Ask any parent and they’ll likely tell you there’s nothing they wouldn’t do for their child.
Becoming a mother or father changes life in ways that are hard to explain. From that day on, parents dedicate themselves to loving, caring for, and worrying about their child for the rest of their lives.
Sadly, though, there are some things even parents can’t prevent. Accidents and illness are part of life, and too many children suffer from things they can’t control.
Alina and Aaron Edwards’ lives were turned upside down when they learned that their 9-year-old daughter, Emma, had acute lymphoblastic leukemia. Heartbroken, they held onto hope that Emma could fight the cancer. But after a few months, doctors delivered the devastating news that there was nothing more they could do to save her.
Determined to make the most of the time they had left, Emma’s parents decided to fulfill her wishes.
Many children in such situations might want to meet a celebrity, visit Disneyland, or walk out onto a sports field with their favorite player.
But Emma’s wish was different. She wanted to marry her 10-year-old boyfriend, DJ.
Before long, Emma’s wish gained a lot of attention from her local community. Volunteers and supporters came together under the name “Emma’s Army,” all working towards making the little girl’s dream come true before her time ran out.
The Make-A-Wish Foundation eventually stepped in to help Emma’s family raise funds. Emma’s mom, Alina, explained, “Most kids want to go to Disneyland, but Emma wanted to get married, be a wife, and have three kids.”
Reports say this wasn’t the first time Emma and DJ tried to marry each other. At the age of eight, the two had attempted to have a wedding at school. They even picked out bridesmaids and groomsmen from their classmates. However, their teacher didn’t allow the “wedding,” no matter how unofficial it was.
This time, though, the wedding had the full support of their parents and the help of countless kind-hearted people who were determined to make Emma’s wish come true.
“We put it all together in less than two days, and everything was donated. It was so precious, and it came together perfectly,” Alina shared.
When the big day arrived, the special moment was captured on video, including interviews with some of the guests. The young groom, DJ, shared his feelings, saying, “I thought she was the most beautiful person I ever saw. Ever since, I loved her.”
Emma’s mom, Alina, also had heartfelt words for DJ, expressing her gratitude for her daughter’s caring friend. In an emotional Facebook post, she wrote:
“DJ has been Emma’s ‘Boo bear’ since 3rd grade, and seeing these two together will melt your heart. DJ protects her, helps her, and makes her heart soar. She loves him, and I know he loves her too! He’s stood by her side through all the ups and downs and kept her smiling. DJ will forever be family.”
On June 29, Emma’s dream wedding became a reality. Arriving in a wheelchair, pushed by her loving parents, Emma wore a stunning purple dress and smiled brightly as her father escorted her down the aisle.
Emma and DJ exchanged rings and vows, with DJ sealing the ceremony with a sweet kiss. After the wedding, Emma returned to rest in bed, but her joy from the day was clear to everyone who saw her.
Sadly, just a few weeks later, on July 11, 2023, Emma passed away after bravely battling leukemia.
Her obituary read: “Emma Brooks Edwards entered heaven and into the loving arms of her Great-grandma Frannie Annie on July 11, 2023, surrounded by those who love her most. Emma was 10 years old and battled leukemia for 16 months. Our little unicorn, Emma, was born on April 22, 2013, and completed the Edwards family. She loved arts and crafts, practical jokes, her family, friends, Jesus, and her newlywed ‘husband,’ DJ. Emma was a light to all who knew her and an inspiration to everyone she met. She was the best daughter, sister, granddaughter, niece, cousin, aunt, ‘wife,’ and friend. Her legacy is one of strength, humor, and endless love for all.”
Rest in peace, Emma, a beautiful soul taken far too soon.
Mom of rare twins with Down syndrome shuts down critics with photo showing how beautiful they are
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.”
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