African American female caregivers of family members living with HIV/AIDS

Families in Society

Volumn 82, Issue 2, 2001, Pages 145-156

  Tolliver, Derise E ^a  

^a DEPAUL UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0035289547     PISSN: 10443894     EISSN: None     Source Type: Journal    
DOI: 10.1606/1044-3894.215     Document Type: Article

References (40)

1. Akbar, N. (1991). The evolution of human psychology for African Americans. In R. Jones (Ed.), Black psychology. Third Edition. Berkeley, CA: Cobb & Henry.
2. Baker, S., Sudit, M. & Litwak, E. (May-June, 1998). Caregiver burden and coping strategies used by informal caregivers of minority women living with HIV/AIDS. ABNF Journal, 56-60.
3. Biegel D.E., Sales, E. & Schulz, R. (1991). Family caregiving in chronic illness: Alzheimer's disease, cancer, heart disease, mental illness, and stroke. Newbury Park, CA: Sage.
4. Boyd-Franklin, N., Aleman, J. C., Jean-Gilles, M. M. & Lewis, S. Y. (1995). Cultural sensitvity and competence: African-American, Latino and Haitian families with HIV/AIDS. In Children, families and HIV/AIDS. N. Boyd-Franklin, G. L. Steiner & M. G. Bolan, (Eds.). New York: Guilford Press, 53-77.
5. Boyle, J. S., Ferrell, J. A., Hodincki, D. R. & Muller, R. B. (1997). Going home: African-American caregiving for adult children with human immunodefiency virus disease. Holistic Nursing Practice, 11, 27-35.
6. Brennan, P. F. & Moore, S. M. (1994). Caregivers of persons living with AIDS. In E. Kahana, D. Biegel, & M. Wykie (Eds.). Family caregiving across the lifespan. Newbury Park, CA: Sage.
7. Brown, D. R. (1997). Cultural mistrust among African-Americans: Results from Cancer Awareness & Behavior Survey. Detroit, MI: Center for Urban Studies, Wayne State University.
8. Brown, D. R. & Sankar, A. (1998). HIV/AIDS and aging minority populations. Research on Aging, 20, 865-885.
9. Brown, M.A. (1994). Family caregiving in HIV infection: Current knowledge development and a vision for the future. American Academy of Nursing, HIV/AIDS Nursing Care Summit Proceedings, Washington, DC.
10. Brown, M. A. & Powell-Cope, G. M. (1991). AIDS family caregiving: Transitions through uncertainty. Nursing Research, 40, 338-345.
11. Crawford, A. M. (1996). Stigma associated with AIDS: A metaanalysis. Journal of Applied Social Psychology, 26, 398-416.
12. Duh, S. (1991). Blacks and AIDS. Newbury Park, CA: Sage.
13. Flaskerud, J. H. & Tabora, B. (1998). Health problems of low-income female caregivers of adults with HIV/AIDS. Health Care for Women International, 19, 23-36.
14. Folkman, S., Chesney, M. A., & Christopher-Richards, A. (1994). Stress and coping in caregiving partners of men with AIDS. Psychiatric Clinics of North America, 17, 35-53.
15. Hackl, K. L., Somlai, A. M., Kelly, J. A., & Kalichman, S. C. (1997). Women living with HIV/AIDS: The dual challenge of being a patient and caregiver. Health & Social Work, 22, 53-62.
16. Kubler-Ross, E. (1987). AIDS: the ultimate challenge. New York: Macmillan.
17. McCann, K. & Wadsworth, E. (1992). The role of informal carers in supporting gay men who have HIV related illness: what do they do and what are their needs? AIDS Care, 4, 25-34.
18. Mindel, C. H. & Wright, R. (1982). The use of social services by Black and White elderly: The role of social support systems. Journal of Gerontological Social Work, 3(3-4), 107-125.
19. Mui, A. C. (1992). Caregiver strain among Black and White daughter caregivers: A role theory perspective. The Gerontologist, 32, 203-212.
20. Mullan, J.T. (1998). Aging and informal caregiving to people with HIV/AIDS. Research on Aging, 20, 712-738.
21. Myers, L. J. (1991). Expanding the psychology of knowledge optimally: The importance of world view revisited. In R. Jones (Ed.). Black psychology, (3rd ed.). Berkeley, CA: Cobb & Henry, 15-32.
22. Nobles, W. W. (1991). African philosophy: Foundations of Black psychology. In R. Jones (Ed.). Black psychology: Third Edition. Berkeley, CA: Cobb & Henry Publishers, 47-65.
23. Patton, M. Q. (1990). Qualitative evaluation and reserarch methods. Newbury Park: Sage.
24. Pearlin., L. I., Aneshensel, C. S., & LeBlanc, A. J. (1997). The forms and mechanisms of stress proliferation: The case of AIDS caregivers. Journal of Health & Social Behavior, 38, 223-236.
25. Pearlin, L. I. & Mullan, J. (1994). The structure of functions of AIDS caregiving relationships. Psychosocial Rehabilitation Journal, 17(4), 51-68.
26. Poindexter, C. C. & Linsk, N. L. (1999). HIV-related stigma in a sample of HIV-affected older female African American caregivers. Social Work, 44, 46-61.
27. Poindexter, C. C. & Linsk, N. L. (1998). Sources of support in a sample of HIV-affected older minority caregivers. Families in Society, 79, 497-503.
28. Powell-Cope & Brown, M. A. (1992). Going public as an AIDS family caregiver. Social Science and Medicine, 34, 571-580.
29. Raveis, V. & Siegel, K. (1991, February). Impact of caregiving on informal or familial caregivers. AIDS Patient Care, 39-43.
30. Reynold, N. R. & Alonzo, A. A. (1998). HIV informal caregiving: Emergent conflict and growth. Research in Nursing & Health, 21, 251-260.
31. Rinelle, V. J. & Dubin, W. R. (1988). The hidden victims of AIDS: Healthcare workers and families. Psychiatric Hospital, 19, 115-120.
32. Rodgers-Rose, L. E. (1980). The Black woman: A historical overview. In L. F. Rodgers-Rose (Ed.). The Black woman. Beverly Hill, CA: Sage.
33. Rodrigues-Trias, H. & Marte, C. (1995). Challenges and possibilities: Women, HIV and the health care system in the 1990's. In B. E. Schneider & N. E. Stoller. Women resisting AIDS. Philadelphia, PA: Temple University Press, 301-322.
34. Rutman, D. (1996). Caregiving as women's work: Women's experiences of powerfulness and powerlessness as caregivers. Qualitative Health Research, 6, 90-112.
35. Schiller, N.G. (1993). The invisible women: caregiving and the construction of AIDS health services. Culture, Medicine, and Psychiatry, 17, 487-512.
36. Trice, A.D. (1988). Posttraumatic stress syndrome-like symptoms among AIDS caregivers. Psychological Reports, 63, 656-658.
37. Turner, H. & Catania, J. (1997). Informal caregiving to persons with AIDS in the United States: Caregiver burden among central cities residents eighteen to forty-nine years old. American Journal of Community Psychology. 25, 35-59.
38. Turner, H., Catania, J.A. & Gagnon, J. (1994). The prevalence of informal caregiver to persons with AIDS in the United States: Caregiver characteristics and their implications. Social Science and Medicine, 38, 1548-1552.
39. Wardlaw, L. (1994). Sustaining informal caregivers for persons with AIDS. Families in Society, 75, 373-384.
40. Wykle, M. & Segal, M. (1989). A comparison of Black and White family caregivers experience with dementia. Journal of the National Black Nurses Association, 29-41.