Can Cultural Values Help Explain the Positive Aspects of Caregiving Among Chinese American Caregivers?

This study used an adaptation of the caregivers' stress model to examine the positive aspects of caregiving with 113 Chinese American family caregivers who provided care to their elderly relatives. The hierarchical multiple regression analysis indicated that combination of caregiver background characteristics, stressors, and cultural values had direct effects on positive aspects of caregiving. Unlike previous studies in which cultural values were not measured, this study found that cultural values helped explain positive aspects of caregiving. Specifically, cultural values, caregiver's health, and caregiver's age predicted positive aspects of caregiving. Service implications are discussed based upon the findings.     

The challenges of a hidden disability: Social work practice in the field of traumatic brain injury

Abstract

Traumatic brain injury (TBI) has become an important area for social work practice. Children and adults sustaining TBI often undergo hospitalisation, rehabilitation and face the prospect of lifelong cognitive and psychosocial impairments. Families are profoundly affected by the consequences of the injury. TBI is a ‘hidden disability’ because there are typically no physical markers indicating a person has brain damage. This paper aims to provide some guidelines for social work practice in the area, in particular, outlining options for social work interventions at individual, family, community, service system and policy levels. Social workers need to acquire specialised knowledge about brain injury, reformulate traditional models of grief counselling to address the adjustment challenges and utilise community education and service innovation to address the social stigma and reduced level of community participation associated with brain damage. Finally, social workers aim to nurture a sense of hope in the face of the tragedy.     

Walking,sensing, belonging: ethno-mimesis as performative praxis

This article outlines a research project that used participatory action research (PAR) and arts practice (ethno-mimesis) to explore the senses of belonging negotiated by asylum seekers, refugees and undocumented migrants in the English East Midlands. At the core of this project was a walking event in which refugees and new arrivals guided long-term residents through the city, tracing an imaginary and real journey that linked the here and now with the then and there. Reflecting on the ways that walking evokes and invokes, this article suggests that while walking should not be privileged as a way of knowing, it has certain sensate, embodied, relational and collective attributes which rendered it particularly useful as a means of exploring the importance of being-in-place among a group whose lives are often depicted as markedly transnational.     

The Securitization of Migration: A Racial Discourse1

As we enter the informational economy, freedom of human mobility has nearly disappeared. Instead, powerful words are travelling the globe unhindered: risk and security. They are being strung together with the present “migration phenomena”, leaving migrants bound by the chain of the new security discourse: the securitization of migration. This discourse is racism's most modern form. Discursive practices, as seen through the press portrayal of 599 migrants reaching Canada's western coast, have transformed migrants into agents which threaten “human security” How discourse informs government policy is illustrated through an examination of Canada's new immigration legislation.     

Accounting for Disability: Customer feedback or citizen complaints?

This paper has two aims. First, it will summarise the findings of a study of the views and experiences of adults with acquired physical impairments. This entailed taking open-ended accounts from respondents in order to elicit their concerns and experiences. The paper will focus on two aspects of data from the study: views about health and social services; and those about citizenship. The second aim of the paper is to situate the role and status of personal accounts of disability within the health and social policy context of recent years, which has been characterised by both consumerism and an intensification in the activities of the disability movement. In the run up to the 1990 NHS and Community Care Act, it became clear that the purchasers (now 'commissioners') of health and social services would be encouraged to elicit users' views of services, to engender a needs-led not provider-led approach. Later in the paper we will discuss the relationship between this officially endorsed consumerism and the concerns of disabled people when voicing their views. It will be argued that personal accounts of disability have gained a cultural currency because of the convergence of processes linked to consumerism within recent British health and social policy on one side and new social movements on the other.