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The Indonesian teenager has a rare skin condition that doctors in Indonesia have been unable or unwilling to treat and which has left him with an extraordinary appearance.He suffers from Erythroderma, an inflammatory skin disease also known as 'red man syndrome', that causes the skin over almost the entire body to become scaly and flake off. Ari Wibowo has a condition called Erythroderma that makes his skin scaly and flake offAri has shed his skin every 41 days since he was born 16 years ago. He must soak his body in water every hour - night and day - and smear himself with lotion every three hours to prevent drying out.Photographer Nurcholis Anhari Lubis, 35, has documented the little boy’s condition as part of an essay project and describes the boy's skin condition as ‘scaly like a snake about to shed his skin’.‘It’s really sad because he was not born normally and has scaly skin all over his body, similar to being severely burnt, from the sole of his feet up to his head,’ Mr Lubis told Daily Mail Australia.‘

If the boy doesn't moisturise or soak his skin in water, his body would shrivel and harden up like a sculpture and he won't be able to move,' Mr Lubis said.'If he leaves it unattended for too long, he won’t be able to speak because the wrinkles inside his mouth would go hard and it would dry out all his blood in his body.'Mr Lubis said Ari's family were told by doctors at the hospital where he was born that it did not have the resources to treat the condition, and asked them to take the infant away.He and his family now live by a routine of constant washing and dressing his skin with creams.Still, the boy is trying to live a normal life in his village.'He eats normal food like everyone else and his favourite snacks are instant noodles and crackers,' Mr Lubis said.‘He had trouble making friends when he was younger and would often go and play with the other kids but most of the time, they would avoid him because he is different to everyone else.' Ari must contantly wash and moisturise his skin to stop it from drying out

Ari has had trouble making friends because he looked different and people feared his condition may be contagious Photographer Nurcholis Anhari Lubis has documented Ari's life for an essay projectAri is taking lessons, but is forced to study alone because of ignorance about his condition in the community.‘No schools are willing to accept him because they fear his skin condition would be contagious to teachers and other students,' Mr Lubis said.Ari also suffers prejudice because of superstitions in his village.Mr Lubis said many people blame Ari's condition on a superstition that if a woman mistreats animals while she is pregnant then it will affect her unborn child.Some people believe Ari's mother ‘tortured a lizard’ she found in the family home when she was pregnant with Ari.‘I do not believe the myths but in Indonesia, there are still a lot of people who believe this,’ Mr Lubis said.Jakarta-based Mr Lubis spent four days with the little boy and his family.‘When I approached Ari for a photo shoot, he looked very shy but didn't feel embarrassed and was happy to share his story,’ he said.‘