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98 Benefits Number 43 • Volume 13 • Issue 2 Disability: rights, work and security Marilyn Howard Disability is a complex and contested issue, often with tensions between policy approaches of ‘benefits’ and ‘rights’, that is, benefits as compensation for exclusion rather than civil rights to enable inclusion (Daniel, 1998). These intersect with different models of disability (medical, social and transactional: Howard, 2003). Traditionally, the medical model has been the ‘moral basis’ for benefits (SSAC, 1997), although increasingly the social model is accepted
163 Why have disability categories in social security? Deborah Mabbett The specification of categories (for example, unemployment, old age, disability) is a well-established feature of social security. However, disability categories are problematic: the evidence on which decisions have to be made is complex, and understandings of the nature of disability are highly contested. Disability categories could be reformed by unification with other categories used in the same policy area (for example, unemployment) or by fragmentation into new, smaller categories
Key messages Public survey evidence produces official portraits of disability and also hidden figures of disabled people. No one model of disability offers a complete depiction of the diverse lived realities for disabled people. Each model casts some light and shadows on the multiplicity of experiences of disabled people. During the COVID-19 global pandemic we can observe a damning revelation of the dire conditions of the uncounted disabled and poorly supported disabled, particularly the homeless and seniors in long-term care facilities and nursing
175 Disability Working Allowance: what was the point? Norman Cockett Disability Working Allowance (DWA) was introduced in 1992 as a benefit to top up the wages of disabled people working 16 hours a week or more. This was the first major attempt, within UK social security policy, to help disabled people take up and remain in paid jobs. The formal evaluation of DWA suggested that the benefit had failed in a number of respects. The purpose of this article is to reflect on what was achieved by introducing DWA. The author looks at the stated objectives and other
disabilities, in the state of Mato Grosso do Sul (MS). We briefly draw on conceptualisations of Indigenous persons, disability and children, and review national and international legislation that deals with the rights of children, Indigenous people and people with disabilities, to identify how the legislation addresses the issue. This also serves to present the normative framework for these topics as currently in force in Brazil. We then introduce the Kaiowá and Guarani people, inhabitants of the region of Dourados in the state of MS, in central-western Brazil, offering a
Introduction In this article we look at systemic violence: the ‘life-shattering violence caused by decisions that are made in parliamentary chambers and government offices’ ( Cooper and Whyte, 2017 : 1) with regard to people with severe disabilities who are in receipt of disability benefits in the UK. We explore how this systemic violence is intrinsic to the political and social practices of maintaining a neoliberal welfare regime, with its predisposition towards the harmful targeting of populations on the wrong side of inequality, unable to meet the demands
Policy & Politics vol 30 no 3 387 © The Policy Press, 2002 • ISSN 0305 5736 English Mental health service users/survivors are subject to both mental health and disability policies, yet there appears to be an ambiguity in the approach of disability policy and disability politics to them. Mental health policy, which has always had powers to restrict their rights, is now increasingly associating mental health service users/survivors with ‘dangerousness’ and focusing on them as a threat to ‘public safety’. Mental health service users’/survivors’ organisations
In recent years the pace of reform in health policy and the NHS has been relentless. But how are policies formed and implemented? This fully updated edition of a bestselling book explores the processes and institutions that make health policy, examining what constitutes health policy, where power lies, and what changes could be made to improve the quality of health policy making. Drawing on original research by the author over many years, and a wide range of secondary sources, the book examines the role of various institutions in the formation and implementation of health policy. Unlike most standard texts, it considers the impact of devolution in the UK and the role of European and international institutions and fills a need for an up-to-date overview of this fast-moving area. It features new case studies to illustrate how policy has evolved and developed in recent years. This new edition has been fully updated to reflect policies under the later years of New Labour and the Coalition government. Although written particularly with the needs of students and tutors in mind, this accessible textbook will also appeal to policy makers and practitioners in the health policy field.
Risk has emerged as a key mechanism for controlling the future and learning from past misfortunes.
How did risk influence policy makers’ responses to COVID-19? How will they be judged for their decisions?
Drawing on case studies from the UK, China, Japan, New Zealand and the US, this original text explores policy responses to COVID-19 through the lens of risk. The book considers how different countries framed the pandemic, categorised their populations and communicated risk. It also evaluates the role of the media, conspiracy theories and hindsight in shaping responses to COVID-19.
As we reflect on the ‘first wave’, this book offers a vital resource for anticipating future responses to crises.
Providing an account of the policy response to COVID-19 in England, this book analyses the political and long-term systemic factors associated with the failures to control the first wave of the pandemic during 2020.
It explores the part played by key policy actors, particularly politicians and scientists, and focuses on two difficult policy issues during the first wave: the establishment of a ‘test, trace and isolate’ system and responses to the high death rate in care homes for older people.
Drawing on a wide range of documentary evidence, including parliamentary papers and SAGE minutes, this book draws attention to the importance of longstanding structural problems in public health and the care sector, especially the impact of outsourcing and privatisation.
