Promoting consumer direction for family caregiver support: An agency-driven model

Generations

Volumn 24, Issue 3, 2000, Pages 47-53

  Feinberg, Lynn Friss ^a   Ellano, Claudia ^b,c  

^a Family Caregiver Alliance   (United States)

^b ST JUDE MEDICAL CENTER   (United States)

^c CALIFORNIA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0041034346     PISSN: 07387806     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (16)

1. Baxter, E. 1997. "Patients, Caregivers and Managing Care." Geriatrics 52 (suppl. 2), 548-49.
2. Boise, L., Heagerty, B., and Eskenazi, L. 1996. "Facing Chronic Illness: The Family Support Model and Its Benefits." Patient Education and Counseling 27: 75-84.
3. Ellano, C. December 1997. "Caregiver Resource Centers Revised Assessment Tool Training." Presentation to clinical staff. San Francisco.
4. Feinberg, L. F., and Kelly, K. A. 1995. "A Well-Deserved Break: Respite Options Offered by California's Statewide System of Caregiver Resource Centers." Gerontologist 35: 701-5.
5. Feinberg, L. F., and Whitlatch, C. J. 1998. "Family Caregivers and In-Home Respite Options: The Consumer-Directed versus Agency-Based Experience." Journal of Gerontological Social Work 30(3/4): 9-28.
6. Feinberg, L. F., Whitlatch, C. J., and Tucke, S. 2000. Making Hard Choices: Respecting Both Voices. Final Report to The Robert Wood Johnson Foundation. San Francisco: Family Caregiver Alliance.
7. Friss, L. R. 1993. "Family Caregivers as Case Managers: A Statewide Model for Enhancing Consumer Choice? Journal of Case Management 2: 53-8.
8. Friss., L. 1990. "A Model State-Level Approach to Family Survival for Caregivers of Brain-Impaired Adults." Gerontologist 30: 121-5.
9. Greene, R., and Feinberg, L. F. 1999. "State Initiatives for Caregivers of People with Dementia." Generations 23: 75-77.
10. Haynie, D., Feinberg, L. F., and Zarit, S. H. 2000. Community Service Outcomes for Caregivers of Cognitively Impaired Adults: Preliminary Report. San Francisco: Family Caregiver Alliance.
11. Institute for the Future. 2000. Health and Health Care 2010: The Forecast, The Challenge. San Francisco: Jossey-Bass.
12. Kane, R. A., and Degenholtz, H. 1997. "Assessing Values and Preferences: Should We, Can We?" Generations 21(1): 19-24.
13. Kelly, K. A., Farrell, V., and Johnson, P. 2000. "Link2Care: An Internet-Based Information and Support Program for Family Caregivers." Presented at the 46th Annual Meeting of the American Society on Aging, San Diego, Calif.
14. Levine, C. and Zuckerman, C. 1999. "The Trouble with Families: Toward an Ethic of Accommodation." Annals of Internal Medicine 130: 148-52.
15. Linsk, N. L., et al. 1988. "Community Agency Support of Family Caregiving." Health and Social Work (Summer): 209-18.
16. Winslow, W.B. 1997. "Effects of Formal Supports on Stress Outcomes in Family Caregivers of Alzheimer's Patients." Research in Nursing and Health 20: 27-37.