“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
Blake Lively’s Daughters Make Rare Public Appearance — People Are Noticing the Same Thing
Blake Lively and Ryan Reynolds’ daughters stole the show at a concert. Fans couldn’t stop talking about a detail they noticed about the girls, who rarely appear in public with their mom.
Blake Lively and Ryan Reynolds’ daughters made a rare public appearance, joining their mother at Taylor Swift’s Eras Tour show in Madrid on May 29. Videos shared on social media captured the family enjoying the concert from the VIP section, where fans couldn’t help but notice the girls’ striking resemblance to their famous mother.
Lively went for a laid-back but trendy vibe during the outing, sporting a neat white button-up shirt paired with denim shorts and stylish gold hoop earrings. Her blonde hair was styled in a loose, pretty down-do, adorned with clips that added a touch of flair with a side part.
The mother and daughters appeared to be thoroughly enjoying the performance, engaging in socializing and exchanging bracelets. Videos capturing their outing have been widely circulated on social media platforms.
However, fans were quick to notice the strong resemblance between Lively and her daughters, flooding social media with comments. Admirers gushed over the girls, saying things like, “They have their momma’s face. So cute,” “Blake with her minis,” or “Blake’s babies look like their mama, and I’m sure they’re kind too!!” someone else wrote.
On the contrary, another fan noticed a resemblance to her husband, writing, “They look so much like Ryan.”
Now, people are buzzing with speculation about whether Swift has revealed the name of Lively and Reynolds’ fourth child in her latest album. This is because Swift often includes their kids’ names in her songs.
Reynolds humorously addressed the speculation, saying, “We always wait for Taylor to tell us what the child’s name will be.”
Blake Lively’s public outings and interactions offer a peek into their family life.
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