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Leprosy in India

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Leprosy in India

Leprosy currently affects approximately a quarter of a million people throughout the world, with majority of these cases being reported from India.[1]

Transmission, treatment and disability

Leprosy is one of the least infectious diseases mainly because nearly all of the population have natural immunity against it.[2] Nevertheless, stigma against the disease due to its disfiguring effects causes its victims to be isolated and shunned. Leprosy is also the leading cause of permanent disability in the world and is primarily a disease of the poor.

The disease is now readily treatable with multi-drug therapy, which combines three drugs to kill the pathogen and cure the patient.[3] If MDT is used in the early stages of infection, disability and disfigurement can be avoided. Unfortunately, even with these facts, individuals with leprosy are still shunned, isolated, and stigmatized so that the fear of leprosy is worse than the disease itself.[4]


India is considered the point of origin of leprosy with skeletal evidence of the disease dating to 2000 B.C.[5] the disease is thought to have spread through trade and war to other parts of Asia, the Middle East, North Africa, and later Europe and the Americas. In ancient Indian society, individuals suffering from leprosy were alienated because the disease was chronic, contagious, resulted in disfigurement, had no cure at the time, and was associated with sin.[6] In colonial India, the government enacted the Leprosy Act of 1898, which institutionalized leprosy victims and separated them based on gender to prevent reproduction. These laws mainly affected the poor because those who were self-sufficient were not obligated to be isolated or seek medical treatment. In the 20th century, even when drugs to treat leprosy became available and more knowledge was gained about the disease, the scourge of leprosy remains a persistent and widespread health problem throughout all regions of the country.

Legal discrimination

The historical legacy and societal stigma toward leprosy are evidenced by various laws containing discriminatory clauses against leprosy victims. Laws in the states of Chhattisgarh, Rajasthan, Madhya Pradesh, Andhra Pradesh, and Orissa prohibit leprosy patients from running in local elections.[7] These laws have been supported by the national government, as evidenced when India's Supreme Court upheld a ruling by the state of Orissa prohibiting leprosy patients from participating in local elections.

Other laws include the Motor Vehicle Act of 1939 which restricts leprosy patients from obtaining a driving license and the Indian Rail Act of 1990 which prohibits leprosy patients from traveling by train.[8]

Many of these laws were written before the development of multi-drug therapy (MDT) and they have not been updated since. For example, almost all of the marriage and divorce laws of India consider leprosy as grounds for divorce with the Special Marriage Act of 1954 declaring leprosy "incurable." These laws do not reflect the current understanding of leprosy.

See also


  1. ^ WHO (September 2011). "Leprosy update, 2011". Weekly Epidemiological Record 36: 389–400. 
  2. ^ World Health Organization (2009): Leprosy.
  3. ^ World Health Organization (2009): Leprosy.
  4. ^ Bhattacharya, S. and Virendra N. Sehgal (1999): Leprosy in India. Clinics in Dermatology 17: 159–170
  5. ^ Robbins, G. et al. (2009): Ancient Skeletal Evidence for Leprosy in India (2000 B.C.). PLoS ONE 4(5): e5669
  6. ^ Jacob, J. and Carlos Franco-Paredes (2008): The Stigmatization and Control. PLoS Neglected Tropical Diseases 2(1):1–3
  7. ^ Putul, A. (2008): Laws in India Criminalise Leprosy.OneWorld South Asia.
  8. ^ Putul, A. (2008): Laws in India Criminalise Leprosy. OneWorld South Asia.

External links

  • WHO Leprosy Factsheet
  • Laws in India Criminalize Leprosy
  • Anandwan

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