“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
My Parents Forbade Me from Moving Out — When I Discovered Their Real Reason, I Immediately Called the Police
Taylor’s excitement about moving into her dream apartment was shattered by a devastating betrayal. Her parents had secretly taken out a loan in her name, using her savings without her knowledge. Faced with this painful truth, she made a bold decision that changed her family’s future forever.
My name is Taylor, and I want to share a story that turned my life upside down. I never thought I’d experience such betrayal, let alone talk about it. But here I am.
I recently finished my third year of university and stumbled upon the cutest little apartment near campus. It had everything I ever wanted: huge windows, a cozy reading nook, and a charm that felt like home. I was over the moon and couldn’t wait to tell my parents.
One sunny afternoon, I sat down with them in our living room, unable to contain my excitement.
“Mom, Dad, guess what?”
I looked at him, tears filling my eyes. “I hope so. It just feels like everything is falling apart.”
“Maybe,” he said softly. “But sometimes things need to fall apart to fall back into place. This is a lot to handle, but you have me and Aunt Freya supporting you every step of the way.”
Aunt Freya nodded. “Jake is right. We’re here for you, Taylor. And you’re stronger than you think. Never forget that.”
The legal process was long and stressful, but eventually, justice was served. My parents were held accountable for their actions, and I felt a sense of closure.
Do I feel bad for them? Sometimes. They were my parents, after all. But I couldn’t let them ruin my future. I had to take a stand, even if it meant breaking the family apart.
They looked up from their newspapers, giving me a curious glance.
With the support of Aunt Freya and Jake, I slowly started to rebuild my life. I found a new job, saved up again, and eventually moved into my dream apartment. It wasn’t easy, but I knew I had made the right choice.
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