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.”
Emma Heming Shares Emotional Video of Bruce Willis Following Dementia Diagnosis
Following his diagnosis with aphasia, a condition that disrupts communication, actor Bruce Willis has largely stayed out of the public eye. His family has been candid about his condition, revealing that he has frontotemporal dementia (FTD) and continues to keep fans updated on his health journey.
Rumer Willis, Bruce’s daughter, took to social media to express the family’s gratitude: “We want to start by thanking everyone for the overwhelming outpouring of love, support, and the wonderful stories we have received since sharing Bruce’s initial diagnosis. With that in mind, we wanted to provide an update on our beloved husband, father, and friend, now that we have a clearer understanding of his condition.”
She added, “Since we disclosed Bruce’s aphasia diagnosis in spring 2022, his condition has progressed, leading to a more specific diagnosis: frontotemporal dementia (FTD).”
As Bruce’s cognitive abilities continue to decline, his medical team is doing all they can to make his life more comfortable. Emma Heming, Willis’ wife, is working closely with a dementia specialist to ensure that the Die Hard star receives the best possible care. “My grief can be paralyzing, but I’m learning to coexist with it. As my stepdaughter, Scout Willis, reminded me, grief is the purest form of love. I hope that brings you some comfort too,” she shared in 2022.
Recently, Emma discovered a new Instagram feature that showcases past photos and videos. She shared a memory of Bruce from a year ago, where he is seen praising her, with the caption: “What’s this new Memory feature on IG!? Omg, my biggest fan. I’m so in love with him.”
In the video, Bruce is heard expressing his admiration for Emma’s skincare brand, Cocobaba.
Before the family publicly disclosed Willis’ diagnosis, his colleagues observed that he was struggling to remember his lines. A crew member from his recent film, White Elephant, remarked: “It wasn’t a matter of annoyance but more about protecting Bruce’s dignity. Someone would feed him a line, and he struggled to grasp its meaning. He was just being guided along.”
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