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AIDS Care
Psychological and Socio-medical Aspects of AIDS/HIV
Volume 5, 1993 - Issue 1
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Editorial

The family and HIV disease

Pages 3-4 | Published online: 25 Sep 2007

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (3)

Premilla D’Cruz. (2008) The healthcare system in HIV/AIDS: an inextricable component in the experience of family care. Critical Public Health 18:2, pages 189-209.
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ILSE PAUW & LOREN BRENER. (1998) Naming the dangers of working on the street. Agenda 13:36, pages 80-83.
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David Nord. (1996) The impact of multiple aids-related loss on families of origin and families of choice. The American Journal of Family Therapy 24:2, pages 129-144.
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Articles from other publishers (6)

Premilla D’CruzBhupinder Arora. (2010) The Interface between the Family and the Health Care System in the Care of People with HIV/AIDS. Journal of Health Management 12:3, pages 273-304.
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Catherine A. O'Connor, Sally K. Fauchald, Carol A. Patsdaughter, Cecelia Gatson Grindel & Maria Susana Medeiros. (2004) Remembering Those Who Have Gone Before: The Importance of AIDS Memorial Services for Families and Friends. Illness, Crisis & Loss 12:4, pages 307-318.
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Rebecca Spirig. (2016) In Invisibility and Isolation: The Experience of HIV-Affected Families in German-Speaking Switzerland. Qualitative Health Research 12:10, pages 1323-1337.
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Premilla D'Cruz. (2018) Engulfing Darkness: The Impact of HIV/AIDS on the Family. Families in Society: The Journal of Contemporary Social Services 83:4, pages 416-430.
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Caroline Carlisle. (2016) The Search for Meaning in HIV and AIDS: The Carers’ Experience. Qualitative Health Research 10:6, pages 750-765.
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Marie‐Annette Brown. (2007) Knowledge Generation for the HIV‐Affected Family. Image: the Journal of Nursing Scholarship 29:3, pages 269-274.
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