Each of us has something unique and beautiful inside of us from the moment we are born. Some kids are irritable from birth, while others are calmer. Everyone, though, views things differently.
One of the best things about being human is that we all have the same physical characteristics and that we have mostly learned to value and embrace our diversity.
Nicole Hall worries that Winry’s unique outlook could make life challenging for her as she ages. Her goal is to increase knowledge of congenital melanocytic nevi.
What Is Congenital Melanocytic Nevi (CMN) and How Does It Occur?
Congenital melanocytic nevi are moles that either develop within the first few months of life or are present from birth.
They are fairly common and typically have no negative effects on health. However, there may be risks involved. However, the majority of CMN cases never require treatment, and in some cases, the moles may need to be removed. The usual reasons for doing this are to improve appearance or lower the risk of skin cancer.
As long as we can coexist peacefully with each other’s differences, the world will be a wonderful place. We seek division if our differences as a species cause us to split apart.
At her birth, Winry stood out from the other infants. They initially thought it was a bruise, but later realized it was a congenital melanocytic nevus.
“When they first brought her to me, I thought it was a bruise. It wasn’t a bruise at that point, my husband and I quickly realized. The mother, Nicole Hall, said, “I thought it looked a lot like a mole. “.
She has a disease that causes numerous black and brown patches on her body, according to research by doctors Harper Price of Phoenix Children’s Hospital and Heather Etchevers of Marseille Medical Genetics.
As we have already stated, there is a chance that any mole, especially one that size on her face, could develop into melanoma, a form of skin cancer. Nicole always makes sure to wear a hat when they are outside, despite the slight risk. She also gives Winry sunscreen and takes all necessary precautions.
Her welfare is our top priority, I said. The sun must be kept off of her. When wearing hats and other similar items, I take extra precautions. Without a doubt, when we’re older, we’ll look back on our regular dermatology visits as our closest friends,” Nicole continues.
Winry’s parents are aware that she will meet rude classmates who will glare, yell, and point at her. They are determined to contribute to the dissemination of information about her illness as a result.
One of the factors Nicole enjoys sharing is that many people are seeing birthmarks similar to hers for the first time. The parents of Winry said, “This is a good topic for parents with their kids to see kids have differences, or for those who do have a kid that looks like Winry or has any kind of birthmark to have their child represented.”.
In order for Winry to be able to deal with her appearance later in life, her parents hope she embraces her appearance while she is still a young girl. She is a young girl in excellent health and happiness.
She’s just happy all the time. She practically never stops yelling or laughing. The mother said, “She’s the happiest baby I’ve ever seen.”.
Parents of children with CMN have already gotten involved as Nicole uses social media, particularly TikTok, to spread awareness of her daughter’s condition.
They are conscious of their comradeship.
Please share this excellent article to increase awareness of CMN.
