“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
Bruce Willis: A Remarkable Life
Fast forward to the present, and there’s a renewed interest in Bruce Willis’s career, specifically his iconic role in the 80s TV show “Moonlighting.” The show, also known as “Maddie & David,” has made a comeback on a streaming platform, thrilling fans worldwide. Glenn Gordon Caron, the creator of the series and a close friend of Willis, shared some touching insights about their recent interactions.
Glenn revealed that he has seen Willis’s health decline rapidly. Despite this, Willis remains enthusiastic about the comeback of “Moonlighting.” Glenn confessed that he tries to maintain regular contact with his dear friend and his family, acknowledging the significant impact the illness has had on Willis’s life.
Although Bruce Willis’s condition has affected his ability to communicate verbally, Glenn acknowledges that the essence of Willis remains intact. Glenn marvels at Willis’s recognition when they meet and describes him as a truly remarkable individual. Though he may have lost some linguistic abilities, Glenn emphasizes the enduring spirit of Bruce Willis.
In an interview with the New York Post, Glenn shared his admiration for his friend, highlighting the immense joy for life that Willis possessed. Each day brought enthusiasm and a zest for living to the fullest. It is this spirit that captivated those fortunate enough to spend time with him.
A Journey Filled with Love and Compassion
Bruce Willis’s wife, Emma Heming Willis, has been a pillar of strength throughout his battle with illness. In a recent appearance on the Today show, she bravely discussed the impact of dementia, both on the person diagnosed and their loved ones. Emma, who has two daughters with Bruce, emphasized that receiving a dementia diagnosis is a challenging experience for the entire family.
Emma admits that uncertainty clouds Bruce’s awareness of his illness. However, she finds solace in being the primary caregiver and having a comprehensive understanding of the disease. While it is undoubtedly painful, Emma sees it as both a blessing and a curse – a way to navigate this difficult journey alongside her husband.
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