This story is a sobering reminder of the resilience of the human spirit and the long road society has to travel toward kindness and acceptance. It is about a little boy who endured a devastating attack by two Rottweilers and survived, only to face cruel judgment from others due to his disfigured appearance.
Ryder Wells was just 21 months old when the unthinkable happened. During Thanksgiving of 2015, Ryder and his mother, Brittany, were visiting family friends. Brittany recounted the horrific incident:
“We were eating breakfast, and Ryder was moving back and forth between his toys and coming back for bacon. Then, he disappeared. I looked out of the window, and he was face down in the garden.”
She continued, “He had pajamas on, but they’d been completely ripped off except for a sleeve. When we picked him up and rolled him over, his face was just gone.
“The dogs had been around him before, and they’d been fine, so I don’t know what happened. The doctors said they would do what they could, but we weren’t expecting him to make it. They told us it’s a miracle he’s still here because he was so small, and the injuries were so severe. They thought the dogs had bitten so far into his skull that he would be paralyzed.”
Ryder’s injuries were catastrophic: he lost his entire right cheek, more than half of his lip, his teeth were crushed, his right lung was punctured, and his arm was broken. He was airlifted to the hospital, where he underwent over 14 hours of surgery. For Brittany, it was an unimaginable ordeal filled with anxiety and uncertainty.
Despite the severity of his injuries, Ryder’s spirit proved unbreakable. He survived the surgeries but was left with a permanently disfigured face. Over the years, he has undergone more than 50 facial reconstruction surgeries, with more to come in the future.
However, Ryder’s battle is not just physical. He faces the harsh reality of societal judgment. Brittany shared:
“He knows people are talking about him, but he doesn’t say much. He wears glasses and a cap and sometimes hangs his head to hide his face. I try to deal with it in a way that doesn’t affect him too much. I tell him every day that he’s beautiful, that different is beautiful, and it’s okay to be different.
“But I’m absolutely terrified about when he goes to school. There are always going to be a few kids who aren’t kind. When he started kindergarten, the kids learned about Ryder before they met him so they wouldn’t be as shocked. You always want your kid to be accepted and to fit in. Just because he’s different doesn’t make him any less of a person.”
Despite the challenges, Ryder has found a supportive community. Brittany expressed gratitude for the kindness they’ve encountered:
“He has a great group of friends, and people in town know him now, which boosts his confidence. He’s been amazing in how he’s adapted after everything he’s been through.”
Now five years old, Ryder’s journey is far from over. His family has started a GoFundMe campaign to support his future surgeries and treatments. Ryder’s story is a testament to his incredible resilience and a call for greater kindness and empathy in the world. We wish Ryder a life filled with love, acceptance, and opportunities to thrive despite the challenges he has faced.
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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