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.
Mom of Boy with Rare Condition Shares Their Life, People React Differently
Logan Pacl stands out among teenagers. At 17, he faces a rare illness known as Sanfilippo syndrome. Often called “childhood Alzheimer’s,” this cruel disorder gradually takes away a child’s cognitive skills, mirroring the effects of Alzheimer’s in older people. But he keeps fighting and uses social media to spread awareness about his condition.
At first, everything seemed normal.
Logan Pacl’s life is a battle against time. Diagnosed with Sanfilippo syndrome, often known as “childhood Alzheimer’s,” the 17-year-old from Silverdale faces a relentless genetic disorder that viciously strips away the very essence of childhood. Caused by a single defective gene, this neurodegenerative disease attacks the brain and spinal cord, leaving behind a cruel wake of lost abilities, seizures, and constant pain. It’s a ticking time bomb, as most children with this terminal illness don’t survive beyond their mid-teens.
For Logan’s family, the heartbreak began early. Born in 2007 with his twin brother Austin, Logan seemed like any other healthy baby. Both boys hit their developmental milestones—until Logan began to fall behind. A year in, the red flags emerged: while Austin was speaking, Logan remained silent. The difference between the brothers grew, signaling the start of a devastating journey.
Sanfilippo syndrome doesn’t just rob children of their future—it erases their past.
Then the news of the diagnosis hit the parents, something no one could have anticipated.
As Logan’s condition worsened, with chronic infections and a noticeably swollen belly, Noelle and William were left searching for answers. In January 2010, they learned that Logan had Sanfilippo syndrome, a terminal illness with no cure or treatment, and a life expectancy that typically extends only into the late teens. “I’ll never forget the day we got the phone call. The genetic counselor on the other end went on and on, and all I thought was, well get to the part on how we fix this. Then she said it, ’This disease is terminal, and there is no cure or treatment,’” his parents recall.
Noelle recalled her initial reaction, grappling with the news that the disease was terminal. The weight of the diagnosis was overwhelming, leaving her with a heart that felt as though it had dropped into her stomach. The severity of the situation rendered her unable to process much beyond the devastating reality.
Noelle described the experience of mourning not just the child she had but the life she had envisioned for him, a life that was abruptly stolen away. The medical advice they received was minimal and unhelpful, simply advising them to take Logan home and cherish their time with him. This lack of concrete guidance only deepened their sense of helplessness.
In their search for hope, Noelle and William discovered an experimental stem cell transplant through online research. Inspired by the success of another mother’s child, they decided to pursue the same treatment for Logan. So, Pacl went through a tough three-month treatment that was basically a bone marrow transplant. He had to endure chemotherapy to wipe out his immune system so it could accept the new stem cells. It was a risky procedure, but it seems to have helped with some of Logan’s physical symptoms.
His mother uses social media to spread awareness about his condition.
At 17, Logan’s life is very different from that of most teenagers. Losing his ability to speak at a young age was tough for him and his family, but over time, he’s become more easygoing. “Life with Logan is anything but typical. Each day is a battle to maintain the skills he still has,” his mother Noelle said.
Since 2020, Noelle has been a vocal advocate for Sanfilippo syndrome, using TikTok to share her family’s story. Her videos have reached a global audience, raising awareness about the disorder and encouraging other parents to seek early diagnosis for their children.
Although Logan’s future is uncertain, the Pacl family is committed to making the most of their time together. Noelle and William used to avoid thinking about what lies ahead, but now they focus on cherishing every moment with Logan and ensuring he enjoys his time to the fullest. Noelle notes that among Sanfilippo parents, there’s a bit of a joke that all their children seem like siblings, sharing similar features like bushy eyebrows, a low nasal bridge, and large, round stomachs.
Even with the demands of caring for Logan, Noelle keeps life as normal as possible for Logan’s siblings, Austin and Aidyn. She acknowledges that having a brother with special needs can bring its own set of benefits.
As for sharing Logan’s journey online, Noelle remains thoughtful about what she posts. While she plans to continue sharing, she’s careful to respect her family’s privacy. “We just live in the moment,” his mother said. “And if something comes up, and we’re like, we can make that, we’ll do it.”
People in comments react differently.
Mostly people express support and empathy.
- You take the most wonderful care of him. You are the greatest mom. © lauralang1108 / Instagram
But some show a bit of skepticism.
- Genuine question, what is your plan when you are gone? © devin_abq.505 / Instagram
- I just wanna know why it’s necessary. People have to publicize their children’s conditions. Why do people think that we all wanna know what’s wrong with your child? I feel sorry for the parents, but I don’t know why you want to put this all out there. I’m sure you have support group publicizing putting your child out there like this. © marlawomble / Instagram
Today, conversations about living with disabilities are becoming more open, especially on social media. Celebrities are sharing their experiences as parents of children with special needs, helping to normalize these discussions and inspire others. This shift fosters understanding and empathy, creating a more inclusive environment for everyone.
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