Abstract
The introduction sets the context and frames the research concern. It highlights the rationale for a focus on human immunodeficiency virus (HIV) in black South African women as a problem of public health and social justice. It offers a broad sketch of relevant debates in policy and in the extant literature, and then locates the work within the lacuna. It articulates the aims and scope of the work, and briefly discusses the theoretical framework used to conceptualise and investigate the research problem: Amartya Sen’s capabilities approach. The final part of the introduction offers a thumbnail sketch of the chapters to come.
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Notes
- 1.
Health science publications typically seek the latest available data. Robust data from low- and middle-income countries (LMIC) settings are not always available, however. Publications cited in this work are those that specifically track, analyse and offer comparative data on key trends in particular population groups in these settings (such as women generally, African women, or young women aged 15–24). These publications may be several years old and still constitute the latest data. Additionally, the key (high-quality) reports cited and released in South Africa, such as the South African National HIV Prevalence , Incidence and Behaviour and Survey and the National Burden of Disease Study for South Africa, are released typically only every 3–5 years. With other works (e.g. on health equity or gender), I am highlighting significant foundational texts or reports, rather than the latest publication dealing with the subject matter. The dearth of data in LMICs, a theme emerging from the Millennium Development Goals (MDGs) that is reaffirmed in this work, has important ethical and equity dimensions: the lack of and poor-quality data in LMICs raise questions concerning who is counted, and thus whose health and lives matter.
- 2.
Race is a social construct . Today, prominent scientists agree that the biological basis of race is so weak as to require cessation in using racial categories in genetics research: ‘Racial categories are weak proxies for genetic diversity and need to be phased out’ (see Gannon, 2016, p. 1). I employ the racial categories here in the South African context, which were socially constructed, had a highly deleterious impact on people’s life chances and experiences for decades (and which continues for many), and are still in use in data collection, in order for redress to occur (see Gutto, 2002; Habib & Bentley, 2008). These are African or black, coloured, white and Asian.
- 3.
The award-winning author, film director and activist Tsitsi Dangarembga created a short film (17 minutes) that powerfully engages the struggles of a rural Zimbabwean woman seeking to care for a vulnerable AIDS (acquired immune deficiency syndrome) orphan, Tabitha, during the Zimbabwean economic crisis. The film underscores the essential role of family and community in sharing the burden of caring for their most vulnerable members, while highlighting the political determinants of health. The Sharing Day can be seen here: http://tve.org/film/the-sharing-day/.
- 4.
Jong-wook (2003), former director general of the World Health Organization (WHO) (2003–2006), first sought to connect the global ‘Health for All’ campaign to the international HIV epidemic and to WHO’s health equity agenda. Before his death, Jong-wook wrote that the most urgent objectives for WHO included the health-related MDGs and the ‘3 by 5’ targets for HIV/AIDS treatment, which aimed to make essential HIV medication accessible to 3 million people, mainly in the poorest countries, by the end of 2005.
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Sprague, C. (2018). Introduction. In: Gender and HIV in South Africa. Global Research in Gender, Sexuality and Health. Palgrave Macmillan, London. https://doi.org/10.1057/978-1-137-55997-5_1
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