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Shelley Z. Reuter, Testing Fate: Tay-Sachs Disease and the Right to be Responsible (Minneapolis, MN: University of Minnesota Press, 2016), pp. 264, $27,00, paperback, ISBN: 978-0-8166-9996-4.

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Shelley Z. Reuter, Testing Fate: Tay-Sachs Disease and the Right to be Responsible (Minneapolis, MN: University of Minnesota Press, 2016), pp. 264, $27,00, paperback, ISBN: 978-0-8166-9996-4.

Published online by Cambridge University Press:  06 March 2017

Lundy Braun*
Affiliation:
Brown University, USA
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Abstract

Type
Book Review
Copyright
© The Author 2017. Published by Cambridge University Press. 

What is the political and epistemological significance of racialisation in medicine? What are the social processes by which racialisation occurs? Shelley Z. Reuter’s thought-provoking Testing Fate makes a much-needed contribution to the scholarly literature on the interconnections between racialisation, disease construction, knowledge production and political economy. While much has been written about race and sickle cell disease, there has been remarkably little critical scholarship probing the history of Tay-Sachs and its racialisation. Building on Michael Omi and Howard Winant’s concept of racial formation, Reuter argues that making Tay-Sachs an exclusively Jewish disease can best be understood as a ‘racial project’. This engaging book thus fills an important lacuna in the literature on racial formation in medicine.

First known as amaurotic familial idiocy in Jewish immigrants by physicians in both the UK and US in the late 1800s, Tay-Sachs is a rare and devastating neurological disease with no treatment. In 1970, there were only about 50–60 cases per year in the US and Canada, 40–45 of which occurred in people of Ashkenazi Jewish descent. Most accounts of this autosomal recessive disease have ignored non-Jewish Tay-Sachs. Since mass screening for Tay-Sachs began in the 1970s, the disease has been largely eliminated in Jews. Consequently, most cases now occur in non-Jewish groups. Yet, despite evidence to the contrary, Tay-Sachs disease, together with sickle cell disease, remain prototypical race-specific diseases in the scientific and popular imagination.

Testing Fate is a nuanced transnational analysis of the historical processes by which Tay-Sachs Disease became a marker of racial difference in Jews. Reuter organises the book into three parts – ‘Pathologizing the Other’; ‘Imag(in)ing Difference’; and ‘Paradoxical Citizenship’. In the first two chapters of this theoretically rich and deeply researched book, she draws on sociological theories of disease construction in Michel Foucault and Nicholas Rose, critical race studies and close readings of scientific texts to demonstrate the almost immediate attachment of Tay-Sachs disease to Jewish bodies in the late 1800s. Although there was large-scale immigration of eastern Europeans, many of them Jewish, to both the UK and the US in the late nineteenth century, Reuter provides fascinating evidence that the processes of racialisation, while intersecting and cross-fertilising at certain historical moments, differed in the United Kingdom (UK) and the United States (US) – and had different outcomes. In the US, the identification of Tay-Sachs in eastern European Jews drew on and contributed to cultural anxieties about disease race and degeneration in a period of rising nativism and unemployment. Stereotyping descriptions of Tay-Sachs were part of scientifically informed policies that materialised in angry immigration debates and ultimately the Immigration Act of 1924 that severely restricted immigration from certain regions of the world. In the UK, on the other hand, Jewish immigration mobilised concerns about integration, rather than exclusion, with established Jewish organisations, such as the Jewish Board of Guardians actively intervening to assimilate the eastern European other. Interestingly, it is in these discourses of assimilation in the UK that Reuter locates the origins of ‘the right to be responsible’ (p. 19) or medical ‘responsibilisation’, as represented in twentieth-century genetic counselling and screening programs embraced by Ashkenazi Jews in the US. For a variety of reasons, mass screening never took off in the UK.

In the second section of her book, Reuter examines the rhetorical power of visual imagery in scientific descriptions and online portrayals, such as YouTube videos, of Tay-Sachs patients. Reductive scientific imagery deployed by Jewish and non-Jewish scientists was intertwined with and central to anti-immigrant discourses. With privileged access to the ‘truth’, scientific visual imagery of cells, tissues, disabled children and the signature cherry-red spot in the macula of affected babies contributed to the construction of categories of Jews as fixed types. In ‘making a spectacle of these children’ (p. 124), online portrayals of Tay-Sachs served multiple functions, including education, cultivation of a sense of belonging and construction of categories of personhood, as well as a ‘morbid voyeurism’. Both types of visual representations shaped and were shaped by racialised narratives.

In the last section of the book, Reuter situates responsibilisation in the political and cultural context of neo-liberalism. Linking historical scientific discourses to contemporary practices of biocitizenship, Testing Fate raises important questions of ‘constrained agency’ in the context of the complex and changing relationships of Jewish communities to racialisation. With the identification of Hexoaminadase A deficiency in Tay-Sachs patients in 1969, mass screening for enzyme activity became a possibility, a ‘right’, and a societal imperative. Because there was no treatment for Tay-Sachs, containing the disease turned on prevention, either management of marriage between carriers or more commonly prenatal screening followed by abortion. Racialisation of Tay-Sachs thus served exclusionary public policies but it also served to shape notions of belonging for the excluded other.

This well-written and nuanced analysis of Tay-Sachs as a Jewish disease contains many additional insights relevant to current debates over racialisation projects that have intensified in medicine since the first draft of the human genome was announced in 2000. Attentive to the changing meanings of Tay-Sachs over time, Reuter demonstrates that racialisation operates on multiple terrains; it is about silences as much as what is visible. Enacted in a variety of ways, attaching racial meaning to Tay-Sachs also required ignoring or actively dismissing Tay-Sachs in non-Jews. Yet, for all the historical shifts ‘what has remained constant throughout the history of this disease category is its deployment as a way to delineate, exclude, and regulate the other’ (p. 118).

While some scholars have argued that scientific racism was rejected after the Second World War, Reuter’s analysis of Tay-Sachs argues that there was no such retreat from scientific racism in the medical sphere. Testing Fate thus adds crucial insights to recent scholarly inquiries into how stigmatising narratives about race and racial difference persist in the ever-expanding era of genetic testing. This well-written and fascinating account of the history of a racialised disease should be read by both health care providers and scholars in a wide range of fields interested in the history of race and medicine.