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Leprosy has historically been associated with social stigma, which continues to be a barrier to self-reporting and early treatment. [4] Leprosy is classified as a neglected tropical disease. [21] World Leprosy Day was started in 1954 to draw awareness to those affected by leprosy. [22] [4] The study of leprosy and its treatment is known as ...
It promotes the understanding, identification and treatment of Hansen's disease (leprosy) by creating and maintaining museum displays, traveling exhibits, publications and a web site in order to educate and inform the public. [37]
June Berthelsen was another patient on the island, having been diagnosed with Hansen's disease in 1956. [31] Her memoir, The Lost Years: A Story of Leprosy, documents her experiences as a sufferer of Hansen's disease, and details her period on the island between 1956 and mid-1958. She was the only patient to have written a personal account ...
In the 21st century, this term is falling into disuse as a result of the diminishing number of leprosy patients. Because of the stigma to patients, some prefer not to use the word 'leprosy', preferring 'Hansen's disease'. The term 'leprosy' is still used by the U.S. Centers for Disease Control and Prevention and the World Health Organization. [7]
In 1999, the world incidence of Hansen's disease was estimated to be 640,000. In 2000, 738,284 new cases were identified. [5] In 2000, the World Health Organization (WHO) listed 91 countries in which Hansen's disease is endemic. India, Myanmar and Nepal contained 70% of cases. India reports over 50% of the world's leprosy cases. [6]
Mycobacterium leprae (also known as the leprosy bacillus or Hansen's bacillus) is one [a] of the two species of bacteria that cause Hansen's disease (leprosy), [1] a chronic but curable infectious disease that damages the peripheral nerves and targets the skin, eyes, nose, and muscles.
The hotline settles doubts about the disease, directs people to the places of treatment around Brazil, and receives complaints of lack of drugs, prejudice, lack of care, and abuse. [3] Morhan volunteers and members are responsible for manufacturing shoes for people with leprosy with the support of an Italian non-governmental organization. [11]
Paul Wilson Brand, CBE (17 July 1914 – 8 July 2003) was a pioneer in developing tendon transfer techniques for use in the hands of those with leprosy.He was the first physician to appreciate that leprosy is not a disease of the tissue but of the nerves: it is the loss of the sensation of pain which makes sufferers susceptible to injury and leads to tissue rotting away, especially in the ...