For nearly two decades most of us can remember tuning in to see the latest adventures of the most famous dog on TV – Lassie.
This much-loved Rough Collie dog and her human companions graced our screens for 17 seasons from 1954 to 1973 and even made the transition from black and white to color in the ’60s.
But who could forget the adorable little boy who joined the show in its fourth season when he and his family adopted Lassie – 7-year-old Timmy Martin.
Now Jon Provost, who played Timmy, has celebrated his 74th birthday and shares the joy he had filming with his four-legged friend and how he was discovered by Hollywood at just 3 years old.
The Los Angeles-born actor said when he was 3 years old he was taken to an audition for a Jane Wyman movie because his mom was a huge fan and hoped to get her autograph. But, out of the 200 kids auditioning for the part, Jon got it.
It was far from evident that Jon would become an actor. His father worked with something completely different – he was an aeronautical engineer.
”My parents weren’t Hollywood people. My father is from Alabama and my mother is from Texas,” Jon said.
At age 4, he landed a role in a Grace Kelly and Bing Crosby movie.
“I didn’t have an agent. I got one and that led to more movies like The Country Girl with Bing Crosby and Grace Kelly. I did about 12 movies before I started ‘Lassie’”, he told Fox News.
Three different Lassies
Recalling the bonds he formed with the three different male dogs that played the part of the female Lassie, Jon said he developed the biggest bond with the last dog to play Lassie.
“I did the show for seven years, 249 half-hour episodes. I worked with three different Lassies. The last dog I worked with, I worked with him for five years alone,” he told Fox News.
“We grew up together. For five years, we saw each other five days a week and sometimes on weekends.
Revealing how well behaved the dog was he added: “The actors made more mistakes than the dog. They were more of a problem,” he laughed.
After leaving the show at 14 years old he starred alongside the likes of Natalie Wood and Kurt Russell and never fell into the Hollywood child actor trap saying: “My parents let me pretty much do what I wanted to do. I didn’t have to take a job.
“When I left Hollywood, I thought it was good that I did.”
Today Jon lives out of the limelight in Northern California but still gets fan mail from his time in “Lassie”. In 1994, the actor received a star on the Hollywood Walk of Fame.
Meanwhile, Lassie, the canine character, became so popular that she even had a “Lassie” riveting radio series.
Jon Provost wife
In 1979, Jon Provost tied the knot with Sandy Goosens. Together, they had two children, Ryan and Katie.
After being married for 14 years, the two divorced on December 20, 1993.
In 1999, Jon Provost found love again when he married Laurie Jacobson, a well-known researcher, and author.
I was such a fan of the adventures this sweet duo got up to. And with a moral to every episode, it was the perfect show for kids.
Please share with all the “Lassie” fans you know.
A Man Who Was Called “The Tree Man” Was Able to Hold His Daughter Again After Many Surgeries
“The Tree Man” is a man whose life has been defined by a rare malformation in his hands. Once dubbed for his distinctive condition, he has undergone numerous surgeries, overcoming tremendous challenges on his journey. Now, with unwavering determination and the skilled hands of medical professionals, he has reclaimed a simple yet profound joy—holding his daughter once again.
Abul Bajandar has a rare condition called ’Tree Man’ Syndrome.
Abul Bajandar, a man hailing from Bangladesh, is afflicted with an extraordinary and rare condition known as ’Tree Man’ Syndrome. This hereditary condition, though non-contagious, is unfortunately incurable, and surgical interventions offer only temporary relief. Abul is not alone in his struggle, as there are others worldwide grappling with the challenges posed by this syndrome.
This syndrome manifests through the development of wart-like skin growths that bear a striking resemblance to tree bark. These growths, while initially small, have the potential to grow significantly in size, resulting in considerable disability for those affected.
He has it from a young age.
The onset of his condition began during adolescence, with small warts appearing on his body at the age of 13-14. Regrettably, as he advanced in age, the affliction rapidly escalated, affecting various parts of his body.
After 16 surgeries he was able to hold his daughter again.
After undergoing a series of 16 surgeries between 2016 and 2017 at Dhaka Medical College Hospital in Dhaka, Bangladesh, Abul Bajandar achieved a poignant milestone—he could once again hold his daughter. The surgical procedures aimed to remove the bark-like lesions from his hands and feet, offering a glimmer of hope in his battle against Tree Man Syndrome.
Bajandar shared the profound joy he experiences spending time with his daughters, emphasizing, “If I recover from this, I want to work again, to build a small business to help my daughters in her studies and to give them a good life.” These words reflect not only his determination to overcome the challenges posed by his rare condition but also his unwavering commitment to providing a better future for his family.
Throughout Abul Bajandar’s challenging journey with Tree Man Syndrome, he draws strength from the unwavering support of his wife and mother. In the face of the condition’s recurrence, their steadfast presence provides him with comfort and encouragement. Bajandar reflects on the transformative power of fatherhood, sharing, “When my daughter was born, she brought me the hope of life again. I didn’t want to leave her as an orphan. I felt like I must live for her.”
Abul Bajandar’s condition returned but he remains hopeful.
Despite facing the disheartening recurrence of his condition, Abul Bajandar maintains a resilient sense of hope. Doctors, initially uncertain about the possibility of the condition’s return, witnessed its reappearance. Undeterred, Bajandar expresses his unwavering optimism, declaring, “My only dream is to recover from this situation and live a healthy life.”
His poignant words reflect not only the personal challenges he endures but also a universal desire for health and well-being. Bajandar’s enduring hope shines through as he states, “All I can say is that I truly believe and hope that a cure exists for this disease.” In the face of adversity, his spirit remains unbroken, embodying the strength of individuals confronting rare and challenging medical conditions.
Another person born with a rare condition has defied societal norms and emerged as a symbol of extraordinary resilience. Meet the girl affectionately referred to as “Voldemort” due to being born without a nose.
Preview photo credit Tansh / Alamy Stock Photo, ZUMA Press, Inc. / Alamy Stock Photo
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