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Content with Topic Family Caregiving times .

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Whitlatch, C. J. (1998). Distress and burden for family caregivers. In A. Wimo, B. Jonsson, G. Karlsson, & B. Winblad (Eds.), Health Economics of Dementia (pp. 123-137). London: John Wiley & Sons, Ltd.

Weitzman, L. (2019, May 15). How to Avoid Letting Caregiving Lead to Emotional Eating. Retrieved from https://www.guideposts.org/caregiving/resource-center/how-to-avoid-letting-caregiving-lead-to-emotional-eating.

Bass, D. M., McCarthy, C., Eckert, S., & Bichler, J. (1994). Differences in service attitudes and experiences among families using three types of support services. The American Journal of Alzheimer's Care and Related Disorders & Research, 9(3), 28-38. doi:10.1177/153331759400900306

Nagpal, N., Heid, A. R., Zarit, S. H., & Whitlatch, C. J. (2015). Religiosity and quality of life: A dyadic perspective of individuals with dementia and their caregivers. Aging & Mental Health, 19(6), 500-506. doi:10.1080/13607863.2014.952708

Bass, D. M., McClendon, M. J., Brennan, P. F., & McCarthy, C. (1998). The buffering effect of a computer support network on caregiver strain. Journal of Aging and Health, 10(1), 20-43. doi:10.1177/089826439801000102