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.
Parents were really surprised when their baby was born with a big smile on its face.
Ayla Summer Mucha startled her parents by beaming brightly when she was born in December 2021. Her parents fell in love with her right away, despite their first confusion due to an unusual illness that caused her smile to be permanent. Ayla is now well-known on social media, and her charming smile is adored by people everywhere.On December 30, 2021, Cristina Vercher and her husband Blaize Mucha were eager to finally see their newborn girl after nine months of waiting. However, unexpected news was delivered by the doctors during the C-section delivery.Due to bilateral macrostomia, Ayla Summer Mucha’s mouth did not form normally from birth.When a baby is growing inside its mother, the corners of the mouth sometimes don’t meet correctly, a condition known as a facial cleft. Just 14 cases similar to it have been documented in medical books due to its extreme rarity.Because the ultrasounds revealed no issues, Ayla’s parents were unaware of this until after she was born. They became really concerned when they noticed that she was speaking with her mouth agape. Even though Ayla was so small, the problem was evident, which startled and worried Ayla’s parents, who are now 23 and 22 respectively.”I had never met anyone born with a macrostomia, and neither Blaize nor I knew about this condition,” Adelaide’s Vercher remarked. Thus, it came as a huge surprise.Not just the parents expressed surprise.
A baby with bilateral macrostomia was beyond the capabilities of even the medical professionals.The fact that it took hours for a doctor to respond to our questions made it much more concerning. She added that the hospital was also ignorant of this uncommon ailment. “As a mother, all I could focus on was my mistakes.”However, medical professionals informed the anxious parents that there was nothing more they could have done. Cristina was concerned that she might have erred during her pregnancy or contributed to her daughter’s illness.She remarked, “I couldn’t stop wondering where I might have made a mistake as a mother.” They were convinced, nevertheless, that they had no influence over this problem and that they were not to blame following days of genetic testing and scans.The Mucha family concentrated on assisting Ayla in managing her illness, which limits her food and drink options, comfortably. Babies with this illness occasionally require surgery to become better.Ayla’s parents posted her story on social media so that people may learn more about it. Around 6.5 million users enjoyed Ayla’s adorable smile on TikTok. The amount of support that the Muchas received shocked them.”I just looked it up, and there are only 14 cases like hers that are known,” a commenter said. She is truly unique. Mom, you ought to feel proud.Regarding Ayla’s smile, another internet user stated, “She is gorgeous and just perfect the way she is.” Her smile made me smile as well.But nasty things about Ayla were said by several people online. But Ayla’s supporters swiftly came to her aid.”Your daughter is stunningly gorgeous. Never pay attention to such nasty folks. One individual remarked, “She’s like an angel.” Someone else posted, “Oh my gosh! You’re quite adorable! Pay no attention to their hurtful remarks. You’re simply too cute.”You’re a strong mom, and your daughter is beautiful,” commented another commenter. I apologize for exposing you to those hurtful remarks.Vercher said, “I think it’s important to be kind and accept everyone, no matter what,” to the hurtful remarks made about her child.If she and her child were in a similar circumstance, she hoped that people would treat them with the same respect. Vercher said that anyone could experience similar circumstances. She added that since you have no control over what other people say on social media, it can be a difficult place.Vercher ignored the criticism in favor of highlighting the encouragement and kind remarks. “We’re really proud of ourselves, so we won’t stop sharing our experiences and favorite memories,” she remarked.
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