Even though twins aren’t that rare, people are always intrigued by how two people can look so alike.
I’m fascinated by it too…
But Megan and Morgan didn’t just catch people’s attention because they looked alike. When they were four years old, their eyes were so clear they looked like crystal water. Once their photos were shared online, they quickly went viral.
Megan and Morgan Boyd, known as the “Trueblue Twins,” became famous when they were just four years old. Their mom shared photos of them on Instagram, and people around the world fell in love with their unique look.
While most parents enjoy showing off their kids’ pictures, these twins caught global attention. Now, they have over 153,000 followers on Instagram.
It’s easy to see why, isn’t it?
The girls were born on June 6, 2011.
Their mom, Stephanie, came up with the nickname “Trueblue Twins” because of their special blue eyes.
If you want to tell Megan and Morgan apart, just look at their eyes—they’re the key to distinguishing them.
It’s only Megan who has two blue eyes. Morgan’s right eye is not blue, but dark brown and thus bears a completely different look.
This is how the girls look today at nine years old.
Many twins often wear matching outfits, and the Trueblue Twins are no exception.
Their mom, Stephanie, loves shopping for clothes for her daughters and keeping their wardrobes current.
She thinks it’s important for her twin daughters to look and feel great.
Many people are amazed by the girls’ rare blue eye color.
Some folks might think African-American adults with blue eyes are wearing colored contacts, but it’s possible to be born with a rare gene that gives blue eyes.
Stephanie, the Trueblue Twins’ mom, also has blue eyes, and she says she doesn’t wear colored contacts.
Even though her daughters have become social media stars, Stephanie stays grounded.
She understands that Megan and Morgan’s natural beauty could lead to modeling careers, but she doesn’t want to push them into something they might not enjoy. That’s smart!
Just look at these beautiful 11-year-olds today—aren’t they stunning?
Everything indicates that these lovely sisters will grow up to be beautiful women. Feel free to share this story if you believe the same.
A baby with a rare skin disorder is born after an urgent C-section by medical professionals.
Throughout the nine months of pregnancy, a mother’s heart is filled with anticipation, excitement, and a hint of doubt. When an expecting parent gives birth, they all want the child to be healthy and happy. Regretfully, our expectations are not always met by the way things work out.
Jennie Wilklow, of Highland, New York, was looking forward to meeting her daughter. Jennie and her spouse were overcome with happiness the moment they held their baby.
After multiple ultrasounds and check-ups with the physician, the results consistently showed a healthy baby.
This assurance put their minds at rest, and they had no idea that their darling Anna would be born with a disease that would permanently alter their lives.
At 34 weeks, Jennie had a C-section to deliver Anna. She peered into Anna’s eyes when the physicians placed the baby in her arms and felt an overwhelming sense of love.
Everything was going fine with their cute little one. However, Jennie couldn’t help but feel apprehensive about her husband when he came to visit her.
Jennie told Cafe Mom, “My husband’s silence scared me.” I pressed him for additional information as the doctor was leaving the room, and he just sat there looking shocked. With remorse, he added, “It’s bad.”
Upon meeting her gaze, her spouse said, “Jennie, she has the most beautiful soul.” Jennie did not know what such terms meant at the moment. Her mind was racing, but she had no idea what was wrong.
Anna suffered from an uncommon disease known as harlequin ichthyosis, which showed up as thick, severely fractured diamond-shaped plates. Jennie said to Cafe Mom shortly after giving birth, “Her delicate skin hardened as they desperately tried to help her.”
The dramatic splitting that followed the hardening left her slathered in open wounds throughout her body.”Anna prevailed despite the physicians’ concerns about her prognosis. She was quite beautiful,” Jennie proudly declared.
Unfortunately, there is no known cure for harlequin ichthyosis. The treatment involves regular showering and thorough skin moisturization, which takes consistent effort. I used to bathe her for hours every few hours, slathering her in Vaseline.
It might not seem like much, but it was one of the things I struggled with the most. I had visualized all the amazing clothes my child would have,” Jennie said.
She set up the “harlequin diva” Instagram page and started posting images of Anna there in an effort to raise awareness of this illness. Through her articles, she sheds light on the challenges faced by parents of children with harlequin ichthyosis on a daily basis.
“Anna won many people’s hearts and is the pinnacle of perfection in its purest form.” She has a natural capacity to carry out these mundane tasks. The world celebrates with us every time we achieve a new milestone, Jennie said to Cafe Mom.She went on, “I now realize that my love for my daughter is the reason Anna was given to me.” Because we were destined to be together, we will work together to redefine what true beauty means to the world.
In addition to being beautiful in her own right, Anna is fortunate to have parents who will stop at nothing to ensure that she has a happy existence.
Let’s help spread the news about Anna’s story by inviting our friends and family to read this article on Facebook. Despite our differences, we can work together to raise awareness of and respect for the incredible beauty and power that each individual holds.
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