“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
I Found My Daughter Sleeping Under the Stairs—Her Chilling Confession Left Me Shaken
In-laws are supposed to make life easier, right? Well, not in my case. This is the story of how I got back at Linda, who thought she could treat my eldest daughter, Tessa, badly and get away with it.
I have two daughters. Tessa, who is 10, is from my first marriage. She’s sweet, quiet, and always tries to make everyone happy. My younger daughter, Sadie, is 4, from my marriage to Grant, my current husband. Sadie is the opposite—full of energy and always asking questions. Grant loves both girls, but his mother, Linda, feels differently, especially toward Tessa.
Linda is the type of person who wants everything to appear perfect on the outside. But underneath, she’s judgmental and cold, particularly when it comes to Tessa. The reason? Tessa isn’t Grant’s biological daughter.
For years, I tried to keep the peace. Grant would say, “She’s just old-fashioned,” but it was clear Linda’s behavior wasn’t fair to Tessa.
“She’ll come around,” Grant would say. But Linda never did. Instead, she made small, hurtful comments toward Tessa.
Tessa, bless her, never complained. She stayed quiet, probably thinking it was her fault. But I noticed everything. I heard the comments, and each time, it made me angry.
Grant? He didn’t see it the same way. He loved his mom and thought she was just being her usual, quirky self.
I always thought in-laws were supposed to make life easier. But not in my case. This is the story of how I got revenge on Linda, my mother-in-law, who treated my eldest daughter, Tessa, like she didn’t matter.
I have two daughters. Tessa, 10, is from my first marriage. She’s sweet, quiet, and always tries to make people happy. Sadie, 4, is from my marriage to Grant, and she’s full of energy. Grant loves both girls, but his mother, Linda, acts differently, especially toward Tessa.
Linda often made rude comments about Tessa. Sometimes, she’d say things like, “Oh, Tessa, that dress is a bit too grown-up for you, don’t you think?” She would forget Tessa’s birthday but spoil Sadie with gifts.
Things got worse after my own mother passed away. I was crushed by grief, barely able to function. We had to travel out of state for the funeral, and Linda offered to watch the girls. I didn’t want to leave Tessa with her, knowing how uncomfortable she’d be, but I had no other choice.
Three days later, we returned home, and the house was eerily quiet. Linda left a note saying she had taken Sadie to the park, but I couldn’t find Tessa. My heart raced as I searched the house. Then, I saw a light coming from the basement. I went downstairs and found Tessa, curled up on the cold floor, sleeping under a blanket, with dried tears on her face.
“Tessa, why are you down here?” I asked, heartbroken. She told me Linda had made her sleep there, saying Sadie was her “real” granddaughter and they needed “special time” together.
I was furious but knew confronting Linda wouldn’t change things. Instead, I decided to get even. Linda’s family reunion was coming up, and it was her pride and joy. I offered to help her organize it, pretending everything was fine. But behind the scenes, I was telling the family how Tessa was treated, especially during the funeral.
At the reunion, I put together a slideshow of family photos. But in the middle of all the happy pictures, I included a clip of Tessa sleeping on the basement floor. The mood shifted immediately. People were shocked, whispering, “Why would she be down there?”
Linda’s perfect image crumbled as the family questioned her. She tried to explain, but it was too late—everyone saw her for who she truly was. I didn’t need to say anything; the photos said it all.
Since that day, Linda hasn’t spoken to me, and honestly, that’s just fine with me. I’ll always protect my daughter, no matter what.
Leave a Reply