The Positive aspects of the caregiving journey with dementia: Using a strengths-based perspective to reveal opportunities

Journal of Applied Gerontology

Volumn 29, Issue 5, 2010, Pages 640-659

  Peacock, Shelley ^a   Forbes, Dorothy ^b   Markle Reid, Maureen ^c   Hawranik, Pamela ^d   Morgan, Debra ^e   Jansen, Lynn ^b   Leipert, Beverly D ^c   Henderson, Sandra R ^c  

^a UNIVERSITY OF ALBERTA   (Canada)

^b UNIVERSITY OF WESTERN ONTARIO   (Canada)

^c MCMASTER UNIVERSITY   (Canada)

^d ATHABASCA UNIVERSITY   (Canada)

^e UNIVERSITY OF SASKATCHEWAN   (Canada)

Author keywords

Dementia; Family caregivers; Positive aspects

Indexed keywords

ADULT; AGED; ARTICLE; CAREGIVER; CLINICAL ARTICLE; COMPETENCE; DEMENTIA; FAMILY CENTERED CARE; FEMALE; HEALTH CARE QUALITY; HUMAN; INTERVIEW; MALE; QUALITATIVE ANALYSIS; SECONDARY ANALYSIS; SOCIAL SUPPORT;

EID: 78650605614     PISSN: 07334648     EISSN: 15524523     Source Type: Journal    
DOI: 10.1177/0733464809341471     Document Type: Article

References (33)

