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.
Greedy Heirs Tried to Earn Favor with Grandpa to Inherit More, Their Jaws Dropped When the Lawyer Read the Will
“You always have room for one more,” his late wife would say with a gentle smile. Mr. Lewis believed in giving back and creating a life of meaning through acts of kindness.
But in his later years, the family that had once filled his home with joy grew distant. His children rarely visited, except when they needed something.
“Dad, it’s tough out there. Just need a little help,” his eldest son, Richard, would say, barely making eye contact before asking for money.
Olivia, his daughter, was no different. “Dad, the kids’ school fees are outrageous. Could you—” she’d start, and before long, he’d be reaching for his checkbook.
Even his grandchildren only came around during holidays, eyeing his home and wealth more than they ever looked at him.
When Mr. Lewis received his terminal diagnosis, he called his family to share the news. Within hours, they flocked to his mansion, putting on their best performances as the “devoted” children and grandchildren.
“We’re here for you now, Dad,” Richard said, patting his father on the shoulder with forced affection.
“We’ve got you, Grandpa,” echoed his teenage granddaughter, Willow, her eyes barely leaving her phone as she spoke.
For weeks, they hovered around him, offering tea they hadn’t brewed themselves and empty words they didn’t mean. Mr. Lewis saw through it all. They weren’t there out of love—they were there for the money. He was no fool, and though his heart ached, he knew exactly what was happening.
When Mr. Lewis finally passed away peacefully in his sleep, the family immediately shifted their focus to the inheritance. The day of the will reading, they packed into the lawyer’s office, eager to claim their share.
“I bet Dad left the most to me,” Olivia whispered smugly.
“Please,” Richard scoffed. “I’m the one with the business sense.”
But the bickering ceased when Mr. Alaric, the family lawyer, entered the room—accompanied by a quiet, 13-year-old girl none of them recognized.
“Who’s the kid?” Richard blurted out, his confidence fading.
“This,” Mr. Alaric announced, “is Harper. She’s here for the reading of the will.”
Confusion rippled through the room as the family exchanged puzzled looks. The lawyer’s next words left them speechless.
“Harper is the sole heir to Mr. Lewis’ entire estate.”
The room erupted into chaos. “What are you talking about?!” Richard shouted. “She’s just a kid! Dad would never do that.”
Olivia’s voice rose in disbelief. “This is absurd! We’re his family—his blood!”
Mr. Alaric raised his hand for silence. “I know this is a shock, but Mr. Lewis left a letter explaining his decision. Allow me to read it.”
The room fell silent, thick with tension, as the lawyer began.
Dear Family, the letter began, I know you’re probably confused, maybe even angry. But please hear me out. Over the past few years, Harper has been my greatest source of joy. She’s the little girl who lived next door. Long before any of you noticed, Harper saw that I wasn’t well. She’d see me struggling to get the mail or sitting alone on the porch.
Harper shifted uncomfortably as all eyes turned toward her, but she stayed quiet, her hands clasped.
Harper visited me every day. Not for money, not for favors. She came to share stories, play cards, or just sit with me. She made me feel less alone. In the years when I needed family the most, Harper was there.
Richard rolled his eyes. “We were busy living our lives, Dad. You should’ve told us you were lonely.”
Ignoring the interruption, Mr. Alaric continued reading.
What you don’t know is that Harper has her own battles to fight. A few months ago, she was diagnosed with a terminal illness—one no child should ever have to face. Despite her struggles, she’s remained a light in my life. She deserves the chance to live her dreams, no matter how short her time may be.
A stunned silence fell over the room as Mr. Lewis’ children absorbed the revelation. Even Olivia, who had been fuming moments earlier, sat quietly, tears welling in her eyes.
By the time you hear this, I’ll be gone. Harper may only have a year or two left, but I’ve made sure she has everything she needs to live those years to the fullest. Instead of fighting over my money, I hope you’ll support her in the way she supported me. Harper showed me love when none of you did. Remember: love is the greatest inheritance.
Mr. Alaric folded the letter, leaving the room heavy with the weight of Mr. Lewis’ words.
Harper stepped forward, her voice small but steady. “Mr. Lewis was my friend. I never wanted his money, just his stories and time.”
Richard cleared his throat, ashamed. “Harper, I’m sorry. We didn’t know…”
“I’m going to use the money to travel with my parents, eat ice cream for breakfast, and live as much as I can,” Harper said. “When I’m gone, the rest will go to other kids who are fighting like me.”
Tears streamed down Olivia’s face. “You’re so brave, Harper. I hope you get to do everything you dream of.”
Over the following months, Harper did just that. She visited the Eiffel Tower, dipped her toes in the ocean, and filled her days with laughter and love. When her time came, she passed away peacefully, surrounded by those she loved.
True to her wishes, the remainder of Mr. Lewis’ fortune was donated to charities that supported children with terminal illnesses, funding research and helping families in need.
Harper’s legacy became a symbol of the power of kindness and the impact of genuine connection. And for Mr. Lewis’ family, the lesson was clear: wealth isn’t measured by money, but by love. Harper had taught them all the true value of life.
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