Ashton Kutcher and Mila Kunis keep their personal life away from the cameras. But recently, they attended a basketball game and brought their children out in public for the first time. Looking at the couple’s son and daughter, people noticed something.
Ashton, 46, and Mila, 40, who have been married since 2015, attended the women’s basketball game between the Indiana Fever and the Los Angeles Sparks in Los Angeles. They brought along their 9-year-old daughter, Wyatt, and 7-year-old son, Dimitri.
The picture-perfect family appeared to be having a wonderful time, and their happiness quickly caught the attention of fans, who showered them with compliments and the majority of observers noted how the kids are the spitting image of their famous parents.
One observer noted, ’’their kids are a literal copy of them both,’’ while another wrote that they are a ’’mix of two gorgeous parents’’. A third fan remarked, ’’The boy looks like Mila and the girl has Ashton’s face.’’
This is a significant move, as Ashton and Mila are among those celebrities who strive to keep their personal lives private and shield their children from public attention. They do not share their children’s photos on social media or bring them to red carpet events. However, in one of their interviews, they touched on the topic of children and shared their approach to parenting.
They have no intentions of leaving their hard-earned money to their 2 children. Instead, they want to give it to people who truly need it. Kutcher added, “I’m not setting up a trust for them. We’ll end up giving our money away to charity and to various things.”
Mila and Ashton have a combined net worth of around $250 million.
Another celebrity offspring recently caused a stir as well. Richard Gere’s 24-year-old son made his debut at Cannes, and everyone unanimously agreed that he is even more handsome than his father.
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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