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Disability and the Welfare State in Britain

Changes in Perception and Policy, 1948-1979

 

Jameel Hampton

 

Bristol: Policy Press, 2016

Hardcover. ix+277 p. ISBN 978-1447316428. £70

 

Reviewed by Robert McRuer

George Washington University (Washington, DC)

 

 

 

In order to appreciate one of the main strengths of Jameel Hampton’s Disability and the Welfare State in Britain: Changes in Perception and Policy, 1948-79, it is useful to appreciate, first, the extremely dire situation in which disabled people in Britain found themselves before, during, and after the year of the book’s publication in 2016. The global pandemic of COVID-19 meant that 2020 was extremely difficult; in fact, even though disabled people composed an estimated 16% of the population, they accounted for 59% of the deaths from the disease. As 2020 began, however, disabled people were already concluding one of the most difficult decades in a century. Since 2010, they had been subject to one of the most punishing austerity regimes in the world, initially put in place by a coalition government headed by the Tory leader David Cameron and the Liberal Democratic Leader Nick Clegg. In response to the global economic crisis of 2008 and the supposed “emergency” of over-spending and budget deficits, the coalition government instituted massive cuts to social services. Disabled people’s already-meager statutory benefits were shrunk, streamlined to a universal payment, or eliminated altogether. They were subject to short and often-degrading assessment tests, carried out by private contractors, measuring their “fitness” for work (a fitness that would often make them ineligible for benefits). Sanctions were imposed (and more benefits cut) if an assessment was missed or if recipients could not provide evidence of a search for employment. A notorious policy that came to be called the “bedroom tax” reduced benefits if homes were deemed to have “excess” living space (usually one spare room). Throughout the decade in which Hampton’s book appeared, the popular press, and by extension the general public, increasingly stigmatized disabled people as “scroungers” or “malingerers.” The coalition’s austerity regime impacted innumerable nondisabled people as well, but in almost all areas of public life, disabled people in the UK arguably felt the brunt of austerity cuts. Radical activist groups such as Disabled People Against Cuts (DPAC) formed to counter what was seen as a concerted attack on the rights and dignity of disabled people. To many, what was happening during the decade was the culmination of almost four decades of neoliberal capitalism, associated most famously with Margaret Thatcher’s attack on worker’s rights, human rights, big government, the welfare state, and indeed any notion of a collective “society,” which she famously declared did not exist. Innumerable commentators have looked to Thatcherism and the beginning of neoliberalism for the roots of the challenges disabled people face in the twenty-first century.(1)

And yet, Disability and the Welfare State in Britain arguably provides a sharp check on a presentism that would position disability oppression as primarily augmented by the Thatcherist dismantling of the welfare state from 1979 forward. Although this is not actually its stated purpose, the book’s main strength is its comprehensive overview of the ways in which disability oppression was already rooted in the period that preceded the rise of neoliberal capitalism, a period that is often romanticized by critics of Thatcherism for its social solidarity and strong government safety net. Disabled people, Hampton makes clear, were effectively excluded from the welfare state from its inception for various reasons. And when they finally emerged into the consciousness of politicians and the media in the 1960s and 1970s, largely because of concerted activism that Hampton details, the gains that could be acknowledged in the 1970s were small and short-lived. Thatcherism and neoliberal capitalism are thus only the latest chapter in a longer story of disability oppression, neglect, and exclusion. Disability and the Welfare State in Britain is thus history at its best in that it implicitly challenges unchecked assumptions held in the present and encourages readers to locate disability exclusion and resistance in a longer and much more multi-faceted story.

Hampton first quickly traces the history of provisions for disability by the state and by non-state entities back several centuries as he sets up his thick central chapters focused on the years 1948-79. The two key dates prior to the twentieth century are 1601, when the Old Poor Law Act was established, giving local parishes responsibility for assisting those in need, and 1834, when the Poor Law Amendment Act was established, focused more on the institutionalization of disabled people and on efforts to determine that their need was “genuine.” This nineteenth-century moment helped to codify a cultural distinction between “deserving” and “non-deserving” poor that persists in various ways into the twentieth and twenty-first century. Also culturally codified from the nineteenth century forward was a suspicion that certain people might be taking advantage of the system.

Hampton then shows how the period leading up to the establishment of the welfare state inaugurated a will to eliminate some of the great evils of society, including poverty and want. Although there are many ways in which it would seem counter-intuitive that disabled people would not be part of this initiative, Hampton surveys several reasons why they were essentially excluded from the post-World War II settlement; that is, during the period stretching from 1948-67. First, a cultural belief in a “contributory principle” existed that connected insurance and statutory benefits to a citizen’s (or, really, worker’s) contribution to the greater whole. This was correlated with the fact that, regardless of how groundbreaking or generous the welfare state might be understood to have been, it was nonetheless part of a work-based system, a system that by definition excluded many disabled people. Second, especially early on in the establishment of the welfare state, there was a lingering sense that disabled people should be provided for in non-statutory, charitable, ways (arguably a holdover from the Poor Laws of previous centuries). Third, and connected to the contributory principle, a division between “deserving” and “non-deserving” was evident during the initial post-war period in the fact that certain groups did receive attention and some statutory assistance; namely, disabled veterans and those who had been injured on the job. Finally, the initial welfare state had a strong universalist bent that discouraged (and arguably stigmatized) particular groups, such as disabled people, in need of aid or benefits.

