Resource Library

Whitlatch, C. J. & Feinberg, L. F. (2006). Family and friends as respite providers. Journal of Aging & Social Policy, 18(3-4), 127-139. doi:10.1300/J031v18n03_09

Bass, D. M., Noelker, L. S., & McCarthy, C. A. (1999). The influence of formal and informal helpers on primary caregivers' perceptions of quality of care. Journal of Applied Gerontology, 18(2), 177-200. doi:10.1177/073346489901800204

Shelton, E. G., Orsulic-Jeras, S., Whitlatch, C. J., & Szabo, S. M. (2018). Does it matter if we disagree? The impact of incongruent care preferences on persons with dementia and their care partners. The Gerontologist, 58(3), 556-566. doi:10.1093/geront/gnw202

Piiparinen, R., & Whitlatch, C. J. (2011). Existential loss as a determinant to well-being in the dementia caregiving dyad: A conceptual model. Dementia, 10(2), 185-201.

Sebern, M. D., Sulemanjee, N., Sebern, M. J., Garnier-Villarreal, M., & Whitlatch, C. J. (2017). Does an intervention designed to improve self-management, social support and awareness of palliative-care address needs of persons with heart failure, family caregivers and clinicians? Journal of Clinical Nursing, 27(3-4), e643-e657. doi:10.1111/jocn.14115.