“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
Princess of Monaco Grace Kelly’s granddaughter is all grown up and has inherited her grandmother’s beauty
Grace Kelly was a Hollywood film star who never left the spotlight in the 1950s. She didn’t last longer than six years in the industry, but those years she spent were legendary.
She got into the world of acting at the age of 20 and became a bomb.
She starred in adventure romance Mogambo alongside Clark Gable and Ava Gardner which earned her a Golden Globe for best-supporting actress.
We thought that was all until she gave a show the following year. She won yet another award for Best supporting actress in The Country Girl.
During her career, her movies were majorly comedy musical High Society starring alongside Bing Crosby and Frank Sinatra and three Alfred Hitchcock movies Dial M for Murder; To Catch a Thief with Cary Grant, and Rear window.
At the age of 26, Grace left the spotlight because of her marriage to Prince Rainier III and become Princess of Monaco.
We all knew if she remained in the industry she could have been among the top as within six years she had two Golden Globes and Academy Award to her name and 11 successful movies.
She retired from the spotlight because of her marriage to the prince and went on to have three wonderful children, Caroline, Princess of Hanover, Albert II.
Kelly tragically passed away at the age of 52 after a car accident. She had a stroke and lost control of the vehicle. Stephanie, her youngest daughter was with her at that moment, and luckily she was able to survive the accident.
Kelly is said to have a total of 11 grandchildren and they so much remind us of the Philadelphia-born.
Camille Gottlieb is one of the grandchildren of Kelly born by Grace Kelly’s youngest child Princess Stephanie of Monaco and Jean-Raymond Gottlieb.
The 20-year-old has two older half-siblings, Pauline Ducruet and they look so much like their grandmother.
Camille seems to be a better replica of her grandmother as she has blond hair and blue eyes.
Going through her Instagram account with over 70,000 followers, we can’t help but see her grandmother’s piercing blue eyes. She looks so beautiful and reminds us of the legendary Grace Kelly. May her soul rest in peace.
The report says she’s not quite eligible for the throne as she was born when her parents weren’t married and her birth was a secret.
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