Abstract
In almost every way, cancer care in the United States today reflects brilliant advances in research, education, and training. Patients receive sophisticated treatments that have become so routine family members can provide them at home. When they want to be involved in treatment decisions, these same patients and families can turn to the Internet and learn about clinical trials and recommendations from the best medical facilities throughout the world. As patients receive chemotherapy and other treatments at home, medical professionals are turning over care to families and other nonprofessional caregivers. However, while cancer diagnosis and treatment explode with promise for the future, policies that support families providing care lag far behind.
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Kaufman, D.L., O’Mara, A., Schrauf, C.M. (2012). Cancer Caregiving: Policy and Advocacy. In: Talley, R., McCorkle, R., Baile, W. (eds) Cancer Caregiving in the United States. Caregiving: Research • Practice • Policy. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-3154-1_14
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