A Human Rights Approach to TB - Stop TB Partnership
A Human Rights Approach to TB - Stop TB Partnership
A Human Rights Approach to TB - Stop TB Partnership
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20<br />
<strong>to</strong> define some of the structural connections between health and human rights.<br />
The first WHO global response <strong>to</strong> AIDS in 1987 called for human rights for<br />
people living with HIV/AIDS. This was the first time human rights were<br />
explicitly named in a public health strategy.<br />
Throughout the course of the HIV/AIDS pandemic it has been shown<br />
“that public health efforts <strong>to</strong> prevent and control the spread of HIV/AIDS are<br />
more likely <strong>to</strong> succeed in public health terms if policies and programmes<br />
promote and protect human rights.” 48<br />
The dual epidemic of HIV and <strong>TB</strong> raises issues of individual choice and<br />
confidentiality.<br />
In many countries, preserving confidentiality about one’s HIV or <strong>TB</strong> status<br />
is difficult. Merely visiting a <strong>TB</strong>- or HIV-associated clinic can arouse community<br />
suspicion and begin a cycle of stigmatization. This can act as a<br />
deterrent <strong>to</strong> diagnosis. Individuals have a right <strong>to</strong> privacy that protects them<br />
against both manda<strong>to</strong>ry testing and disclosure of their health status. They also<br />
have a right <strong>to</strong> education and information about <strong>TB</strong>, HIV, and the synergy<br />
between the two infections so that they can make informed choices about<br />
testing and treatment options.<br />
Informed, voluntary testing of <strong>TB</strong> patients for HIV is being encouraged by<br />
a community-based initiative implemented at several district-level sites in<br />
Africa called ProTEST. ProTEST attempts <strong>to</strong> reach some of the 90 per cent of<br />
people with HIV who do not know they are HIV-positive, and provide them<br />
with access <strong>to</strong> preventive treatment for <strong>TB</strong> if they have not yet developed it.<br />
ProTEST’s goal is <strong>to</strong> create an environment in which more people will choose<br />
<strong>to</strong> be tested for HIV. This is being done, in part, by taking a rights-based<br />
approach that emphasizes counselling and education. The name reflects the<br />
dual aims of promoting voluntary testing and mobilizing communities <strong>to</strong><br />
protest for better <strong>TB</strong> and HIV care. It is hoped that when patients understand<br />
that if they know they are HIV-positive they will have access <strong>to</strong> a full range of<br />
HIV care and treatment services—including <strong>TB</strong> screening, prevention, and<br />
treatment—this new knowledge will counterbalance the stigma associated<br />
with HIV.<br />
48. Gruskin, S. and D. Taran<strong>to</strong>la,<br />
HIV/AIDS, Health and <strong>Human</strong><br />
<strong>Rights</strong>, chapter 29. In: Handbook<br />
on HIV/AIDS. Family Health<br />
International (in press)