Testing Fate: Tay-Sachs Disease and the Right to Be Responsible

Author:   Shelley Z. Reuter
Publisher:   University of Minnesota Press
ISBN:  

9780816699964


Pages:   288
Publication Date:   17 August 2016
Format:   Paperback
Availability:   Temporarily unavailable   Availability explained
The supplier advises that this item is temporarily unavailable. It will be ordered for you and placed on backorder. Once it does come back in stock, we will ship it out to you.

Our Price $39.99 Quantity:  
Add to Cart

Share |

Testing Fate: Tay-Sachs Disease and the Right to Be Responsible


Add your own review!

Overview

In today s world, responsible biocitizenship has become a new way of belonging in society. Individuals are expected to make responsible medical choices, including the decision to be screened for genetic disease. Paradoxically, we have even come to see ourselves as having the ""right"" to be responsible vis-a-vis the proactive mitigation of genetic risk. At the same time, the concept of genetic disease has become a new and powerful way of defining the boundaries between human groups. Tay-Sachs, an autosomal recessive disorder, is a case in point with origins in the period of Eastern European Jewish immigration to the United States and United Kingdom that spanned the late nineteenth and early twentieth centuries, it has a long and fraught history as a marker of Jewish racial difference.In ""Testing Fate,"" Shelley Z. Reuter asks: Can the biocitizen, especially one historically defined as a racialized and pathologized Other, be said to be exercising authentic, free choice in deciding whether to undertake genetic screening? Drawing on a range of historical and contemporary examples doctors medical reports of Tay-Sachs since the first case was documented in 1881, the medical field s construction of Tay-Sachs as a disease of Jewish immigrants, YouTube videos of children with Tay-Sachs that frame the disease as tragic disability avoidable through a simple genetic test, and medical malpractice suits since the test for the disease became available Reuter shows that true agency in genetic decision-making can be exercised only from a place of cultural inclusion. Choice in this context is in fact a kind of ""un""freedom a moral duty to act that is not really agency at all. ""

Full Product Details

Author:   Shelley Z. Reuter
Publisher:   University of Minnesota Press
Imprint:   University of Minnesota Press
Dimensions:   Width: 14.00cm , Height: 3.80cm , Length: 21.60cm
Weight:   0.272kg
ISBN:  

9780816699964


ISBN 10:   0816699968
Pages:   288
Publication Date:   17 August 2016
Audience:   General/trade ,  Professional and scholarly ,  General ,  Professional & Vocational
Format:   Paperback
Publisher's Status:   Active
Availability:   Temporarily unavailable   Availability explained
The supplier advises that this item is temporarily unavailable. It will be ordered for you and placed on backorder. Once it does come back in stock, we will ship it out to you.

Table of Contents

Contents Introduction: A Critical Historical Sociology of Disease Part I. Pathologizing the Other 1. Diagnosing the Genuine “Jewish Type”: Medical Racialism and Anti-Immigration Legislation in the United States 2. Governing Disease: Cultivating the Will to Health in Jewish Immigrants to the United Kingdom Part II. Imag(in)ing Difference 3. “Plainer Than Words Can Describe”: Medical Portraiture and the Visualization of a Jewish Disease 4. The Unethics of Looking at Disease–Disability: Online Representations of Tay-Sachs Part III. Paradoxical Biocitizenship 5. The Right to Be Responsible: Agency and Contemporary Carrier Screening Conclusion: Freedom, Exclusion, and Genetic Decision Making Acknowledgments Notes Bibliography Index

Reviews

Testing Fate illustrates how diseases become racialized, how racializing them supports political projects, and how the medical profession has been instrumental in racial formation. Dorothy Roberts, author of Fatal Invention: How Science, Politics, and Big Business Re-create Race in the Twenty-first Century Shelley Z. Reuter offers a thoughtful, thorough, and sophisticated analysis of themes of modern biocitizenship and belonging refracted through a historical case study of Tay-Sachs disease. Jonathan Kahn, Hamline University As she tells the fascinating and important story of Tay-Sachs disease, Shelley Reuter skillfully reminds us of the tight links connecting our concepts of disease to visions of belonging and otherness, selfhood and social responsibility. Steven Epstein, author of Inclusion: The Politics of Difference in Medical Research


Author Information

Shelley Z. Reuter is associate professor of sociology at Concordia University. She is the author of Narrating Social Order: Agoraphobia and the Politics of Classification.

Tab Content 6

Author Website:  

Customer Reviews

Recent Reviews

No review item found!

Add your own review!

Countries Available

All regions
Latest Reading Guide

MRG2025CC

 

Shopping Cart
Your cart is empty
Shopping cart
Mailing List