"My mother told me that I should not": a qualitative study exploring the restrictions placed on adolescent girls living with HIV in Zambia

被引:25
作者
Mackworth-Young, Constance R. S. [1 ,2 ]
Bond, Virginia [1 ,2 ]
Wringe, Alison [3 ]
Konayuma, Katongo [2 ]
Clay, Sue [4 ]
Chiiya, Chipo [4 ]
Chonta, Mutale [4 ]
Sievwright, Kirsty [5 ]
Stangl, Anne L. [5 ]
机构
[1] London Sch Hyg & Trop Med, Fac Publ Hlth & Policy, Dept Global Hlth & Dev, London, England
[2] Zambart, Social Sci Dept, Lusaka, Zambia
[3] London Sch Hyg & Trop Med, Fac Epidemiol & Populat Hlth, Dept Populat Hlth, London, England
[4] 3Cs Reg Consultants, Lusaka, Zambia
[5] Int Ctr Res Women, Washington, DC USA
关键词
Adolescents; stigma; adherence; social support; young women; adolescent girls; adolescents living with HIV; disclosure; sexual relationships; Zambia; REPRODUCTIVE HEALTH; SOCIAL REPRESENTATIONS; ANTIRETROVIRAL THERAPY; SOUTH-AFRICA; GROWING-UP; RESPONSIBILITY; ACQUISITION; PREVENTION; NARRATIVES; ADHERENCE;
D O I
10.1002/jia2.25035
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Adolescent girls in sub-Saharan Africa are disproportionately affected by HIV due to a range of social and structural factors. As they transition to adulthood, they are recipients of increasing blame for HIV infection and 'improper' sex, as well as increasing scrutiny, restrictions and surveillance. This study used a qualitative and participatory approach to explore the messaging and restrictions imposed on adolescent girls living with HIV in Zambia. Methods: Thirty-four in-depth interviews and four participatory workshops were carried out with 24 adolescent girls aged 15 to 19 years old living with HIV in Lusaka, Zambia. Key themes explored included experiences living with HIV, finding out about HIV status, disclosure, experiences with antiretroviral treatment, and support needs. Data were organized, coded and analysed using a grounded theory approach to thematic analysis. This analysis uses data on participants' experiences of living with HIV and their interactions with their parents, guardians and healthcare providers. Results: Family and healthcare providers, partly in a quest to protect both the health of adolescent girls living with HIV and also to protect them from blaming discourse, imposed restrictions on their behaviour around three main topics: don't disclose your HIV status, don't have sex, and don't miss your medicines. These restrictions were often delivered using tactics of fear, and usually disconnected from other options. Participants responded to these messages in several ways, including internalizing the messages, changing their behaviour either to comply with or resist the restrictions, by remaining silent and anxious when restrictions were broken, and developing concerns around their own health and sexual and reproductive aspirations. Participants also sometimes experiencing stigma when restrictions could not be maintained. Conclusions: Restrictive messages were delivered to adolescent girls living with HIV through the broader social discourses of stigma, religion, and global and local narratives about HIV. Programmes aiming to support adolescent girls living with HIV need to work together with parents and healthcare providers to reflect on the impact of sanctioning messages, and to encourage more enabling and empowering messaging for adolescent girls living with HIV.
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页数:7
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  • [1] When information does not suffice: young people living with HIV and communication about ART adherence in the clinic
    Bernays, S.
    Paparini, S.
    Gibb, D.
    Seeley, J.
    [J]. VULNERABLE CHILDREN AND YOUTH STUDIES, 2016, 11 (01) : 60 - 68
  • [2] "Not Taking it Will Just be Like a Sin": Young People Living with HIV and the Stigmatization of Less-Than-Perfect Adherence to Antiretroviral Therapy
    Bernays, Sarah
    Paparini, Sara
    Seeley, Janet
    Rhodes, Tim
    [J]. MEDICAL ANTHROPOLOGY, 2017, 36 (05) : 485 - 499
  • [3] What am I 'living' with? Growing up with HIV in Uganda and Zimbabwe
    Bernays, Sarah
    Seeley, Janet
    Rhodes, Tim
    Mupambireyi, Zivai
    [J]. SOCIOLOGY OF HEALTH & ILLNESS, 2015, 37 (02) : 270 - 283
  • [4] Children growing up with HIV infection: the responsibility of success
    Bernays, Sarah
    Jarrett, Prudence
    Kranzer, Katharina
    Ferrand, Rashida A.
    [J]. LANCET, 2014, 383 (9925) : 1355 - 1357
  • [5] Bond V, 2003, LIGHTS IS UNDERSTAND
  • [6] Good Health and Moral Responsibility: Key Concepts Underlying the Interpretation of Treatment as Prevention in South Africa and Zambia Before Rolling Out Universal HIV Testing and Treatment
    Bond, Virginia
    Hoddinott, Graeme
    Viljoen, Lario
    Simuyaba, Melvin
    Musheke, Maurice
    Seeley, Janet
    [J]. AIDS PATIENT CARE AND STDS, 2016, 30 (09) : 425 - 434
  • [7] "It is not an easy decision on HIV, especially in Zambia": opting for silence, limited disclosure and implicit understanding to retain a wider identity
    Bond, Virginia Anne
    [J]. AIDS CARE-PSYCHOLOGICAL AND SOCIO-MEDICAL ASPECTS OF AIDS/HIV, 2010, 22 : 6 - 13
  • [8] ''I don't want financial support but verbal support.'' How do caregivers manage children's access to and retention in HIV care in urban Zimbabwe?
    Busza, Joanna
    Dauya, Ethel
    Bandason, Tsitsi
    Mujuru, Hilda
    Ferrand, Rashida A.
    [J]. JOURNAL OF THE INTERNATIONAL AIDS SOCIETY, 2014, 17
  • [9] "I have grown up controlling myself a lot." Fear and misconceptions about sex among adolescents vertically-infected with HIV in Tanzania
    Busza, Joanna
    Besana, Giulia V. R.
    Mapunda, Pasiens
    Oliveras, Elizabeth
    [J]. REPRODUCTIVE HEALTH MATTERS, 2013, 21 (41) : 87 - 96
  • [10] Butler-Kisber L, 2010, J RES PRACT, V6