“I can’t believe that tomorrow is our last show together,” said Vanna, 67. “I don’t know how to put into words what these past 41 years have meant to me, but I’m going to try. Eight thousand episodes went by like that.”
The duo has been hosting America’s Game since 1982 when the show first aired in syndication. Throughout the years, they became one of television’s most iconic duos, capturing the hearts of millions of viewers.
“As the years have gone by, we’ve grown up on television, but we’ve also shared so much more behind the scenes,” reminisced Vanna, reflecting on the personal memories they’ve shared. “What an incredible and unforgettable journey we’ve had. And I’ve enjoyed every minute of it with you.”
With tears welling in her eyes, Vanna held back her emotions and continued, “You’re like a brother to me, and I consider you a true lifelong friend, who I will always adore. I love you, Pat.”
After the segment, Pat and Vanna embraced in a heartfelt hug on stage, symbolizing the bond they have built over the years.
Throughout their partnership, Pat led the contestants through the game, while Vanna became famous for gracefully turning the letters on the puzzle board. Together, they have appeared in over 8,000 episodes, creating countless unforgettable moments for fans around the world.
“She’s a real Thumbelina” – Meet the girl who’s only 99cm tall and defied all the odds
Kenadie Jourdin-Bromley, a Canadian child from Ontario, seemed ordinary at first glance.
She had high hopes for the future, loved sports and drawing, and went to school.
Nonetheless, one characteristic set Kenadie apart from her peers: her diminutive height of 99 centimeters.
Reports state that when Kenadie was born in February 2023, she weighed a mere 2.5 pounds. Her condition was quickly diagnosed by doctors as an uncommon form of cardiovascular disease, thought to affect only 100 people globally. The nurses dubbed her “Thumbelina,” quite fittingly.
Regretfully, Kenadie had slim chances of surviving.
According to reports, the girl’s condition can lead to complications like delayed mental development, respiratory issues, and digestive issues. Doctors at the hospital where the girl was born were concerned that she wouldn’t have much time to live due to her brain injuries.
Understandably, her parents were devastated. In order to give their little girl a name in case she passed away, they chose to christen her on the day of her birth.
“We thought we were going to take her home to die, because that’s what the doctors told us,” mom Brianne explained to Barcroft TV back in 2016.
Still, as the days went by, Kenadie steadfastly refused to give up. After she triumphed over all the challenges and hardships, her parents were able to dream again that she would survive. It was nothing less than a miracle for them.
Many years later, Kenadie still astounds everyone she encounters. She is only 99 centimeters tall, her arms and legs are still immature, and she struggles to learn new things, but she is a content young girl who enjoys life to the fullest.
Kenadie reportedly enjoys bowling and ice skating. Above all, she makes people happy that she meets.
“Kenadie makes me laugh. She’s very empathetic – if you hurt your finger she comes and gives you a hug. She’s got an infectious laugh that makes you want to laugh along with her,” Kenadie’s assistant Jessica Putnam mentioned to Barcroft TV in 2016.
Naturally, Kenadie and her family face many new challenges in their lives. Despite her loved ones’ best efforts to take each day as it comes, the young girl is continuously dealing with medical issues.
“My hope for Kenadie’s future– my biggest hope for her– is I want her to be happy. I want her to smile and be successful. If we can get through today, then we’ll see about tomorrow,” her mom said.
We are happy to share Kenadie’s inspiring story!
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