Hurricane Helene, the deadliest mainland storm since Katrina in 2005, has claimed the lives of 200 people as rescuers continue their search for survivors. The deaths have been reported in South Carolina, Georgia, Florida, North Carolina, Virginia and Tennessee.
The number of people missing is counted in hundreds, and the number of homes left without electricity is nearly a million. Unfortunately, rescue teams face challenges as many roads rendered impassable by the storm’s destruction.
North Carolina Governor Roy Cooper highlighted the severity of the situation, saying that the rugged landscape has made it difficult for many communities to receive any assistance.
Among those who lost their lives is 7-year-old Micah Drye of Asheville, North Carolina. He and his grandparents were swept away by floodwaters after seeking refuge on a rooftop. The boy’s mother, Meghan, survived.
The news of Micah’s death was disclosed by his aunt, Jessica Drye Turner, who also shared the boy’s final words, “Jesus! Please help me!”
The heartbroken aunt expressed her grief and pain over the loss of her sister’s son. “New grief and strong faith. New motto.”
The boy’s lifeless body was located about a quarter mile from where his mother had been rescued.
Meghan’s other sister, Heather Kephart, started a GoFundMe page to help Meghan after the devastating loss of her son, her parents, and all her belongings, including her home.
The fundraising page included a photo of sweet Micah, taken by his grandmother mere days before the tragedy. He could be seen wearing a Jurassic World T-shirt and smiling.
This family’s huge loss is just one of many caused by the devastating storm.
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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