Kit Blog

Self Care and Self Help Groups

16 May 2016 | Author: Andrew Hateley-Browne

Once someone develops a chronic condition (such as a loss of sensation) because of leprosy, they need to take regular care in all activities of daily living and work. Because this is such an extensive and life-long undertaking, it’s better for people affected by leprosy to take responsibility of their condition. This is why you support the implementation of Self Care and Self Help Groups in Timor Leste, Nepal, Nigeria and India. They’re small communities of people affected by leprosy who care, support and advocate for each other.

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Understanding Reaction

15 Feb 2016 | Author: Andrew Hateley-Browne

Reaction is a common complication that can arise when someone has leprosy—sometimes as late as seven years afterwards. It’s an episode of inflammation that affects a third of all leprosy patients. It can result in extensive nerve damage and is the major cause of disability in leprosy. It’s unfortunate for patients that begin to recover from leprosy only to experience further irreversible damage from Reaction. It’s one of the things that makes leprosy such a complex and harmful disease.

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Understanding leprosy

08 Feb 2016 | Author: Andrew Hateley-Browne

Leprosy is a disease that affects people differently according to their immunity to certain bacteria. 5% of people have no immunity. It seems like a category, but it’s more of a spectrum. Some people in that 5% have a small immune response. Others have none. The World Health Organisation has organised these differences under two classifications: Paucibacillary leprosy and Multibacillary leprosy. These classifications have their own symptoms and medical response. Leprosy can be described even further with several sub-types that sit along the Ridley-Jopling Scale. With so many sub-types and symptoms, it’s hard to believe they’re all caused by two simple organisms—M.leprae and M.lepromatosis.

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Life on Fantome Island: The Joe Eggmolesse story

25 Jul 2015 | Author: Andrew Hateley-Browne

Joe Eggmolesse is a third-generation Australian South Sea Islander. His grandparents came by ship to Australia in the late 1800s. His grandfather came willingly. But his grandmother, at 16 years of age, was taken by force in a practice called “blackbirding”. In Queensland and northern New South Wales, the sugar and cotton industries enslaved islanders. Around 60,000 people came to Australia as “indentured labourers” in this way. In 1901, the government enacted two White Australia policies. They tried to get rid of “Kanakas” (South Sea island workers). After half a century of blackbirding, the practice finally stopped.

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