| Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2015: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2014: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2013: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2012: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2011: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
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| Outline of Final Research Achievements |
In Japan, the policy for Hansen’s disease patients began from when the government enacted “law No.11（Matter concerning the prevention of leprosy ）”in 1907 .In 1931, the enactment of “Leprosy Prevention Law” changed to absolute segregation of all leprosy patients that may be contagious. This law underwent amendments and existed up to 1996. The reason why wrong policies was continued for a long period of about 90 years is not clarified enough. The purpose of this study is to clarify the truth about alienation from international tendency through the historical study of social work for Hansen’s disease patients during 1920～1940,focusing on conflict between abusolute segregation and parole system.
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