Human Rights and Leprosy
PRAGUE – At the end of last year, the United Nations General Assembly unanimously adopted a resolution approving principles and guidelines to end discrimination against people affected by leprosy and their family members.
This resolution marked the culmination of several years of lobbying of UN institutions by groups and individuals devoted to focusing attention on an overlooked human rights issue: the social discrimination suffered by people diagnosed with leprosy. Indeed, the discrimination usually continues even after they are cured, blighting not only their lives, but the lives of their family members.
For much of its long history, leprosy was feared as an incurable, disfiguring disease. People who came down with it were ejected from their communities. They often ended up in isolated villages or remote islands, condemned by society to spend the rest of their days as social outcasts.
To continue reading, register now.
Already have an account? Log in