Nicole Lucas Hall is a loving mother of two, Asher, 14, and Winry, 13 months. She’s a fighter like any other respectable parent. Nicole has an ordinary existence, but she has a goal: to appreciate her daughter’s distinct beauty. Winry was born with a rare birthmark that covers one-quarter of her face at 13 months old.
Nicole recalled the first time they saw their daughter, saying that their first thoughts were perplexity and worry for her safety because neither of them had seen anything like it before.
Winry was born with rare congenital melanocytic nevi, also known as CMN, which has a 1 in 50,000 chance of occurring. They believed it was harmful because of its appearance, but the doctors quickly quieted their worries. Winry was born with uncommon congenital melanocytic nevi (CMN), which has a prevalence of about 1 in 50,000 births. They were reassured that the birthmark is most likely only cosmetical and that any health issues would be comparable to other nevi or moles.
When Winry was born, Nicole and her spouse were ecstatic. They could finally relax and enjoy Winry’s arrival even more after a long breath of relief. Her parents’ main objective today, months after her birth, is to keep their daughter healthy and positive about herself.
Unfortunately, since Nicole began sharing her daughter’s story, there has been no dearth of hostile remarks and criticism, but even in their day-to-day life, some people give Winry unfavorable gazes.
Nicole, on the other hand, has been rather laidback about it. She informed us that they both preferred to keep most of their social media comments informative because almost all of the bad feedback they received was due to ignorance. Nicole and her husband respond to people who are obnoxious and spiteful with humor.
They’ve also been largely overwhelmed by the goodwill of those who have learned about Winry’s situation.
Every younger sister wants to have an older brother like Asher looking over her. And in Winry’s case, Asher is a genuine, caring, and nice brother. According to Nicole, he is incredibly oblivious to the fact that she is anything “special.” He understands she has a birthmark on her face; however, it is nothing special to him than having different eye colors.
Asher, like other children of his age, may be jealous to share his mother’s attention, but Nicole is certain he will become both Winry’s best friend and guardian.
Nicole and her spouse do everything they can to safeguard and raise Winry and her brother to be confident in all of their abilities and characteristics every single day. They’re concerned about how others may perceive or judge Winry, just as much as they are about how she is doing physically.
Nicole has informed us that one of their highest goals in life is to teach Winry to appreciate values such as compassion. They are attempting to raise her into a warrior, constantly reminding her of her attractiveness in the hopes that Winry will grow up to be as happy as she is now.
Nicole is confident in the fact that they will always take care of and steer their daughter toward individuals who would treat her with respect and kindness. Winry’s family will always be there to protect and guide her — that is what matters most.
Nicole is dedicated to raising CMN awareness via social media; her primary objective is to educate the general public about Winry’s condition while also urging parents to instill in their children a perspective of appreciation for difference and their own positive qualities.
Winry is the first member of her family to have this birthmark, as Nicole had said, and despite its rarity, there are far too many families who can relate to and benefit from Winry’s tale.
They will try anything to make their daughter’s life path as pleasant as possible. Nicole has made it her duty to educate and normalize the public’s perception of birthmarks. They anticipate that Winry will have to depart somewhere, meet someone new, and endure a barrage of inquiries about her appearance; they want to make things better for Winry and other youngsters like her.
