Resource Library

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.

Looman, W. J., Noelker, L. S., Schur, D., Whitlatch, C. J. & Ejaz, F. K. (2002). Impact of family members on nurse assistants: What helps, what hurts. American Journal of Alzheimer's Disease and Other Dementias, 17(6), 350-356. doi:10.1177/153331750201700606

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.

Menne, H. L., Ejaz, F. K., Noelker, L. S., & Jones, J. A. (2007). Direct care workers' recommendations for training and continuing education. Gerontology & Geriatrics Education, 28(2), 91-108. doi:10.1300/J021v28n02_07

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