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Effects of HIV-related stigma among an early sample of patients receiving antiretroviral therapy in Botswana 

Authors: W. R. Wolfe a;  S. D. Weiser a;  D. R. Bangsberg a;  I. Thior b;  J. M. Makhema b;  D. B. Dickinson b;  K. F. Mompati b; R. G. Marlink c
Affiliations:   a University of California, San Francisco
b Botswana-Harvard School of Public Health Partnership, Gaborone, Botswana
c Harvard School of Public Health AIDS Initiative, Boston, USA
DOI: 10.1080/09540120500333558
Publication Frequency: 12 issues per year
Published in: journal AIDS Care, Volume 18, Issue 8 November 2006 , pages 931 - 933
Formats available: HTML (English) : PDF (English)
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Abstract

Botswana, with its estimated HIV prevalence of 37%, instituted a policy of universal access to antiretroviral therapy (ART) in 2002. Initial enrolment lagged behind expectations, with a shortfall in voluntary testing that observers have attributed to HIV-related stigma - although there are no published data on stigma among HIV-positive individuals in Botswana. We interviewed 112 patients receiving ART in 2000, finding evidence of pervasive stigma in patterns of disclosure, social sequelae, and delays in HIV testing. Ninety-four percent of patients reported keeping their HIV status secret from their community, while 69% withheld this information even from their family. Twenty-seven percent of patients said that they feared loss of employment as a result of their HIV status. Forty percent of patients reported that they delayed getting tested for HIV; of these, 51% cited fear of a positive test result as the primary reason for delay in seeking treatment, which was often due to HIV-related stigma. These findings suggest that success of large-scale national ART programmes will require initiatives targeting stigma and its social, economic and political correlates.
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