“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
The Iconic Blonde Beauty from ’10’ at 67: Here’s How Bo Derek Looks Today
Bo Derek was raised in a middle-class family after being born in Long Beach, California, on November 20, 1956, under the original name Mary Cathleen Collins. Her mother, Norma Bass, was a hairstylist and cosmetics artist, while her father, Paul Collins, was a public relations executive.
Bo’s early professional interests in the entertainment sector were influenced by her parents’ jobs.
When she met John Derek, an actor and director thirty years her senior, in her late teens, her road to stardom officially began. After John divorced actress Linda Evans in 1976, they started dating. Bo’s career was significantly shaped by John.
Bo made her big screen debut in Blake Edwards’ 1979 film “10,” in which she portrayed Jenny Hanley. She became an immediate sex icon and gained international recognition after the iconic video of her sprinting on the beach in a nude one-piece swimsuit went viral.
Career in Acting
Following the popularity of “10,” Bo Derek acted in a number of films directed by her husband, John Derek, in the 1980s, including “Tarzan, the Ape Man” (1981), “Bolero” (1984), and “Ghosts Can’t Do It” (1989). Even if a few of these movies were financially successful, critics frequently gave them negative reviews. Still, Bo remained a symbol of his era’s culture.
Life Apart from Performance
Bo Derek turned her attention to other pursuits after her film career faltered. She joined the California Horse Racing Board and started advocating for animal welfare. She has also actively participated in numerous humanitarian endeavors and supported causes related to veterans.
Bo shared details about her life and profession in her book, “Riding Lessons: Everything That Matters in Life I Learned from Horses,” which was published in 2002.
John Derek and Bo were wed till his passing in 1998. Their relationship, which was characterized by a large age gap and professional cooperation, was often featured in the media.
Following John’s passing, Bo befriended actor John Corbett, who was well-known for his parts in the television series “Sex and the City” and “Northern Exposure.” The pair has been dating since 2002 and has kept their personal lives mostly to themselves.
Her legacy has been further solidified beyond her acting career by her philanthropic work and advocacy for animal welfare.
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