The  Disability Ethics Initiative

 
 

The disability ethics initiative was established in 1999 to promote an examination of values and ethics that affect our social understanding of and our response to disability. The goals of the initiative are: (1) to encourage productive dialogue between disability ethicists and other ethicists; (2) to ensure the perspectives of people with disabilities are adequately considered in ethical healthcare delivery, and (3) to encourage holistic approaches to disability ethics that are not constrained by traditional boundaries of health, medical. or bioethics.

 
Related Projects & Materials
What sorts of people should there be? (opens in a new window) This University of Alberta based project studies the attempts to establish membership requirements for the human race from historical attempts at eugenics to cutting-edge biotechologies and bioethics.

VP-Net End of Life Care Project This University of Manitoba based project, sponsored by the Canadian Institute for Health Research explores end-of-life options for vulnerable people.

The Newsletter of The Network on Ethics and Intellectual Disabilities (opens in a new window) Published by the Kennedy Institute on Ethics at Georgetown University. For more information on the Network or to download issues of the newsletter.http://www.whatsorts.net/http://www.whatsorts.net/http://kennedyinstitute.georgetown.edu/publications/network_on_ethics.htmhttp://kennedyinstitute.georgetown.edu/publications/network_on_ethics.htmhttp://kennedyinstitute.georgetown.edu/publications/network_on_ethics.htmshapeimage_2_link_0shapeimage_2_link_1shapeimage_2_link_2shapeimage_2_link_3shapeimage_2_link_4

About the Initiative

Who  is driving the agenda and where are we headed?

Defining Disability Ethics

Defining Disability Ethics is a Research Development Initiative funded by The Social Sciences and Research Council of Canada from 2008 to 2010. For More information, visit the Defining Disability Ethics Project Page.