After four miscarriages and plenty of plain to overcome, Paige and her husband, Victor, finally welcomed a child in their life.
The two were a great couple who knew what worked for them and what didn’t. After every miscarriage, Victor assured Paige that everything would be all right eventually, and that if they couldn’t have a baby of their own, they could always consider other options. His words were always comforting.
When baby Mason was welcomed into the world, it felt like all those shattered dreams had finally pieced themselves together. He became the center of his parents’ lives and they put him above everything else, including their careers.
Being a chief executive with a clothing brand, Paige needed to travel a lot because she was involved in every step of the product designs.
This didn’t bother her much because she knew Victor was a wonderful father who took great care of their child whenever she was away from home.
When Mason turned four, Paige knew he was about to enter pre-school soon so she decided to limit her work trips in order to be able to spend more time with him.
One time, Paige was away from home for three days, and once her work was done, she was eager to get home to her family and give her son a hug. Little did she know that this time would be different.
As she entered, the house was strangely quiet, with faint shuffling noises coming from upstairs.
Victor’s voice was hushed but urgent — the same urgency that Mason associated with misbehavior and bedtime.
“Buddy, you’ve got to promise me one thing, okay?” Victor said.
“Okay,” Mason muttered innocently. “What is it?”
“You’ve got to promise me that you won’t tell Mom what you saw.”
“But I don’t like secrets,” Mason said. “Why can’t I tell Mommy?”
Victor let out a deep sigh — its echo seemed to ripple through the house, as if carried by the air.
“It’s not a secret, Mason,” he said. “But if we tell Mommy, it’s going to make her sad. Do you want Mommy to be sad, buddy?”
“No, I don’t,” Mason answered.
At that moment, pretending she didn’t hear a thing, Paige yelled, “Mason! Victor! Mom’s home!”
“What’s going on?” she asked, as Mason leaped into her arms.
“Nothing, honey,” Victor said, winking. “Just a boys’ chat. Welcome home.”
Since Victor was the perfect husband and father, Paige tried to convince herself that the conversation she overheard was truly nothing important. She thought to herself that Victor probably gave Mason too many sweets or let him eat junk food, and that’s what they tried to hide from her.
However, letting it go seemed harder that she thought.
The week that followed and the trip she had to take were both a blessing and a curse for Paige. As much as she loved her job, the thought of leaving Mason saddened her profoundly. She only found solace in the photos Victor sent her, and one of those photos brought more questions than answers.
In one of the photos showing Mason playing with his toys, Paige spotted blue shows she had never seen before. They weren’t hers, yet they were there in her living room.
Paige decided to scroll through each of the photos Victor has ever sent her, and she did find more evidence of someone being in their home while she was away. Was it a nanny he hired to take care of their son? If yes, she had a very expensive taste.
This time, Paige decided to return home without telling Victor. She wanted to surprise him.
Once home from her trip, she entered straight to Mason’s room who had just woken up and was rubbing his eyes.
“Dad’s not downstairs?” she asked, as she could hear noises coming from the bedroom. “Mommy, don’t go in there. You’ll be sad,” Mason warned her.
In the bedroom, Victor was in bed with another woman. “Paige!” he exclaimed, sitting up in bed. “It’s not what you think!”
“Do I look that stupid?”
The woman took her clothes and entered the bathroom, locking the door behind her.
The ensuing confrontation was a whirlwind of tears, accusations, and heartbreak. Victor attempted to deny everything, relying on his charm. Paige knew that if she hadn’t seen it with her own eyes, she might have fallen for his lies.
“I have nothing else to say to you,” Paige said.
“What did you expect, Paige?” Victor asked.
The woman fled the house and Paige was left to confront the man she no longer knew.
“You’re never here,” he lashed out. “You’re never around. And when you’re home, you spend all your time on Mason or working. What about me?”
He tried to portray himself as a victim. “I need human contact, too,” he said. “And I don’t know what you get up to when you’re flying all over the country. I bet you’ve got stories, too.”
“No, Victor,” she said. “I’m not you. My vows meant something to me.”
Eventually, Paige asked Victor to move out and filed for divorce. Reflecting on that conversation between him and Mason that she had overheard, Paige realized the signs were always there, but she tried to ignore them because she only saw the good in her soon to be ex-husband.
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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