Resources

Miller, L. M., Whitlatch, C. J., Lee, C. S., & Lyons, K. S. (2018). Incongruent perceptions of the care values of hospitalized person with dementia: A pilot study of patient-family caregiver dyads. Aging & Mental Health, 22(4), 489-496. doi:10.1080/13607863.2017.1280766

Castora-Binkley, M., Noelker, L. S., Ejaz, F. K., & Rose, M. (2011). Inclusion of caregiver supports and services in home- and community-based service programs: Recent reports from state units on aging. Journal of Aging & Social Policy, 23(1), 19-33. doi:10.1080/08959420.2011.532001

Whitlatch, C. J. (2001). Including the person with dementia in family care-giving research. Aging & Mental Health, 5(Suppl.1), S20-S22. doi:10.1080/713650016

Judge, K. S., Yarry, S. J., Looman, W. J., & Bass, D. M. (2013). Improved strain and psychosocial outcomes for caregivers of individuals with dementia: Findings from Project ANSWERS. The Gerontologist, 53(2), 280-292. doi:10.1093/geront/gns076

Noelker, L. S. & Harel, Z. (2000). Humanizing long-term care: Forging a link between quality of care and quality of life. In L. S. Noelker, & Z. Harel (Eds.), Linking quality of long-term care and quality of life (pp. 3-26). New York, NY: Springer.