People have cringed at footage of Demi Moore kissing a 15-year-old boy.
Resurfaced on social media, the event features the 19-year-old actress from Indecent Proposal attending her co-star Philip Tanzini’s 15th birthday party from General Hospital.
In the enduring American soap opera, Moore portrayed Jackie Templeton from 1982 to 1984, and Tanzini, Jeremy Hewitt, from 1979 to 1982.
According to the MailOnline, the video was purportedly shot in 1982 and first broadcast on Entertainment Tonight.
Since its January 2012 upload on YouTube, it has racked up an incredible 8.7 million views.
Throughout the evening, Moore can be seen kissing Tanzini three times throughout the entire clip.
Moore, who at the time was married to Freddy Moore, is heard in the tape praising her co-star and calling him one of her “favorite people.”
“I love Philip, and he’s the only one I love,” she declares. He is one of my most favorite persons, and I adore him so much.I adore him and he’s very wonderful.
“We’re going to get married, by the way. Don’t let her husband find out,” Tanzini continues.
Then Moore yells, “I can’t wait.”
People have been calling the footage “weird” and “disturbing” on social media since it was discovered.
“This kiss wasn’t a quick peck on the cheek or even the lips,” wrote one observer. Nor was it an isolated incident.Furthermore, I could really care less that it came from a woman—especially Demi Moore. It’s unsettling, or at the very least quite uneasy.
Another commenter said, “There’s still something a little strange about this. This fifteen-year-old appears much younger. Who knows, though?
“Of course, young men dream about older women—even me at that age—but that doesn’t change the fact that it’s an adult kissing a child.”Those aren’t just fast kisses; those are genuine kisses. Too strange. Always ask questions.
A third added their thoughts, saying, “I thought that kiss was way too long and intimate.” made me feel uneasy.
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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