We are all born unique and beautiful, each one of us an individual expression of diversity. One of the most incredible aspects of being human is that no two people are exactly the same. Over time, society has made great strides in embracing and celebrating these differences.
Nicole Lucas Hall, a devoted mother, is raising her two children, Asher and Winry, with a mission to challenge the idea that imperfections define us. Nicole wants to reinforce the belief that her daughter Winry, who was born with a rare birthmark, is beautiful in her own right.
Winry was born with a condition known as congenital melanocytic nevi (CMN), an uncommon birthmark that covers about a quarter of her face. According to Good Morning America, Winry’s distinct appearance has made her stand out since her birth in February 2021, though her parents embrace and celebrate her uniqueness.
Determined Mom Sets Out to Show Her Child She’s Beautiful, Despite a Unique Birthmark
byBrowse Feed–October 14, 20240
We are all born unique and beautiful, each one of us an individual expression of diversity. One of the most incredible aspects of being human is that no two people are exactly the same. Over time, society has made great strides in embracing and celebrating these differences.
Nicole Lucas Hall, a devoted mother, is raising her two children, Asher and Winry, with a mission to challenge the idea that imperfections define us. Nicole wants to reinforce the belief that her daughter Winry, who was born with a rare birthmark, is beautiful in her own right.
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Winry was born with a condition known as congenital melanocytic nevi (CMN), an uncommon birthmark that covers about a quarter of her face. According to Good Morning America, Winry’s distinct appearance has made her stand out since her birth in February 2021, though her parents embrace and celebrate her uniqueness.
Nicole, a teacher, recalls being initially shocked when the nurses handed her Winry after delivery. Her pregnancy had been normal, so she wasn’t expecting anything unusual. “I had a typical pregnancy,” Nicole wrote on her blog. “After some early morning sickness, I felt great until the last month when fatigue kicked in.”
The medical team was the first to notice Winry’s CMN, but they offered congratulations for the easy birth and reassured Nicole that her baby’s vital signs were fine.
At first, Nicole mistook the large mark on Winry’s head for a bruise. “My husband and I quickly realized it wasn’t a bruise,” she said. “I thought it looked like a mole.” Concerned but unsure what to ask, Nicole held her baby close and showered her with love.
CMN can appear as dark or light brown patches on various parts of the body, and its size can vary, according to the National Organization for Rare Disorders.
Now, Nicole and her partner are on a mission to show the world that differences should be celebrated, not hidden.
“I like sharing because, for many, this is the first time they’ve seen a birthmark like hers,” Nicole said. “Parents can have meaningful conversations with their children about how kids can look different, or they may see their own child reflected in Winry.”
Winry’s parents take extra care of her skin, as her birthmark may increase her risk of melanoma, a form of skin cancer. “Our main concern is her health,” Nicole explained. “We make sure to use sunscreen and keep her protected with hats.”
Beyond her birthmark, Winry is a joyful and spirited little girl who radiates happiness. “She’s the happiest baby I’ve ever seen,” Nicole said. “She’s always laughing and yelling, and she’s already showing signs of having quite the personality!”
Nicole hopes that by sharing Winry’s story, more people will embrace differences rather than mock or belittle them.
To her, Winry is not just a child with a unique appearance—she’s a truly special little girl with a beautiful spirit.
The Tragic Reason Why One Man Actually Turned Blue Forever
The world’s most famous blue man, Paul Karason, also dubbed Papa Smurf, was born as a fair-skinned, freckled boy with ginger hair. In the 2000s, he became an internet sensation and made many TV appearances, openly talking about his condition. Let’s find out together why Karason turned blue and how he became a cautionary tale.
Paul Karason had a skin condition that made his skin flake, as well as acid reflux and arthritis. Doing his own research in order to improve these ailments, he found out about a solution of silver in water, also known as colloidal silver.
Colloidal silver was widely used as an antibiotic back before penicillin was invented in the 1930s. It was banned in 1999 in over-the-counter medications after scientists found that it can severely damage internal organs.
The late Paul Karason and his wife, Joanne
Karason drank what he believed was a miracle cure for over 10 years. Moreover, he even began to apply a silver preparation directly to his skin; he claimed his acid reflux and arthritis just went away. “I had arthritis in my shoulders so bad I couldn’t pull a T-shirt off. And the next thing I knew, it was just gone,” he shared.
Due to the silver accumulation in his skin, he started to turn blue and suffered from a permanent and rare condition called argyria. Only when Karason met an old friend who asked him, “What have you done to yourself?” did he begin to realize he’d become blue.
Karason claimed his blue skin had many advantages — he never got sunburns or had to wear sunglasses. There were some side effects he did not appreciate, however, such as folks “being less than polite” to him. Moreover, Karason confessed he couldn’t get a job because of employers’ resistance to hiring “people that are blue or that are noticeably different.”
Sadly, Paul Karason passed away in 2013 when he was 62 years old due to heart complications.
Papa Smurf’s story serves as a valuable lesson about the importance of being careful when it comes to at-home remedies. While it’s natural to want to find easy solutions to health problems, it’s important to be aware that such remedies can sometimes pose serious risks. It’s always better to consult a doctor and follow their advice for a safe and effective treatment.
Preview photo credit Inside Edition / YouTube
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