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AIDS Care
Psychological and Socio-medical Aspects of AIDS/HIV
Volume 7, 1995 - Issue 2
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Original Articles

Carers' burden and adjustment to HIV

Pages 189-204 | Published online: 27 May 2010

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

Read on this site (13)

Zamri Hassan. (2016) Stigma reduction initiatives: caregivers of multi faces. Asia Pacific Journal of Social Work and Development 26:2-3, pages 152-166.
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NO Ama & ES Seloilwe. (2011) Analysis of the burdens of caregivers providing care to people living with HIV/AIDS in Botswana. South African Family Practice 53:1, pages 56-62.
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Tania Basta, Enbal Shacham & Michael Reece. (2008) Psychological distress and engagement in HIV-related services among individuals seeking mental health care. AIDS Care 20:8, pages 969-976.
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Alyssa J. Averill, Edward J. Kasarskis & Suzanne C. Segerstrom. (2007) Psychological health in patients with amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis 8:4, pages 243-254.
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S. Cadell. (2003) Trauma and growth in Canadian carers. AIDS Care 15:5, pages 639-648.
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Cynthia Cannon Poindexter. (2002) “Twists and Turns”. Journal of HIV/AIDS & Social Services 1:1, pages 113-135.
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Kenneth Pakenham & Machelle Rinaldis. (2002) Development of the HIV/AIDS Stress Scale. Psychology & Health 17:2, pages 203-219.
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Tomas Campbell. (1999) AIDS-related death: A review of how bereaved gay men are affected. Counselling Psychology Quarterly 12:3, pages 245-252.
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Articles from other publishers (21)

Kenneth I. Pakenham & Christina Samios. (2012) Couples coping with multiple sclerosis: a dyadic perspective on the roles of mindfulness and acceptance. Journal of Behavioral Medicine 36:4, pages 389-400.
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Stuart Wright, Flavia Zalwango, Janet Seeley, Joseph Mugisha & Francien Scholten. (2012) Despondency Among HIV-Positive Older Men and Women in Uganda. Journal of Cross-Cultural Gerontology 27:4, pages 319-333.
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W. Punpanich, P. M. Gorbach & R. Detels. (2011) Impact of paediatric human immunodeficiency virus infection on children's and caregivers' daily functioning and well‐being: a qualitative study. Child: Care, Health and Development 38:5, pages 714-722.
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Ian MunroKaren-Leigh Edward. (2009) The Burden of Care of Gay Male Carers Caring for Men Living With HIV/AIDS. American Journal of Men's Health 4:4, pages 287-296.
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Olagoke Akintola. (2008) Defying all odds: coping with the challenges of volunteer caregiving for patients with AIDS in South Africa. Journal of Advanced Nursing 63:4, pages 357-365.
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K.I. Pakenham. (2007) The nature of caregiving in multiple sclerosis: development of the caregiving tasks in multiple sclerosis scale. Multiple Sclerosis Journal 13:7, pages 929-938.
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Michael D. Stein, Debra S. Herman, Duane Bishop, Bradley J. Anderson, Elizabeth Trisvan, Rosalie Lopez, Timothy Flanigan & Ivan Miller. (2006) A Telephone-Based Intervention for Depression in HIV Patients: Negative Results from a Randomized Clinical Trial. AIDS and Behavior 11:1, pages 15-23.
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Patricia Engler, Bradley Anderson, Debra Herman, Duane Bishop, Ivan Miller, Paul Pirraglia, Jumi Hayaki & Michael Stein. (2006) Coping and Burden Among Informal HIV Caregivers. Psychosomatic Medicine 68:6, pages 985-992.
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Kenneth I Pakenham & Samantha Bursnall. (2016) Relations between social support, appraisal and coping and both positive and negative outcomes for children of a parent with multiple sclerosis and comparisons with children of healthy parents. Clinical Rehabilitation 20:8, pages 709-723.
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Debra S. Herman, Duane Bishop, Jennifer L. Anthony, William Chase, Elizabeth Trisvan, Rosalie Lopez & Michael D. Stein. (2006) Feasibility of a Telephone Intervention for HIV Patients and Their Informal Caregivers. Journal of Clinical Psychology in Medical Settings 13:1, pages 78-88.
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E. Robson, N. Ansell, U. S. Huber, W. T. S. Gould & L. van Blerk. (2006) Young caregivers in the context of the HIV/AIDS pandemic in sub‐Saharan Africa. Population, Space and Place 12:2, pages 93-111.
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Kenneth I. Pakenham. (2005) Relations Between Coping and Positive and Negative Outcomes in Carers of Persons with Multiple Sclerosis (MS). Journal of Clinical Psychology in Medical Settings 12:1, pages 25-38.
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Pimpaporn Klunklin & Rosanne C. Harrigan. (2002) Child-rearing practices of primary caregivers of HIV-infected children: An integrative review of the literature. Journal of Pediatric Nursing 17:4, pages 289-296.
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Helen Land & Sharon Hudson. (2002) HIV serostatus and factors related to physical and mental well-being in Latina family AIDS caregivers. Social Science & Medicine 54:1, pages 147-159.
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Jacquelyn H. Flaskerud & Patricia Lee. (2008) Vulnerability to health problems in female informal caregivers of persons with HIV/AIDS and age‐related dementias. Journal of Advanced Nursing 33:1, pages 60-68.
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Judith G. Rabkin, Glenn J. Wagner & Maura Del Bene. (2000) Resilience and Distress Among Amyotrophic Lateral Sclerosis Patients and Caregivers. Psychosomatic Medicine 62:2, pages 271-279.
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JEAN MEADOWS, KATHRYN LE MARÉCHAL & JOSE CATALÁN. (1999) The Burden of Care: The Impact of HIV-Associated Dementia on Caregivers. AIDS Patient Care and STDs 13:1, pages 47-56.
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Kenneth I Pakenham. (1998) Specification of social support behaviours and network dimensions along the HIV continuum for gay men. Patient Education and Counseling 34:2, pages 147-157.
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Laurel C. Beery, Holly G. Prigerson, Andrew J. Bierhals, Lisa M. Santucci, Jason T. Newsom, Paul K. MacIejewski, Stephen R. Rapp, Amy Fasiczka & Charles F. ReynoldsIIIIII. (2016) Traumatic Grief, Depression and Caregiving in Elderly Spouses of the Terminally Ill. OMEGA - Journal of Death and Dying 35:3, pages 261-279.
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Mary Ann Hoffman. (1997) HIV Disease and Work: Effect on the Individual, Workplace, and Interpersonal Contexts. Journal of Vocational Behavior 51:2, pages 163-201.
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Barbara G. Melamed. (1995) Psychological aspects of AIDS. Current Opinion in Psychiatry 8:6, pages 414-418.
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