As in many other periods (and sites) of disability history, activism begins to change this during the late 1960s and heading into the 1970s. Another strength of Hampton’s book is thus its solid and groundbreaking overview of the group Disablement Income Group (DIG), founded in 1965 by Megan du Boisson. No other thorough history of DIG exists. Hampton rightfully credits DIG with bringing disability to the consciousness of politicians and the public in the 1960s; as their name suggests, their goal was to secure policy changes that would guarantee an income for disabled people in particular and regardless of any past contribution to the state or economy. Initially, DIG focused on a group self-identifying as “disabled housewives,” but the scope of their work expanded over time. DIG can be credited with significant successes. Their advocacy surely nurtured the Chronically Sick and Disabled Persons Act (CSDP) of 1970, and as the decade began, they had secured something of a cross-party consensus that a guaranteed statutory income was indeed important for disabled people. Even during the economic crises of the 1970s, DIG managed to secure allies in both the Conservative and Labour parties. Still, the CSDP largely failed to provide tangible benefits, and Hampton argues that the view of disabled people as scroungers solidified in its wake. Most importantly, on a more intangible cultural level, the CSDP “did not create lasting respect, dignity and acceptance” [216]. The DIG’s narrow focus on a universal income also at times limited the risks the group was willing to take. More radical groups like the Union of the Physically Impaired against Segregation (UPIAS), a group Hampton largely locates in footnotes, had a more expansive vision of cultural change and integration. Indeed, more on UPIAS would have been welcome, as UPIAS’s argument for what came to be called the social model of disability marks the group as a precursor to late twentieth and early twenty-first century critical disability studies. The transformed consciousness put forward by UPIAS is arguably a condition of possibility for studies like Disability and the Welfare State in Britain.

It is ironic, perhaps, that the word capitalism appears very rarely in Hampton’s study, as—again—one of the main strengths of the books is that it allows perceptive readers to see various moments within the history of capitalism, not just neoliberalism, as oppressive for disabled people. If on a macroeconomic level, the mid-twentieth century is associated with mass production and consumption, on a microlevel, the level of everyday life, it was an era of uniformity and normalization (codified, as Hampton implicitly demonstrates, in the universalist thinking of the welfare state). Normalization and uniformity, as disability studies has long shown, are invariably oppressive to disabled people.(2)

It is important to keep in mind (and Hampton’s book makes this quite clear even if it does not state it explicitly) that the welfare state was a reformist compromise within capitalism, not a revolutionary transformation. Indeed, the words of Franklin Delano Roosevelt make that crystal clear, on the other side of the Atlantic (ironically, given Roosevelt’s own disability). In a meeting with capitalist leaders to justify the much weaker welfare state-light reforms in the United States, Roosevelt asserted,

I was convinced we’d have a revolution in [the] US and I decided to be a leader and prevent it. I’m a rich man too and have run with your kind of people. I decided half a loaf was better than none—a half loaf for me and a half loaf for you and no revolution.(3)

Cynicism like Roosevelt’s is not immediately obvious in Hampton’s study of Britain, but the larger point remains that the welfare state in both locations was a compromise within the history of capitalism. Neoliberal capitalism has been so bad for disabled people that it is possible to forget that capitalism in general has been, consistently, oppressive. Hampton’s detailed study, even if inadvertently, makes that point clearly.

Another minor strength of Hampton’s book could be seen as a cultural studies strength. The book is not simply a dry history of policy changes (although it is often that); it also at times makes clear that struggles occur within language and representation. The clearest example of this is in Hampton’s overview of the moment when children whose mothers had been prescribed thalidomide mid-century burst onto public consciousness in the late 1960s and early 1970s. This occurred within the media and generated a widespread sense that something needed to be done to provide for these children. DIG, interestingly, did not take advantage of this moment of public outrage, because they were wary of pushing Conservative and Labour allies too far and too quickly. But Hampton’s overview demonstrates that change happens in complex and at times contradictory ways. Hampton does not fully draw out the contradictions; indeed, he himself repeats without commentary the language of “tragedy” and “victim” [163, 165] that later disability activists would repudiate (including UK artists and activists impacted by thalidomide, such as Mary Duffy or Mat Fraser). Hampton’s overview of the moment, however, provides a provocative example of how and why representation, even compromised representation, matters and how it works.

There are other moments when Hampton’s language can be criticized; contemporary disability acvitists and scholars would never describe a wheelchair user, for instance, as “wheelchair-bound” [155]. Nonetheless, Disability and The Welfare State in Britain is a vitally important history that arguably allows for the most textured understanding of how disabled people were understood in shifting ways during the consolidation of the British welfare state. Reading backwards from 2020, when the challenges of COVID-19 and a decade of austerity might lead readers to forget or minimize the extreme challenges of earlier eras, Hampton’s study is indispensable.

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(1) For more on these challenges, see Robert McRuer, Crip Times : Disability, Globalization, and Resistance. New York: NYU Press, 2018.

(2) The work of Kevin Floyd is particularly useful for thinking about the relationship between macroeconomic processes and quotidian, microlevel practices. Kevin Floyd, The Reification of Desire : Toward a Queer Marxism. Minneapolis: University of Minnesota Press, 2009.

(3) Quoted in Neil Smith, The Endgame of Globalization. New York: Routledge, 2005 : 86.

  

                     


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