Since the day we were born, each of us has been distinct and wonderful. Some children have a temper from birth, while others are more peaceful, but everyone has a different outlook.
One of the most amazing aspects of being human is that we are all built the same, and we’ve evolved to the point where we can embrace and enjoy our diversity.
Nicole Hall is concerned that her gorgeous daughter Winry may have difficulties as she grows up due to her unusual attitude. She is passionate about raising awareness about congenital melanocytic nevi.
Congenital Melanocytic Nevi (CMN): What Is It?
Congenital melanocytic nevi are moles that appear at birth or develop within the first few months of life (CMN).
They are fairly frequent and, in most situations, do not pose any health risks. They do, however, pose hazards. Most cases of CMN do not require treatment, however in some circumstances, the moles may be removed. This is typically done to reduce the risk of skin cancer or to improve one’s appearance…
The world will be a wonderful place as long as we accept our differences. We welcome division in coexistence if we divide as a species because of our differences.
Winry stood out from the other newborns when she was born. They initially thought it was a bruise, but subsequently learned it was a congenital melanocytic nevus.
“When they originally delivered her to me, I mistook her for a bruise. My spouse and I realized right away that it wasn’t a bruise. “And, as the name suggests, I thought it looked like a mole,” mom Nicole Hall told Good Morning America.
According to Dr. Harper Price of Phoenix Children’s Hospital and Dr. Heather Etchevers of Marseille Medical Genetics, her disease causes black and brown patches to form on various portions of her body.
One mother is determined to show her daughter that she is more than gorgeous.
As previously said, like other moles, especially one of that size on her face, she is at danger of acquiring melanoma, a type of skin cancer. Although the risk is modest, Nicole always wears a hat when they are outside in the sun. She also applies sunscreen to Winry and takes all precautions.
“Our first priority is her health and happiness. We’ll have to keep an eye on her with sunscreen. I’m careful with caps and other accessories. “I’m sure our regular dermatological appointment will be our closest buddy as we grow older,” Nicole says.
“When they originally delivered her to me, I mistook her for a bruise. My spouse and I realized right away that it wasn’t a bruise. “And, as the name suggests, I thought it looked like a mole,” mom Nicole Hall told Good Morning America.
According to Dr. Harper Price of Phoenix Children’s Hospital and Dr. Heather Etchevers of Marseille Medical Genetics, her disease causes black and brown patches to form on various portions of her body.
One mother is determined to show her daughter that she is more than gorgeous.
As previously said, like other moles, especially one of that size on her face, she is at danger of acquiring melanoma, a type of skin cancer. Although the risk is modest, Nicole always wears a hat when they are outside in the sun. She also applies sunscreen to Winry and takes all precautions.
“Our first priority is her health and happiness. We’ll have to keep an eye on her with sunscreen. I’m careful with caps and other accessories. “I’m sure our regular dermatological appointment will be our closest buddy as we grow older,” Nicole says.
Winry’s parents are aware that there are individuals in school who will point at her, stare at her, and call her names. That is why they are committed to raising awareness about her disease.
“For many individuals, this is their first time seeing a birthmark like hers, which is why I enjoy sharing,” Nicole explains. “This is an excellent dialogue for parents to have with their children to see how children differ, or for parents who have a child that looks like Winry or has any kind of birthmark to see how their child is portrayed.”
Winry is a happy and healthy child, and her parents hope that she embraces her appearance while she is young so that she will be able to manage later in life.
“She just exudes happiness. She’s either laughing or shrieking all the time. “She is the happiest baby I have ever seen,” the mother said. “She’s already a huge talker. We haven’t said anything yet, but she tells it like it is and she’s already gaining a little sassiness, so I think we’re going to have a lot on our hands.”
Nicole is raising awareness about her daughter’s condition on social media, particularly TikTok, and parents with children with CMN are already supporting the cause.
They are aware that they are not alone.
