Indian girl, 16, who sheds her skin every six weeks

A ‘human snake’ teenager who sheds her skin every six weeks because of a rare condition is set to get life-improving treatment in Europe.

Shalini Yadav, 16, needs to constantly smear her body with moisturiser and have a bath every hour to stop it from hardening and seizing up.

But her family are so poor they couldn’t afford any specialist treatment to ease her ailments, leaving her unable to walk without a stick or straighten her limbs.

Local fundraisers heard about her painful existence and alerted hospitals around the world – including one in Spain who has now agreed to treat Shalini for free.

The teenager, from Nowgong town in Chattarpur district of the central Indian state of Madhya Pradesh, will fly to Spain tomorrow for treatment.

Shalini Yadav, 16, needs to constantly smear her body with moisturiser and have a bath every hour to stop it from hardening and seizing up

She said: ‘I was very excited to learn that we’d be going to Spain. I have seen the place in an Indian TV show – now I will actually get to see it. 

Doctors have diagnosed Shalini with erythroderma, an inflammatory skin disease also known as ‘red man syndrome’, but were unable to treat it. 

It causes the skin over almost the entire body to become scaly and flake off and Shalini has shed her skin every 45 days since she was born, reports suggest.

She has to soak her body in water every hour – night and day – and smear himself with lotion every three hours to prevent drying out.

But her family are so poor they couldn't afford any  treatment to ease her ailments, leaving her unable to walk without a stick or straighten her limbs (pictured with her mother Devkunwar)

But her family are so poor they couldn’t afford any  treatment to ease her ailments, leaving her unable to walk without a stick or straighten her limbs (pictured with her mother Devkunwar)

Local fundraisers heard about her painful existence and alerted hospitals around the world - including one in Spain who has now agreed to treat Shalini for free

Local fundraisers heard about her painful existence and alerted hospitals around the world – including one in Spain who has now agreed to treat Shalini for free

ERYTHRODERMA: THE FACTS

Non-bullous ichthyosiform erythroderma is an extremely rare skin disorder,characterised by abnormal scaling of the skin with underlying redness.

It is estimated to occur in one in 300,000 births.

The skin appears bright red, and has accompanying fine white or flesh coloured scales. The scales are often seen all over a sufferer’s body, but the skin on the face may show milder changes. 

The incurable condition is usually detected in the first few days of life, and is a life-long condition for most sufferers. 

It is caused by a genetic or inherited abnormality that affects normal skin shedding. 

One in four children will inherit two abnormal genes – one from each parent – and therefore develop the condition. 

Source: Ichthyosis Support Group  

Her mother Devkunwar said: ‘I feel so helpless when I see her skin coming off, causing excruciating pain to my child.

‘This disease is not killing her but taking her life bit by bit. We have no idea where to go to and who to consult.’ 

Devkunwar, a carer in a state-funded community centre, is so heart-broken she says death would be kinder to her daughter.

She added: ‘It is better to die than living a life of misery.’ 

Shalini’s two siblings Sejal, 15, and Price, eight, are deemed medically healthy with no such complication. 

Her father Rajbahadur, a daily wage worker, said: ‘It’s really sad because she was not born normally and has scaly skin all over her body.

‘It is similar to being severely burnt, from the sole of her feet to her head.’ 

Shalini got help after India-based press agency Newslions highlighted her plight. It has since helped pay for her expenses.

She is being treated for free at Regional University Hospital and Virgen de la Victoria of Malaga. Doctors hope she will be able to walk without a stick after the treatment.

Rajbahadur added: ‘I am very grateful for all that the hospital from Spain is offering. Without their help… my daughter would never get a shot at leading a normal life.’ 

The teenager, from Nowgong town in Chattarpur district of the central Indian state of Madhya Pradesh, will fly to Spain tomorrow for treatment

Doctors have diagnosed Shalini with erythroderma, an inflammatory skin disease also known as 'red man syndrome', but were unable to treat it

The teenager, from Nowgong town in Chattarpur district of the central Indian state of Madhya Pradesh, will fly to Spain tomorrow for treatment

Her father Rajbahadur (pictured left), a daily wage worker, said: 'It's really sad because she was not born normally and has scaly skin all over her body'

Her father Rajbahadur (pictured left), a daily wage worker, said: ‘It’s really sad because she was not born normally and has scaly skin all over her body’

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