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Lachhu showed obvious outward signs of leprosy

Lachhu lived with her family in the Adilabad district of India. When she began to develop patches on her skin at first she paid no attention to them. But gradually the disease progressed and as her fingers became clawed, she was unable to perform her day-to-day activities.

These deformities marked her out as an obvious case of leprosy and there was deep rooted stigma in the village.

Despite protests from her family they were powerless to stop the village elders from throwing Lachhu out. She was ostracised by her community and for 15 years was forced to live alone in a shed a mile outside the village. Her family had to accept that the villagers hated her because they feared being infected.

Health education is a vital role for LEPRA When a community health worker discovered Lachhu living alone and in poverty he informed LEPRA of her plight. LEPRA held several meetings with the elders to persuade them that leprosy is not spread by touch and was a curable disease. Six sessions of street theatre, puppetry, ‘video van’ screenings and leaflets were used to educate the villagers. Gradually, through education, their perception of leprosy changed.

LEPRA also provided her with medical treatment, physiotherapy and footwear. As a result of the education programme, the villagers were persuaded to accept Lachhu back into their community. She is now reunited with her family and has been able to return to her home.

Thanks to the work of LEPRA, Lachhu is now back with her children and grandchildren.

Your support for LEPRA helps to ensure that more families are able to stay together.

The more we can reach out and educate communities, the less people will suffer the terrible rejection & stigma often experienced by those with leprosy, HIV or lymphatic filariasis.

Your support for LEPRA can help to ensure that more families are able to stay together.

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