“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
Mia Robertson is overcome with emotion.
Mia Robertson, the actress Missy and actor Jase Robertson’s daughter from Duck Dynasty, lost a very dear person this week.
Her longtime doctor, Dr. David Genecov, was killed in a car crash. Missy Robertson informed her Instagram fans that Mia underwent surgery to repair her fractured palate and lip.
Since Dr. Genecov had been Mia’s doctor for a number of years prior to his passing, his passing has impacted her life.
He not only provided her with medical care, but he was also incredibly compassionate and supportive throughout. His passing has upset Mia and her family, who have loved their time together over the years.
Mia Robertson has been fortunate to have such a knowledgeable and compassionate pediatrician all of her childhood.
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She will always treasure her memories of him, even if his passing has left them all in disbelief and grief. Mia’s heart will always carry Dr. Genecov’s love as a continual reminder that he will never be forgotten.
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Missy Robertson talks about how she and her daughter, Mia Robertson, were affected by her husband’s kindness and unwavering support.
His loving demeanor brought them comfort, and his words of encouragement inspired them to take on any challenge. In July, Mia underwent her fourteenth surgery, which she believes to be the final one she will ever require.
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She established the “Mia Moo Fund” in order to provide healthcare to other kids and free them from having to cover up their smiles due to health issues. Thanks in part to the encouragement of their family and friends who have stood with them through thick and thin, Missy and Mia are more important than ever.
Missy’s husband was polite and helpful, which helped stabilize and bring tranquility to an otherwise chaotic situation. His presence gave Mia the support she needed to face an uncertain future, which enabled her undergo her fourteenth treatment in July without anxiety.
In addition, he helped them become stronger than either of them could have imagined before these difficulties; day by day, they felt more capable of facing any challenges that came their way with bravery and elegance.
As a result of this journey, Mia founded the “Mia Moo Fund,” a nonprofit dedicated to helping kids in need of medical attention by providing financial assistance so they won’t have to give up their smiles for want of funds.
Mia received the heartbreaking news from Missy Robertson. Dr. Genecov left a lasting legacy of elegance and beauty, as well as a passionate desire to involve his patients in decision-making, that those who knew him best will never forget.
Mia considers herself lucky to have connected with Dr. David Genecov. He made an unrivaled contribution to her experience with broken lip and palate, as well as numerous medical advancements that will benefit future generations.
Mia’s mother begged everyone to pray for people who were in agony as a result of this tragedy, saying that she could no longer remember life before her appointment with Dr. David.
The family will always be grateful for the doctor’s contributions to medical advancements that have improved lives all across the world, and they will always have a special place in their hearts for his work and kindness at this difficult time.
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