Leprosy segregation
Date and country of first publication[1][edit | edit source]
1993
United Kingdom
Definition[edit | edit source]
Leprosy segregation refers to the historical practice of isolating and segregating individuals with leprosy from the rest of society. This practice dates back to ancient times and was based on the fear and misconception that leprosy was highly contagious.
In many cultures, people with leprosy were forced to live in leper colonies or leprosariums, which were isolated communities where they were removed from the general population. They were often treated as outcasts and faced stigma, discrimination, and social ostracism.
However, with advancements in medical knowledge and treatment, it is now understood that leprosy is not highly contagious and can be effectively treated with antibiotics. As a result, leprosy segregation is no longer considered necessary or ethical, and efforts are being made to integrate individuals affected by leprosy back into society and combat the stigma associated with the disease.
See also[edit | edit source]
References[edit | edit source]
Notes[edit | edit source]
- ↑ Date and country of first publication as informed by the Scopus database (December 2023).
At its current state, this definition has been generated by a Large Language Model (LLM) so far without review by an independent researcher or a member of the curating team of segregation experts that keep the Segregation Wiki online. While we strive for accuracy, we cannot guarantee its reliability, completeness and timeliness. Please use this content with caution and verify information as needed. Also, feel free to improve on the definition as you see fit, including the use of references and other informational resources. We value your input in enhancing the quality and accuracy of the definitions of segregation forms collectively offered in the Segregation Wiki ©.
Leprosy segregation appears in the following literature[edit | edit source]
Duncan M.E. (1993). An historical and clinical review of the interaction of leprosy and pregnancy: A cycle to be broken. Social Science and Medicine, 37(4), 457-472. https://doi.org/10.1016/0277-9536(93)90281-8
Sato H., Narita M. (2003). Politics of leprosy segregation in Japan: The emergence, transformation and abolition of the patient segregation policy. Social Science and Medicine, 56(12), 2529-2539. Elsevier Ltd.https://doi.org/10.1016/S0277-9536(02)00285-X
Pandya S.S. (2003). The first international leprosy conference, Berlin, 1897: the politics of segregation.. História, ciências, saúde--Manguinhos, 10(Suppl 1), 161-177. https://doi.org/10.1590/s0104-59702003000400008
Miyasaka M. (2014). The justice of listening: Japanese leprosy segregation. We Shall Bear Witness: Life Narratives and Human Rights, 100-117. University of Wisconsin Press.https://doi.org/