Persons affected by leprosy and their representative organisations are looking for a space within the disability sector through which they can have their voices heard and their rights accessed.

Developing guidelines for leprosy centres and health centres to promote and support self-care with a particular emphasis on prevention of recurrence of ulcers in the community.

A look at our work to train leprosy-affected advocates who can speak on their own behalf

Samir has a wife and two children. He was diagnosed with leprosy at 16 and now he runs his own motorcycle business.

The committee guides our research work to where it is needed the most