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Edwards, S. (2018). Reducing the financial fatigue of caregiving. IMPACT on Wellness, 2.

Weitzman, L. (2018). The stigma around caregiving. IMPACT on Wellness, 2.

Bass, D. M., Judge, K. S., Snow, L.A., Wilson, N. L., Morgan, R., Looman, W. J., McCarthy, C. A., Maslow, K., Moye, J. A., Randazzo, R., Garcia-Maldonado, M., Elbein, R., Odenheimer, G., & Kunik, M. E. (2013). Caregiver outcomes of Partners in Dementia Care: Effect of a care coordination program for veterans with dementia and their family members and friends. Journal of the American Geriatrics Society, 61(8), 1377-86.

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Bass, D.M., Judge, K.S., Snow, L.A., Wilson, N.L., Looman, W.J., McCarthy, C.A., Morgan, R., & Abloorh-Odjidja, C., Kunik, M.E. (2012). Prevalence and predictors of depression, care-related strain, and unmet needs among caregivers of patients with dementia. The American Journal of Geriatric Psychiatry, 20, 239-247.

Bass D.M., Easom, L., Primetica, B., & Holloway, C.J. (2015). Reflections on implementing the evidence-based BRI Care Consultation with RCI in Georgia. Generations, Journal of the American Society on Aging, 39(4), 49-56.

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