When we discovered a hidden room in our newly purchased home, we never imagined it would change our lives. What we found inside forced us to move out, but it also led to an unexpected twist.
I never thought I would experience anything like a horror movie, but here I was. After years of saving, Jack and I finally bought our first house. I was thrilled and eager to start renovations, taking charge while Jack focused on work.
One Tuesday morning, while sipping coffee and scrolling through my phone, Carlos, our renovation crew leader, called me over. He had discovered a hidden door behind a section of the wall they had just torn down.
Curiosity piqued, I opened the door, only to be hit with horror. Inside was a closet filled with old clothes, covered in mold and crawling with insects. The stench was overwhelming. Shocked, I quickly shut the door and called Jack to come home.
When Jack arrived, I led him to the hidden room. His reaction mirrored mine as he realized we couldn’t stay in a house with such a dark secret. We spent hours packing essentials and making arrangements to stay with friends, uncertain about what the future held for us.
Living at our friends’ place felt like we were back at square one. I worried about what would happen to our dream home, and Jack worked late, feeling guilty about the situation. Eventually, after several pest control visits, we received a call that changed everything.
The pest control team had found a wooden box while cleaning out the hidden room. Inside were vintage pieces of jewelry. Excited but confused, we wondered why the previous owner had left them behind. After researching, we decided to sell the jewelry and use the money for renovations, transforming our nightmare into something positive.
Selling the jewelry turned into an adventure of its own. We visited various shops, learning that some pieces were quite valuable. The sale brought in more money than we expected, allowing us to renovate the hidden room and upgrade the rest of the house.
Weeks later, the hidden room became a cozy reading nook, and the rest of the house transformed with modern appliances and a beautiful back porch. On the day we moved back in, I marveled at how different the space was. To celebrate, we hosted a housewarming party, and our friends were amazed by the renovations. Jack praised my efforts in turning things around, and I felt a wave of pride.
Later, as we relaxed in our new reading nook, Jack joked about being grateful for a room full of bugs. I laughed, realizing that our journey had led us to something even better than we had originally dreamed. In the end, I knew we could face any surprise together. Looking back, I just hoped our next renovation would avoid any hidden horrors.
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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