1. Andren, S., &Elmstahl, S. (2005). Family caregiverś subjective experiences of satisfaction in dementia care: Aspects of burden, subjective health and sense of coherence. Scandinavian Journal of Caring Science, 19, 157-168. (Pubitemid 41602998)
2. Ayres, L. (2000). Narratives of family caregiving: The process of making meaning. Research in Nursing &Health, 23, 424-434.
3. Berg-Weger, M., Rubio, D. M., &Tebb, S. (2001). Strengths-based practice with family caregivers of the chronically ill: Qualitative insights. Families in Society: Journal of Contemporary Human Services, 82, 263-272.
4. Buhr, G., Kuchibhatla, M., &Clipp, E. (2006). Caregiverś reasons for nursing home placement: Clues for improving discussions with families prior to the transition. The Gerontologist, 46, 52-61. (Pubitemid 43214415)
5. Butcher, H., Holkup, P., &Buckwalter, K. (2001). The experience of caring for a family member with Alzheimer's disease. Western Journal of Nursing Research, 23, 33-55. (Pubitemid 33610468)
6. Canadian Study of Health and Aging Working Group. (1994). Patterns of caring for people with dementia in Canada. Canadian Journal on Aging, 13, 470-487.
7. Canadian Study of Health and Aging Working Group. (2000). The incidence of dementia in Canada. Neurology, 55, 66-73.
8. Carruth, A. (1996). Motivating factors, exchange patterns, and reciprocity among caregivers of parents with and without dementia. Research in Nursing and Health, 19, 409-419. (Pubitemid 126702594)
9. Cohen, C., Colantonio, A., &Vernich, L. (2002). Positive aspects of caregiving: Rounding out the caregiving experience. International Journal of Geriatric Psychiatry, 17, 184-188. (Pubitemid 34130311)
10. Decima Research for Health Canada, Decima Research for Health Canada. (2002). National profile of family caregivers in Canada-2002: Final report. Prepared for Health Canada, Ottawa, ON: Decima Research Incorporated.
11. Ejaz, F., Noelker, L., Schur, D., Whitlach, C., &Looman, W. (2002). Family satisfaction with nursing home care for relatives with dementia. Journal of Applied Gerontology, 21, 368-384.
12. Farran, C. (1997). Theoretical perspectives concerning positive aspects of caring for elderly persons with dementia: Stress/adaptation and existentialism. The Gerontologist, 37, 250-256. (Pubitemid 27181282)
13. Fast, J. (2005). Caregiving: A fact of life. Transition Magazine, 35(2). Retrieved February 6, 2006, from http://www.vifamily.ca/library/transition/352/ 352.html
14. Fast, J., Keating, N., Otfinowski, P., &Derksen, L. (2003). Characteristics of family/ friend care networks of frail seniors. Canadian Journal on Aging, 23, 5-19.
15. Fast, J., Niehaus, L., Eales, J., &Keating, N. (2002). A profile of Canadian palliative care providers. Research on aging, policies and practice. Final report submitted to Human Resources and Development Canada, Department of Human Ecology, University of Alberta, Edmonton, Canada.
16. Forbes, D., Jansen, L., Markle-Reid, M., Hawranik, P., Morgan, D., Henderson, S., et al. of home- and community-based health services. Canadian Journal of Nursing Research, 40, 38-59.
17. Forbes, D., Markle-Reid, M., Hawranik, P., Peacock, S., Kingston, D., Morgan, D., et al. (2008). Availability and acceptability of Canadian home and communitybased services: Perspectives of family caregivers of persons with dementia. Home Health Care Services Quarterly, 27, 75-99.
18. Forbes, D., &Neufeld, A. (2008). Looming dementia care crisis: Canada needs an integrated model of continuing care now! Canadian Journal of Nursing Research, 40(1), 9-16.
19. Gottlieb, B., &Rooney, J. (2004). Coping effectiveness: Determinants and relevance to the mental health and affect of family caregivers of persons with dementia. Aging & Mental Health, 8, 364-373. (Pubitemid 38954357)
20. Graybeal, C. (2001). Strengths-based social work assessment: Transforming the dominant paradigm. Families in Society: Journal of Contemporary Human Services, 82, 233-242.
21. Keating, N., Fast, J., Frederick, J., Cranswick, K., &Perrier, C. (1999). Eldercare in Canada: Context, content and consequences. Ottawa, ON: Statistics Canada.
22. Kellett, U. (2007). Seizing possibilities for positive family caregiving in nursing homes. Journal of Clinical Nursing, 16, 1479-1487.
23. Kelley, L. S., Specht, J. K., &Maas, M. (2000). Family involvement in care for individuals with dementia protocol. Journal of Gerontological Nursing, 26, 13-21.
24. Louderback, P. (2000). What's happening: Elder care: A positive approach. Journal of the American Academy of Nurse Practitioners, 12, 97-99.
25. Neufeld, A., &Harrison, M. (1998). Men as caregivers: Reciprocal relationships or obligation? Journal of Advanced Nursing, 28, 959-968. (Pubitemid 128451586)
26. Rapp, C. (1998). The strengths model: Case management for people suffering from severe and persistent mental illness. New York: Oxford University Press.
27. Saleebey, D. (2009). Introduction: Power in the people. In D. Saleebey (Ed.), The strengths perspective in social work practice (5th ed., pp. 1-23). New York: Pearson.
28. Sanders, S. (2005). Is the glass half empty or half full? Reflections on strain and gain in caregivers of individuals with Alzheimer's disease. Social Work in Health Care, 40, 57-73.
29. Schulz, R., &Martire, L. (2004). Family caregiving of persons with dementia. American Journal of Geriatric Psychiatry, 12, 240-249.
30. Silverstein, M., Conroy, S., Wang, H., Giarrusso, R., &Bengston, V. (2002). Reciprocity in parent-child relations over the adult life course. Journal of Gerontology: Social Sciences, 57B(1), S3-S13. (Pubitemid 34052891)
31. Specht, J. P., Kelley, L., Manion, P., Mass, M., Reed, D., &Rantz, M. (2000). Who's the Boss? Family/staff partnership in care of persons with dementia. Nursing Administration Quarterly, 24, 64-77.
32. Thorne, S., Reimer Kirkham, S., &MacDonald-Emes, J. (1997). Focus on qualitative methods interpretive description: A noncategorical qualitative alternative for developing nursing knowledge. Research in Nursing &Health, 20, 168-177.
33. Thorne, S., Reimer Kirkham, S., &O'Flynn-Magee, K. (2004). The analytic challenge in interpretive description. International Journal of Qualitative Methods, 3, 1-21.