A father worried about why his daughter often remained behind in the school bus after others left, so he decided to find answers. What he found was not what he expected.
Benjamin Bruce was a single dad who had to step in to become his child’s mother after she passed away. Their daughter, Emily, had been six when it happened.
Ben loved his daughter because, to him, she was all that was left of his beloved wife, and he had also promised her that Emily would be well taken care of no matter what.
To that end, Ben tried his best to juggle work while being present in his daughter’s life. He had no other family he trusted to look after her, so he had to do everything himself.
The first couple of years were rough on him as a parent, and just as he was acclimatizing to the rollercoaster, his daughter hit puberty, and at that point, things got wilder.
She suddenly started going through physical changes right before his eyes, and he knew what they meant — the boys would be coming for her. How could they not; his daughter had his late wife’s red hair and deep green eyes that seemed designed to mesmerize.
Even Ben was not immune to her eyes and had fallen prey to her will multiple times over the years. When she clocked 12, two years after she hit puberty, Emily discovered boys.
That led to her paying a lot of attention to her hair and appearance because she wanted to look good for her school crush. Ben was prepared to beat back boys with a stick if need be, but what he was not ready for was caring for his daughter’s looks.
Emily had to do that herself, but she was terrible at it with no role model to learn from. Ben often just cut her hair short as a child because he knew nothing about hair care, but he had to respect her wishes to keep her hair longer as she grew older.
There was little he would not do for his child, so to help her, he started brushing her hair when it was long enough. He was a big man, and even though he tried to be gentle, he occasionally pulled it out.
“Ouch!!!!” she yelled one day.
“I’m sorry baby,” he apologized quickly, as he always did.
“You need to be more gentle daddy,” she would admonish him sometimes.
Other times, she just endured the pain because she did not want to make her father feel terrible for causing it. Ben felt the sting of his failure each time his daughter complained of her hair getting pulled out, and that made him try to cut her hair again.
“Just get rid of it all,” he would say when they argued about it sometimes. “Your mom kept her hair cropped short and she still looked wonderful.”
“Daddy, I will no longer cut my hair, look how slow its growth is because of how often you cut it in the past,” she would shoot back. In any case, Ben never won the arguments, but he didn’t need to; they stopped coming up after a short while.
Shortly after that, he noticed that his daughter started getting tardy notices from her class teacher, Mrs. Flynn. So he called the woman to find out.
“That’s right, Mr. Bruce. Your daughter has five tardy notices this week alone. Is there anything going on I should know about?” the woman asked him.
“Nothing is going on. Things have been great at home for some time now and I do release her to join the bus early so I’m sure she makes it to school when others do,” he explained.
“Did you notice anything going on with her this past week?” Ben asked.
“Well, I was running late for class once and I saw her alight from the bus rather late even though she should have been in class by that time. The driver probably knows something about it because only they can access the bus at any time.”
“Thank you, Mrs. Flynn, I’ll get to the bottom of this,” Ben told her before ending the call.
Worried about why his daughter was spending extra time on a bus, Ben followed her the next day. True to what Mrs. Flynn told him, he noticed that everyone on the bus alighted when it arrived on the school grounds — everyone but his daughter.
As soon as he could, Ben burst into the bus in a rush thinking the worst but was instead met with the scene of a nice 40-year-old woman combing his daughter’s hair. The woman, Madeline, was the bus driver.
“Mr. Bruce?” the woman exclaimed at his sudden entry as Emily looked up, surprised to see her father.
“Dad? What are you doing here?”
“Hello ma’am,” Ben said after clearing his throat and righting himself. “Sorry about barging in, but I heard my daughter was getting tardy notices so I came to see why.”
“Oh, well in that case, here’s why,” the woman said, gesturing to his daughter’s hair. “I noticed how she seemed to struggle with her hair so I offered to help her brush it every day before she goes to class because she says her rough hair often makes her feel bad.”
“Honey,” Ben said to his daughter. “You never told me this.”
“I just didn’t want you to worry about it,” Emily defended.
Later that day, Ben invited Madeline for coffee. When the bus driver heard about what happened to his wife, she started to cry.
She herself was a cancer survivor, and she was well aware of how lucky she was to have pulled through and was grateful that she could still be there for her own children.
Madeline was convinced she survived for the kids on the bus who needed somebody to talk to or do their hair or whatever, so she begged Ben to find a compromise that would help his daughter.
To that end, Ben spoke to Mrs. Flynn, her teacher, and after explaining things to the woman, Emily was never given a tardy notice again. Ben was grateful to Madeline, and he remained close friends with her for a long time.
What did we learn from this story?
Never jump to conclusions. Ben gave himself a fright when he immediately assumed something sinful was happening between the bus driver and his child, and if he had not taken the pains to confirm it, things might have taken a terrible turn.
Give back when you can. Madeline believed he was spared from death to take care of other kids, and that was what she did. Caring for those kids was her way of giving back, and it left her feeling fulfilled, especially since she was able to touch lives like Emily’s and Ben’s.
Share this story with your friends. It might brighten their day and inspire them.
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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