She’s called  “monkey face” and  “wolf girl”, but the world’s hairiest girl,12-year-old Supatra Sasuphan, is very happy.
The schoolgirl, whose face is covered in hair through a rare genetic condition which afflicts just 50 people worldwide, initially faced merciless teasing at school in Bangkok.
But rather than let the condition ruin her life, Supatra says she enjoys being a world record holder and is even one of the most popular girls at her school.
She works hard and is one of the better students in her school, and even has ambitions to become a doctor – so she can “look after the sick and her own family”.
Likewise her parents, who found out about her condition when she was born, say she is just “a normal little girl.”

Supatra herself insists her condition is just ‘who I am’, adding that she ‘does not even think about’.

Supatra is one of just 50 known sufferers of Ambras Syndrome – caused by a faulty chromosome – to be documented since the Middle Ages. Before the disease was understood, sufferers were branded ‘werewolves.’

She has thick hair growing over her face, ears, arms, legs and back. Even laser treatment has failed to stop the hair growth.

But while most sufferers have been shunned, Supatra has gradually been embraced by her community, and became a popular and outgoing child.
She said: ‘There were a few people who used to tease me and call me monkey face but they don’t do it any more.
“I’m very used to this condition. I can’t feel the hair as it has always been like this. I don’t feel anything.
“It does sometimes make it difficult to see when it gets long.I hope I will be cured one day.”

“She gets along with others really well and is very generous. She has a lot of friends.”

In other ways Supatra is the same as other children her age – she loves swimming, dancing to her favourite music and playing with friends.
But more than anything, Supatra loves perching in front of the TV at her tiny one-bedroom family home in Pranakom, on the outskirts of Bangkok, to watch cartoons.
She said: “I like to watch anything on TV, whatever is, I like having it on. I like to watch Bugs Bunny.”

The bubbly little girl is also determined not to let her condition prevent her from leading a normal life.
She said: ‘I like to study maths so I can be good at it and teach it to younger children so they can do it too.
‘I want to become a doctor so I can help patients when they get injured.
‘I want to help people who get hurt and help cure people.”

Supatra’s future didn’t always look so promising. When she was first born she had to undergo two operations just to breathe.
Her father Sammrueng, 38, said:  “We found out Supatra’s condition when she was born – we did not know before.
“She was not very healthy because her nostrils were only one millimetre wide. For the first three months she was kept in an incubator to help her breathe.She was in the hospital for a total of ten months. We were very worried about her.”
Supatra has another operation when she was two-years-old and can now breathe normally.
But when Sammrueng and his wife Somphon, 38, brought Supatra home to live with them and their other daughter Sukanya, now 15, they faced more problems.
“When neighbours first saw Nat they asked what kind of sin I had done. I was very worried about what she would be when she grew up because of other children teasing her,” he said.
But Supatra’s sweet nature quickly won over people in her community.
Sammrueng, a jewelery maker, said: ‘She gets along with others really well and is very generous. She has a lot of friends.
‘She is just the same as any other little girl her age.
‘But her teeth grow slowly and she can’t see very well.’
Doctors tried to remove the hair with laser treatment when she was two-years-old but despite numerous sessions it kept growing back as thickly as before.
Supatra’s hair has got increasingly thicker as she has grown up so her mother has to cut it back regularly for her.
She uses baby shampoo to wash her hair as she is allergic to stronger brands.
Sammrueng said: ‘I still hope one day she will be cured. We will do anything we can if it will help her.’
Chris Parsons
Daily Mail 

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