Lisa Lee, 25, was sleeping next to her husband Lewis Little when she thought she heard him snoring. “I shoved him out of bed to stop what I believed was snoring,” Lisa explained. But as she touched the moist sheet, she knew something wasn’t right. Lewis wasn’t breathing. “I turned on the light and stared at his battered face,” she added.
Panicked, Lisa called for an ambulance, but the wait felt endless. When medics arrived, they broke the heartbreaking news: Lewis had passed away hours earlier. The sound Lisa had mistaken for snoring was, in fact, air escaping his body and passing through his vocal cords.
Lewis had been diagnosed with Brugada syndrome, a rare heart condition, just a year earlier. Doctors had assured him that his life wasn’t in danger and that he could live a long life despite the condition. Tragically, just a year later, Lewis died unexpectedly in his sleep.
Lisa was left in shock. “I couldn’t believe it. The doctors told us he was going to be fine,” she said, still processing the sudden loss of her husband.
Brugada syndrome is a genetic condition that affects the heart’s rhythm and can lead to sudden death. In Lewis’s case, it proved fatal despite earlier reassurances.
Determined Mom Sets Out to Show Her Child She’s Beautiful, Despite a Unique Birthmark
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.
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