Case Studies

Bento, Mozambique?width=216&height=130&mode=crop

Bento, Mozambique

One of our projects in Mozambique supports members of the Association for People Affected by Leprosy (ALEMO) to raise their profile in the community, to educate people about leprosy and promote inclusion. ALEMO group members are also supported in developing livelihoods and greater food security. Click here to read full story

A valuable experience?width=216&height=130&mode=crop

A valuable experience

Medical student Anna Wilson followed in her grandparents' footsteps by working at The Leprosy Mission's Anandaban Hospital in Nepal. The Birmingham University student worked with leprosy patients at the hospital set on the side of a hill twenty miles south of Kathmandu for seven weeks last summer. Click here to read full story

Mohammad, India?width=216&height=130&mode=crop

Mohammad, India

Mohammad is 16 years old and experienced the first symptoms of leprosy at the age of nine. He had skin patches that had lost both colour and sensation, but was unfortunately misdiagnosed with a different disease. Click here to read full story

Vitrendra, India?width=216&height=130&mode=crop

Vitrendra, India

Vitrendra is 63 years old and has lived in a leprosy colony in Bareilly for 40 years. He came to live there because he felt guilty for having leprosy and wanted to move to a place where no-one knew him. Before arriving there he did not know that leprosy colonies existed. Click here to read full story

Hotrika, India ?width=216&height=130&mode=crop

Hotrika, India

Hotrika, 20, is from India’s Chhattisgarh state. When she was at school she noticed patches on her hands. There is much stigma surrounding leprosy in India and her mother discreetly took her to see a doctor. Leprosy was diagnosed and multidrug therapy started. Click here to read full story

Parvin, Bangladesh ?width=216&height=130&mode=crop

Parvin, Bangladesh

Bangladesh is a male-dominated society where women with disabilities - particularly those with leprosy - are vulnerable. We are an integral partner of a food security project working with 40,000 female-headed households to ensure women affected by leprosy can provide for themselves and their families. Click here to read full story

Hadjara, Niger ?width=216&height=130&mode=crop

Hadjara, Niger

The water tower installed at Danja Hospital by The Leprosy Mission ensures a fresh water supply for patients as well as leprosy-affected communities living near to the hospital site. In Danja village Hadjara Souley, 60, collects a nominal payment of five francs for every 30 litres of water collected from the pump. Click here to read full story

Manju, India ?width=216&height=130&mode=crop

Manju, India

Manju Roy first showed signs of leprosy soon after her marriage, aged 14. There is real stigma surrounding leprosy in her home city of Kolkata and Manju did not seek treatment for the disease when she first noticed light patches on her skin. Click here to read full story

Nafisa, Nigeria ?width=216&height=130&mode=crop

Nafisa, Nigeria

Nafisa Aminou, 20, is from Nigeria and was told, aged 14, she had leprosy and was advised to go to hospital for treatment. But instead she was given traditional herbal treatment for five years. If she was given multidrug therapy at an early stage, it would have been highly unlikely that she would have become disabled. Click here to read full story

Jugdha, India ?width=216&height=130&mode=crop

Jugdha, India

There are 850 leprosy colonies in India. In the past 15 years the Indian government has built no new colonies so leprosy-affected people live in regular villages. This is why it is imperative for the Challenging Anti-Leprosy Legislation (CALL) project to educate villagers on the human rights of leprosy-affected people and to stamp out any stigma within the community. Click here to read full story

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