Twin pregnancies are still quite uncommon, despite a 72% increase in likelihood between 1980 and 2018. Twins are born in about 33 of every 1,000 births.
What are the probabilities of having identical twins? Out of 1,000 births, three to four are identical twins on average. So once more, not very common.
Savannah Combs, age 23, was overjoyed to learn she was expecting twins. She then discovered that they both have Down syndrome, which is also unusual.
Of course, the information was upsetting. Savannah and her husband Justin Ackerman were aware that due of her illness and the state of her children, some people would judge them.
But Savannah finds that to be the same thing that makes them so beautiful.
“It’s very rare what they have, but they’ve been my little gems,” she mentioned.
Savannah, a Middleburg, Florida native, posted videos of her postpartum journey on TikTok with her kids Kennadi Rue and Mckenli Ackerman, and the videos immediately acquired popularity.
Savannah said in one of her videos that she was advised to abort her children because they wouldn’t survive.
She made the choice to keep them and give them a shot.
”Every [prenatal] appointment they were alive was a blessing to me,” Savannah explained.
Her spouse was gone at boot camp when she found out they both had Down syndrome.
When Savannah was admitted to the hospital, she was 29 weeks along with her pregnancy and gave birth to twin daughters. Kennadi Rue and Mckenli Ackerman, identical twin daughters, were born on May 12, 2021.
The twins had to spend a few weeks in the NICU before going home because they were born two months early.
“They’re called mono di twins, meaning that they had their own sacs, but they shared the same placenta, meaning that they were going to be identical,” she said.
“Mo di twins as it is, it’s like very rare. And then you throw Down syndrome on top of it, it’s like one in 2 million.”
They are just like any other youngster, according to Savannah, despite having an uncommon disease.
“They have feelings. They have a beating heart. They know how to talk. They know how to do things you do. They will get there,” she said.
“Like I said, it may be a step behind but they’re going to do it. I’ve learned these kids are feisty little things and happy little things.”Savannah posts wonderful updates on TikTok as each youngster continues to reach their milestones.
“I’m going to let them know that they’re just like us and they’re going to get there as long as they put their minds to it.”
Nevertheless, some people feel compelled to be critical of Savannah and her family. The young mother was forced to respond to some extremely cruel people on social media as a result.
”I wouldn’t want those babies; if mine came out like that, they would be straight up for adoption,” one person wrote to the mother.
Savannah, though, had the ideal response, which she posted on Facebook.
“I said, good thing they weren’t born to you and were born to me. God knew what he was doing by giving these babies to the right parents who would love them regardless.”
Baby with White Hair Overcomes Challenges and Shines with Happiness
Any parent would be happy to have a newborn, and Patricia Williams was no different. She thought her baby Redd was perfect when he was brought into the world. She had no idea that his unusual features would present obstacles as well as opportunities for success in the years to come.
Patricia and her husband Dale became aware of their son’s lateral eye movements when he was only two months old. Fearing for their lives, they searched Google and discovered something unexpected: it might be an indication of albinism. One in 17,000 individuals worldwide suffer with albinism, an uncommon disorder marked by pale complexion, white hair, and tracking eyes.
Patricia and Dale sought a formal diagnosis, and after consulting with experts, it was determined that Redd had Oculocutaneous Albinism Type I (OCA1). The pair was surprised since they were unaware of this illness. However, this realization was only the start of their adventure.
Redd’s unusual features presented difficulties as he grew older. He was the victim of bullying at school, but fortunately, his elder brother Gage stood up for him. When Patricia’s second son, Rockwell, was born with the same issue, her early hopes that Redd would outgrow his unique qualities were dashed.
The difficulties persisted after that. Rockwell’s photos were twisted into cruel memes on social media, adding insult to injury for the family. However, Patricia and Dale took a bold choice rather than focusing on the negative. They made the decision to become activists for albinism, spreading knowledge to stop bullying of other kids who have the illness.
Patricia became determined to spread awareness about albinism after realizing that most people had limited understanding of the condition and that uncommon films and scant representation had largely shaped people’s opinions. She recognized that she had a rare chance to dispel myths and raise awareness of this illness.
Redd’s strabismus was treated with eye surgery in order to improve his condition. The procedure worked, and Redd did well when he went from attending a school for the blind to a public one. He accepted himself and his special qualities with the help of his devoted family and friends.
Redd and Rockwell are still happy now and continue to shatter stereotypes. Apart from needing a hat, sunglasses, and sunscreen when playing outside, they are just like any other kids in the world. Love and adoration for Patricia’s latest video of Rockwell during his school’s “Western Day” went viral on social media. His charming beauty and the characteristic light blue eyes of an albino person grabbed the attention of many.
Patricia’s message of love, acceptance, and understanding is evident despite the difficulties of the voyage. The tale of this family inspires us all and serves as a reminder that individuality should be valued rather than disparaged.
The next time you come across someone special, stop to hear their tale and show them some love. We can make the world more compassionate and inclusive if we work together.
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