“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
Playground craze leaves 11-year-old boy “looking like an alien” – mom issues warning for parents
no to something that sounds dangerous.
Unfortunately, children are susceptive to peer pressure and the like; even the most intelligent of youngsters can be coerced andfmconvinced to partake in stunts that promise dire consequences.
Just ask the parents of 11-year-old Tyler Broome, who suffered horrific injuries after trying a YouTube craze known as ‘the roundabout of death’.
Yes, the name alone pretty much tells you the salient facts of the matter, but for Tyler it wasn’t so much an incredibly dangerous stunt as a way to show his friends how fearless he was.
The 11-year-old thereafter sustained injuries consistent with those seen in fighter pilots, after bein subjected to extreme gravitational force (G-force).
The craze he participated in – known as the ’roundabout of death’ – sees participants sitting in the middle of a playground roundabout whilst it’s spun at high speed using the rear wheel of a motorcycle.
Shortly after the ordeal, Tyler was found unconscious near the roundabout, left with possible damage to his brain and vision.
Extreme force
It’s believed he was subjected to the sort of G-force usually only encountered by pilots and astronauts.
It’s reported that Tyler was at a local park with a friend when they were approached by a group of older teenagers who dared them into the game.
Terrifying ordeal
“I don’t recognise my child – he is on the verge of having a stroke. Tyler sat on the roundabout, and the boy who came over was about 17. Tyler doesn’t know him, they are not friends,” his mom Dawn said, per British newspaper The Independent.
“He puts his motorbike on the floor, gets the roundabout spinning at such a speed. When they all stopped, the group just cleared off – it is bullying.”
Dawn claimed that hospital staff had never seen such injuries and had to do research before they were able to begin treating her son.
“The injuries were so extreme, he just looked like the Elephant Man. They have never seen it before, they are going to make a medical report from it.
“His head has completely swelled up, his blood vessels have burst, his eyes look alien. His vision is blurry. You can manage a broken arm but this? He doesn’t remember it, he doesn’t remember the detail.”
Parents, please always bear in mind that children are susceptible to trying things we adults would stay well clear of.
Our thoughts and prayers go out to young Tyler and his family. Share this story to spread the warning over an incredibly dangerous game.
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