Abstract

 


 



Bioethics and Cancer: When the Professional Becomes Personal


Rebecca Dresser, JD


Washington University in Saint Louis - School of Law

May 29, 2012

HASTINGS CENTER REPORT, Nov.-Dec. 2011, at 14-18

Abstract:     
Scholars in bioethics and health policy often address topics related to cancer, yet few engaged in this work have lived with cancer themselves. Experience as a cancer patient or family caregiver extends and deepens one’s thinking about issues in ethics and health policy. This essay presents material from a project involving seven scholars who have been cancer patients or cared for a spouse with cancer. It describes how personal experience changed and supplemented our understanding of topics like treatment decision-making, patient autonomy, informed consent, and end-of-life care. The essay calls on scholars to give more consideration to the lived experience of illness when analyzing issues in bioethics and health policy.

Keywords: bioethics, cancer patients, family caregiving, treatment decision-making, informed consent, end-of-life care

Accepted Paper Series


Date posted: May 30, 2012  

Suggested Citation

Dresser, JD, Rebecca, Bioethics and Cancer: When the Professional Becomes Personal (May 29, 2012). HASTINGS CENTER REPORT, Nov.-Dec. 2011, at 14-18. Available at SSRN: http://ssrn.com/abstract=2070030

Contact Information

Rebecca Dresser, JD (Contact Author)
Washington University in Saint Louis - School of Law ( email )
Campus Box 1120
St. Louis, MO 63130
United States
Feedback to SSRN (Beta)


Paper statistics
Abstract Views: 176

© 2013 Social Science Electronic Publishing, Inc. All Rights Reserved.  FAQ   Terms of Use   Privacy Policy   Copyright
This page was processed by apollo5 in 0.407 seconds