper Price from Phoenix Children’s Hospital and Dr. Heather Etchevers from Marseille Medical Genetics reported that her condition causes black and brown patches to appear on various parts of her body.
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As mentioned earlier, like all moles, especially one of that size on her face, there is a risk of developing melanoma, a type of skin cancer. Although the risk is relatively low, Nicole always ensures Winry’s head is covered when they are outside and applies sunscreen to her daughter, taking every precaution.
“Her health and happiness are our top priority. We monitor her with sunscreen and I’m careful with hats and similar items. Our regular dermatology appointments will likely be very important as she grows up,” Nicole says.
Winry’s parents are aware that there are unkind people who might stare, point, or say hurtful things at school. This motivates them to raise awareness about her condition.
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“For many people, this is the first time seeing a birthmark like hers, and that’s part of why I enjoy sharing,” Nicole explains. “This is a good opportunity for parents to talk to their children about differences, or for parents of kids with similar birthmarks to see their child represented.”
Winry is a very positive and healthy child, and her parents hope that she embraces her appearance while she’s young so she can cope better later in life.
“She just radiates joy. She’s almost always laughing or shrieking. She is just the happiest baby I have ever seen,” Nicole shares. “She’s already a big talker. We haven’t gotten a lot of words out, but she expresses herself clearly and is already showing some sassiness, so I think we’re going to have a lot on our hands.”
Through social media, especially TikTok, Nicole is spreading awareness about her daughter’s condition, and parents of children with CMN are already joining the cause.
They know they are not alone.
