“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
His charm and good looks made all the ladies drool. Now he is 94, this is how he looks today
Robert Wagner was born on February 10, 1930, in Detroit, Michigan. His family moved to Los Angeles when he was seven, which set the stage for his future career in Hollywood.
Wagner developed an early interest in acting and landed his first film role in “The Happy Years” (1950) after being discovered by a talent scout.
Hollywood Success
Robert Wagner’s career took off in the 1950s, with significant roles in films like “With a Song in My Heart” (1952) and “Titanic” (1953). His charm and good looks made him a popular leading man. Throughout the 1960s and 1970s, he continued to build his reputation with roles in movies such as “Harper” (1966) and “The Pink Panther” (1963).
Television Stardom
Wagner is perhaps best known for his extensive television career. He starred in several successful TV series, including “It Takes a Thief” (1968-1970), where he played the suave thief-turned-spy Alexander Mundy.
In the 1970s, he found further success with “Switch” (1975-1978) and “Hart to Hart” (1979-1984), where he played the charming and wealthy Jonathan Hart, alongside Stefanie Powers. These roles solidified his status as a television icon.
Personal Life
Robert Wagner’s personal life has been as intriguing as his career. He was married three times, twice to actress Natalie Wood, whose tragic death in 1981 remains a topic of public fascination.
In 1990, he married actress Jill St. John, and the couple has been together ever since. Wagner’s enduring marriage to St. John and their frequent collaborations highlight their strong personal and professional bond.
Later Career and Legacy
In the later years of his career, Wagner continued to work in television and film, making memorable appearances in shows like “Two and a Half Men” and “NCIS.” He also wrote his autobiography, “Pieces of My Heart,” published in 2008, offering insights into his life and career.
Robert Wagner’s contribution to the entertainment industry spans over six decades, making him a beloved and enduring figure in Hollywood. His versatility and charm have left an indelible mark on both film and television, ensuring his legacy will be remembered for generations to come.
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