This blog is the combined effort of a team of researchers and community members working around the world in different disciplines to address concerns around human variation, normalcy, and enhancement. This blog is a place for academics, community members and individuals alike to connect, find information and discuss issues related to the What Sorts? project.
A movie review site lets you know how easy reviewed films are to watch by the visually impaired. In my home town (Toronto) the Edge radio station had a blind movie reviewer who was featured on the morning show. I think it was supposed to be tongue in cheek but the reviewer was really intelligent and witty, and he did report back on how easy it was to figure out what was going on.
This post kicks off a series of posts at What Sorts that we hope will appear every Tuesday and Friday over the next few months called Thinking in Action. In the first instance, this series will offer commentaries on talks and discussions at the recent conference Cognitive Disability: A Challenge to Moral Philosophy. The aims of these Thinking in Action posts will be to generate and advance discussion of specific issues that arise in taking up the themes of the conference. The posts will typically feature a relatively short clip from a talk or discussion at the conference, followed by a commentary; transcripts of all excerpted video clips will appear at the end of each post. In light of our experience with this first (extended) round of posts, we’ll see whether we continue the series with clusters of posts with other thematic focuses. We will both tag and categorize each post with the series label “Thinking in Action” so that you can review them together, if you like, and we encourage the use of posts in the series in classrooms, in local discussion groups, and in organizations at the interface of government, university, and community. We will aim to make each of these self-contained, with the conference podcasts themselves serving as a larger reservoir of perspectives on cognitive disability on which you can draw. We hope that you will join in the discussions, both on the blog and beyond it.
To help us get some idea of what readers know about the conference podcasts we’ll be discussing, here’s a quick poll that we encourage you to take before proceeding.
As one might expect, Peter Singer’s talk at the conference Cognitive Disability: A Challenge to Moral Philosophy, presents ideas that Singer is well-known for. Amongst these are views that draw parallels between animals, on the one hand, and individuals with disabilities, on the other, especially those with “profound mental retardation”, a medical category that includes, amongst other features, having an IQ of 25 or below. I want to kick off this series of blog posts not with a discussion of that general comparison—though Dick Sobsey might well take that up in the next few posts—but by concentrating on something in Singer’s talk focused on the issue of parental rights and disability. Here is Singer, toward the end of his talk, presenting the perspectives of parents. Singer points out that, as a group, parents of children with disabilities divide over their views of their own children. Although it is a little unclear, even from the fuller context, precisely what “this issue” is that parents divide over, it concerns pain, death, and quality of life:
[This clip is from Singer's talk at the Cognitive Disability conference, podcast #15: 33.30 – 38.02] If you are having trouble playing the video above, the full transcript is provided at the end of the post, and you can also try Youtube directly by clicking right here.
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