Every single one of us has something unique and lovely inside of us from the moment we are born. While some kids are calmer than others, some people have tempers from birth. But every person sees things differently.
One of the best things about being human is that we all have the same physical characteristics and that, for the most part, we have learned to value and embrace our differences.
Nicole Hall is concerned that Winry may face challenges in life as she ages as a result of her unique outlook. Congenital melanocytic nevi are a condition she wants to make more people aware of.
What Is Congenital Melanocytic Nevi (CMN)?
Moles that are present from birth or that appear within the first few months after birth are known as congenital melanocytic nevi.
They are fairly common and usually do not have a negative impact on health. However, they could pose risks. Although the majority of CMN cases never require treatment, in some cases the moles may need to be removed. Usually, this is done to improve appearance or lower the risk of skin cancer.
If we can coexist in harmony with one another’s differences, the world will be a wonderful place. We seek division if our differences cause us to split up as a species.
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.
I initially thought it was a bruise when they brought her to me. It wasn’t a bruise at that point, my husband and I quickly realized. The mother, Nicole Hall, stated, “It reminded me a lot of a mole. “.
Harper Price of Phoenix Children’s Hospital and Heather Etchevers of Marseille Medical Genetics conducted a study on her, and it revealed that she has a disease that causes numerous black and brown patches to appear all over her body.
As we previously mentioned, there is a possibility 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, even though the risk is small. She also gives Winry sunscreen and takes all necessary precautions.
“She is our most important concern.
Sun protection is necessary for her.
When wearing hats and similar accessories, I exercise extra caution. We’ll definitely grow up to think of our regular dermatology appointments as our best friends, Nicole continues.
Winry’s parents are aware that she will meet rude classmates who will glare, yell, and point at her. As a result, they are dedicated to helping spread information about her illness.
One of the reasons Nicole enjoys talking about her birthmark is that many people are seeing them 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 parents who do have a kid that looks like Winry or has any kind of birthmark to have their child represented.”.
For Winry to be able to deal with her appearance later in life, her parents hope she embraces it while she is still young. She is a young girl in excellent health and happiness.
Simply put, she exudes joy.
Her screams and laughter essentially never stop. The mother said, “She’s the happiest baby I’ve ever seen.”.
Nicole is using social media, especially TikTok, to spread awareness of her daughter’s condition, and parents of kids with CMN have already joined in.
They realize they’re not by themselves.
