As a handsome carpenter, Ty Pennington rose to fame; nevertheless, he no longer looks the same. Regretfully, the 58-year-old celebrity has experienced criticism and bullying on social media. He has been dubbed “disgusting,” “fat,” and “gross” by others. Ty finally had enough, and his most recent response to the critics is outstanding.
Several people have fallen in love with Ty Pennington, the host of Extreme Makeover: Home Edition, ever since he made an appearance on the well-liked BBC show Trading Spaces, where he worked as a carpenter. Being incredibly talented and attractive, it was no surprise that Ty was asked to host one of the greatest programs for the underprivileged.
Ty was in the spotlight as the show’s host, but being on the set had its costs. He had a hard time finding time for himself.
“I went ten years without seeing my family or a partner. In 2019, he told The Atlanta Constitution, “I would go out again, come home, do laundry.”
“My God! People from the old TV show exclaimed when they saw me. You look fantastic! I slept for a while! I think my appearance has improved significantly from the time I was on the show.
To be honest, Ty wasn’t always interested in being a builder. Instead, he intended to become a graphic designer and worked in construction to help pay for art school. However, his modeling career was derailed by a near-fatal car accident, so he resorted to carpentry.
“My career appeared to take off overnight. Sadly, fate had other ideas. I would be in a terrible vehicle accident only a week later,” he posted on Instagram. “I put my one good headshot on display, grabbed my handy tool bag, and returned to carpentry and construction. I received an audition call for Trading Spaces nine years later, and the rest is history.
He first made his Hollywood debut as a set designer for Nicholas Cage’s 1995 picture Leaving Las Vegas, but it wasn’t until he appeared as a builder on Trading Spaces—the show that upended preconceived notions about home remodeling—that he became well-known.
Ty moved on to other endeavors when Extreme Makeover: Home Edition, which had won him two Prime Time Emmy Awards, was canceled back in 2011. He appeared on The Revolution, an ABC chat show, and then On The Menu and American Diner Revival, two cookery programs. In addition, he launched a design store in Los Angeles. In addition to participating in the third season of Deluxe Corporation’s Small Business Revolution: Main Street, Ty renovated Trading Spaces in 2018. He was seen hosting Battle on the Beach most recently.
He wasn’t asked to return to Extreme Makeover: Home Edition when the show recently aired again, but he insisted there are no ill will or ill blood.
Ty currently hosts the program Rock the Block and serves as a mentor and design consultant on HGTV’s Battle on the Beach.
In November 2021, Ty tied the knot with 33-year-old Kellee Merrell, a social media manager. He announced the wonderful news on Instagram by sharing a picture with the remark, “It’s the ‘yes’ for me,” and proposed to her with a stunning tea-drop-shaped diamond ring.
Although they have known each other for a long time, they didn’t begin dating until last year when they happened to cross paths.
“I’ve long admired Kellee from a distance. Ty told People, “She’s a beautiful person on the inside and out.”
Fortunately, the proper moment finally came for our paths to cross. It’s one of those situations where being with someone makes you feel content. She altered my perception of marriage, which I had never held. I’m happy I held out for the one.
After several viewers pointed out that he no longer had a six-pack, the host shared a humorous video of him from the beach last year with his shorts hiked up to his stomach. He also remarked that “he was pushing his stomach out.”
“What was an honest moment of just trying to make my wife laugh, was then picked apart by strangers- with a lot of views, comes a lot of hate!” he said in a lengthy Instagram post titled “Thoughts on Aging,” in response to the criticism. Remarks such as “gross,” “disgusting,” “grandpa,” “he got fat,” “omg he’s so old now,” etc.And I pondered whether I would receive the same remarks if I was still in good health. “Maybe we should extend the same grace to men as we do to women? There has been such a force behind accepting all shapes and sizes and aging in the female community, which is AWESOME (keep it coming),” he said.
Of course, he was much younger than he is now when he made his television debut.
“Every day, I get a ton of comments like, ‘NOOOo, what happened to him????’ The other day, I heard someone say, “lack of exercise,” which I hope was accurate! Seven days a week, I work out harder than I have ever worked out in my life (this over 50 sh*t is no joke). It’s been 22 years since my television debut, so here’s what occurred! He penned. “No, I don’t have a six pack or a gorgeous head of hair with frosted tips anymore, but at 57 years old, I’ve never been happier! I do, however, have wisdom, empathy, and life lessons! All of this is to indicate, nevertheless, that I am a human being with feelings. Yes, I am older, but that’s kind of cool, in my opinion.
In our opinion, he looks fantastic.
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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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