Emily
An individual known as “The Tree Man” has faced a life marked by an unusual hand malformation. Initially acknowledged for this distinctive condition, he has undergone multiple surgeries, triumphing over substantial challenges. Presently, driven by unwavering determination and the skills of medical experts, he has rediscovered a simple yet profound joy — the ability to embrace his daughter once again.
Abul Bajandar suffers from a rare condition identified as ‘Tree Man’ Syndrome.
A Bangladeshi resident named Abul Bajandar is confronting an extraordinary and rare condition known as ‘Tree Man’ Syndrome. Despite being non-contagious and hereditary, the syndrome, unfortunately, lacks a cure, with surgical interventions offering only temporary relief. Abul is not alone in this struggle, as individuals worldwide grapple with the challenges presented by this syndrome.
Characterized by wart-like skin growths resembling tree bark, the syndrome initially begins as small formations but can progress significantly, causing considerable disability for those affected.
He has had it since he was young.
Abul Bajandar first experienced the onset of his condition during adolescence, noticing the emergence of small warts on his body around the age of 13-14. Regrettably, as he grew older, the affliction quickly escalated, affecting various parts of his body.
Following 16 surgical procedures, he was able to embrace his daughter once more.
Having undergone a sequence of 16 surgeries between 2016 and 2017 at Dhaka Medical College Hospital in Bangladesh, Abul Bajandar achieved a noteworthy milestone — the ability to embrace his daughter once more. The surgeries were intended to remove the bark-like lesions from his hands and feet, offering a promising development in his battle against Tree Man Syndrome.
Bajandar expressed the immense joy he feels while spending time with his daughters, underscoring, “In the event of my recovery, I aspire to resume work and establish a small business to support my daughters’ education and ensure they lead a good life.” These sentiments not only convey his resolve to surmount the obstacles presented by his uncommon condition but also illustrate his steadfast dedication to securing a brighter future for his family.
In the midst of Abul Bajandar’s challenging battle with Tree Man Syndrome, he draws strength from the steadfast support of his wife and mother. Faced with the recurring challenges posed by the condition, their unwavering presence serves as a comforting and motivating force. Contemplating the profound influence of fatherhood, Bajandar articulates, “When my daughter was born, she brought back the hope of life for me. I couldn’t bear the thought of leaving her as an orphan. I felt a strong determination to live for her.
Despite the Return of Abul Bajandar’s Condition, Hope Persists.
Despite facing the disheartening resurgence of his condition, Abul Bajandar stands resilient and optimistic. Initially uncertain about the possibility of its return, doctors have confirmed its reappearance. Undaunted, Bajandar maintains unwavering hope, stating, “My sole dream is to recover from this situation and lead a healthy life.”
His poignant words resonate not only with the personal hurdles he confronts but also echo a universal yearning for health and well-being. Bajandar’s enduring optimism shines through as he affirms, “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, exemplifying the strength of individuals grappling with rare and formidable medical conditions.
Yet another person, born with a unique condition, has defied societal expectations and emerged as a symbol of exceptional resilience. Let us acquaint you with the girl affectionately known as “Voldemort” due to her being born without a nose.
