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give or receive care ( Knijn and Kremer, 1997 ). At the heart of this exclusion is the value (or lack thereof) placed upon care and its association with the private domain. Tronto (1993) suggests that the inability to think of care outside of privatised and gendered terms is not a failure of care, but a constraint in the social contexts in which caring practices occur in society. Exclusionary practices particularly affect women with disabilities, whose parental rights are not always recognised. For many mothers with disabilities, especially those with intellectual
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
159 Critical and Radical Social Work • vol 2 • no 2 • 159–74 • © Policy Press 2014 • #CRSW Print ISSN 2049 8608 • Online ISSN 2049 8675 • http://dx.doi.org/10.1332/204986014X13986987417481 article Out of the shadows: disability movements Roddy Slorach,1 UK rslorach13@gmail.com Britain’s disability movement can be divided into two distinct phases. The first, reaching a peak in the late 1980s to mid-1990s, was seen by its leading activists as a civil rights movement, whereas the second has been a response to the recent and ongoing government spending cuts. The
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
Introduction Older adults living with disabilities in Canada often require assistance from a relative or friend (that is, a family carer) ( Kokorelias et al, 2020 ). Based on 2012 estimates, 13.7 per cent of the Canadian population (4.8 million Canadians) lived with disabilities ( Statistics Canada, 2013 ) and 28 per cent of the population (9.7 million Canadians) aged 15 and above provided unpaid care to a family member, friend or neighbour ( Fast, 2015 ). While 74 per cent of carers spent under ten hours per week on care, 10 per cent of them provided unpaid
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
Introduction Support coordination refers to assistance provided to effectively navigate and implement cohesive and collaborative services and supports across various systems and sectors. For people with disability and complex needs, it should optimise service provision coordination and reduce the risk of inadequate and inefficient services. If appropriately designed and performed, support coordination should lead to: better understanding of individual need; informed choices about appropriate providers; stronger relationships and communication with service
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
