“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
Girl’s letter to her future self, written months before she passed away
What most teenagers dream of is to go to college, travel the world, and have many friends. 12-year-old Taylor Smith, of Johnson City, Tennessee, was no different. This girl spent her days around her family and friends and loved watching a lot of Doctor Who.
Smith outlined these plans in a letter she wrote to her future self in April 2013. The letter was placed inside a box in her room with the instruction “To be opened by Taylor Smith on April 12, 2023 only (unless said otherwise).”
Unfortunately, she didn’t live long enough to see whether those dreams would be accomplished. Just months after she wrote that letter, Taylor died of complications from a sudden onset of pneumonia.
Her parents, Tim and Mary Ellen Smith, were heartbroken. They couldn’t believe their girl was forever gone.
One day, as they were sorting through her possessions, they found the letter. As it touched them deeply, they decided to share it online and give others some solace.
As she shared her daughter’s letter, Marry Ellen wrote: “I can’t physically resurrect her, I can’t bring her back, but
I’m so grateful people have been inspired by her story.”
Below is Taylor’s letter and the words she wrote to herself.
Dear Taylor,
How’s life? Life is pretty simple right now (10 years in your past). I know I’m late for you, but as I’m writing, this is early, so; congratulations on graduating high school! If you didn’t, go back and keep trying. Get that degree! Are you (we) in college? If not, I understand. We do have pretty good reasoning, after all.
Don’t forget, it’s Allana’s 11th birthday today! Sheesh, 11 already? In my time, she just turned 1! I didn’t get to go to that party though, because I was in Cranks, Kentucky for my first mission trip. I’ve only been back for 6 days!
Speaking of, how’s your relationship with GOD? Have you prayed, worshipped, read the bible, or gone to serve the lord recently? If not, get up and do so NOW! I don’t care what point in our life we’re in right now, do it! He was mocked, beaten, tortured, and crucified for you! A sinless man, who never did you or any other person any wrong!
Now, have you gone on any more mission trips? Have you been out of the country yet? How about on a plane?
Is Doctor Who still on the air? If not, what regeneration did they end it with? You should go watch some Doctor Who! Later though, you gotta finish reading your own words of wisdom!
Do you have your own place yet? If we’re in college, what are we majoring in? Right now, I wanna be a lawyer.
Have you been to Dollywood recently? Right now, their newest attraction is the Wild Eagle. It’s so fun!
Also I think I’m going to sell my iPad and buy an iPad mini, Don’t forget to tell your kids that we’re older than the tablet! Attached I also have a drawing of an iPad, so you can show them.
Well, I think that’s all. But remember, it’s been 10 years since I wrote this. Stuff has happened, good and bad. That’s just how life works, and you have to go with it.
Sincerely, Taylor Smith
Beautiful words from an angel who was taken away from her family too soon!
If you were touched by Taylor’s words as much as we were, please share this story in her memory.
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