MORHAN
MORHAN is a non-profit organization based in Brazil that advocates for the rights of people affected by Hansen's disease, also known as leprosy. The organization was founded in 1981 by Francisco Augusto Vieira (Chico Mota), a former leprosy patient, and other activists. MORHAN, which stands for Movement for the Reintegration of People Affected by Hanseniasis, works to eliminate the stigma associated with the disease and to ensure that patients receive proper medical care and social support.
History[edit | edit source]
MORHAN was established in 1981 by Francisco Augusto Vieira (Chico Mota), a former leprosy patient, and other activists. The organization was founded in response to the widespread stigma and discrimination faced by people affected by Hansen's disease in Brazil. Since its inception, MORHAN has been instrumental in advocating for the rights of leprosy patients and working towards the elimination of the disease.
Activities[edit | edit source]
MORHAN carries out a range of activities aimed at supporting people affected by Hansen's disease. These include:
- Advocacy: MORHAN advocates for the rights of people affected by Hansen's disease at both the national and international level. The organization works to ensure that patients receive proper medical care and social support, and that they are not discriminated against due to their condition.
- Education: MORHAN provides education and information about Hansen's disease to the public. This includes information about the symptoms of the disease, how it is transmitted, and how it can be treated.
- Support: MORHAN provides support to people affected by Hansen's disease and their families. This includes providing emotional support, as well as assistance with accessing medical care and social services.
Impact[edit | edit source]
MORHAN has had a significant impact on the lives of people affected by Hansen's disease in Brazil. The organization has been successful in reducing the stigma associated with the disease and in ensuring that patients receive the care and support they need. In addition, MORHAN's advocacy efforts have led to changes in government policy and legislation related to Hansen's disease.
See also[edit | edit source]
References[edit | edit source]
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