Meet 'Tree Man', the young man with branch-like limbs with a disease so rare doctors were left speechless on Body Bizarre
WARNING: This video and article contains graphic content.
Abul, a young man who suffers from an uncontrollable 'tree-like' growth, was told he only had one option by doctors in an episode of Body Bizarre.
In the series – which you can watch for free on 9Now – Abul, who was 25 at the time of filming, explained how one of the world's rarest diseases has affected his everyday life.
Stream episode of Body Bizarre for free on 9Now.
"Sometimes I wonder why God has given me such a dreadful condition," he told cameras.
To paint a picture, Abul has massive branch-like structures encasing his hands and feet. Without proper treatment, his disease would only spread.
"It makes me uncomfortable that I cannot stand or sit in one place. It just drives me crazy," he said.
You can hear more of Abul's story in the video above.
Abul suffers from one of the rarest conditions in the world. Nine
Nicknamed 'Tree Man', Abul lives with an extremely rare condition known as epidermodysplasia verruciformis, which causes HPV to grow uncontrollably and leads to the development of warts resembling tree bark.
The debilitating disease meant Abul couldn't work, feed himself or even visit the toilet alone.
Abul dreams of a normal life. Nine
"I feel awful about my fate," said the young man from Bangladesh.
"People suffer from different illnesses, they get well or they die. That's the end of their suffering," he said.
Abul's condition has been a "burden" on his life and the life of his family. Nine
Abul is married, and has a three-year-old daughter. He hopes to one day provide for his family, let alone use his hands for the first time in five years.
"My own hands and legs are a burden," he said.
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Doctors hope to remove the warts and create a functional hand for Abul. Nine
For the first time doctors hoped to perform a life changing surgery by removing Abul's growths and separate two or three fingers.
His doctor, Dr Samanta Lal Sen, said he had never seen a patient like Abul. But their research, not long ago, revealed a similar case in Indonesia.
In fact, the disease is so rare, it had only been seen before four times worldwide at the time of filming.
You can hear more about the unique case in the video below.
Abul was told that surgery was the only option to remove his excessive growths. But stepping into the unknown, the surgery had its risks.
Head of plastic surgery, Prof Abul Kalam, was also concerned about Abul's overall fitness for surgery. Mainly his " chronic malnutrition."
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Dr Samanta Lal Sen said this was the first time Bangladesh had ever seen anything like this. Nine
Ultimately they came to a decision that would hopefully help Abul achieve his one dream: "To do something for the future of my baby daughter," he shared.
To find out what decision the doctors came to, watch Abul's full story on Body Bizarre in the episode 'Tree Man' on 9Now.
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