Abstract:While humanitarian communication has been scrutinized by practitioners and academics, the role and meanings of intimacy at a distance in this communication have been largely overlooked. Based on analysis of 17 in-depth interviews with professionals in 10 UK-based international NGOs engaged in planning, designing and producing humanitarian communications, this article explores how intimacy figures in NGOs' thinking about and practice of humanitarian communication. Drawing on discussions of 'intimacy at a distance' and the 'intimization' of the mediated public sphere, the analysis explores three metaphors of intimacy used by interviewees to articulate the relationships they seek to develop with and between their beneficiaries and UK audiences: (1) sitting together underneath a tree; (2) being there; and (3) going on a journey. The paper situates the governance of intimacy of practitioners' thinking and practice as NGOs' attempts to respond to criticisms from the humanitarian and international development sector, policymakers and scholars. It concludes by calling for a revisiting of the 'tyranny of intimacy' in humanitarian communication, outlining its implications for both academic scholarship and practice.
This paper explores women's experiences of shame as a political, existential and psychological emotional state. In particular, it focuses on women's accounts of the specific shameful experiences containing the employment of a 'façade' to protect the 'true' self constructed as inadequate and shameful. The key argument in this paper is that women's shame should be understood as discursively, politically and psychodynamically over-determined. It therefore presents a reading of women's shame that brings together Foucauldian ideas of self-surveillance and positioning in discourse, with a psychodynamic theorization of shame as resulting from a constant negotiation between external forces and internal agencies. The paper also argues for the necessity of a multiplicity of readings to make adequate sense of such over-determination.
This article provides a critical review of recent psychological articles on prosocial behaviour. Even though it focuses on a specific section of this literature – giving to charities and prosocial responses to humanitarian disasters – the paper aims to offer a wider critique as it interrogates the epistemological and methodological underpinnings of the prosocial literature as a whole. It aims to illustrate how the problematic aspects of traditional quantitative, deductive, experimental research in prosocial behaviour in general, when applied to giving to charities, preclude a deeper and more complex understanding of a phenomenon quintessentially social and altruistic. I identify three specific issues that make mainstream approaches to prosocial behaviour problematic and limited in scope. The first relates to the insularity of mainstream psychology and the lack of contextualisation of its findings, in particular the problematic neglect of ideological and socio‐historical factors in prosocial behaviour. The second relates to mainstream psychology's disregard for the role played by conflict, contradiction and ambivalence, in attitudes and decision making as well as in the emotional aspects of prosocial behaviour. The third looks at the constraints imposed by scientifically inspired methods, how they predetermine the range of participants' responses and make it hard to apply the findings to real life situations. I claim that these epistemological and methodological constraints severely limit the applicability and comprehensiveness of current research. The discussion of these issues is woven through the review and uses some specific studies to illustrate the limitations imposed by these constraints. Throughout the paper I also argue for the need to incorporate a psychosocial approach to research into prosocial behaviour.
This paper draws on a study that asked twenty family users about their first session of family therapy. Analyses of the interviews indicated that families entered therapy with a pre-existent knowledge about therapy, which did not always chime with those of professionals and which positioned speakers in ways which governed their expectations and perceptions of therapy. This paper, therefore, is concerned with the acquisition and deployment of knowledge: specifically, the knowledge involved in being a user of family therapy. Three key discourses were identified through this analysis: medical, counselling and consumerist. We aim to illustrate how these discourses served as a resource for members of the family in constructing therapists, therapy and themselves in relation to their experience. The examination of the rhetorical, ideological and practical effects of the positions chosen and the objects constructed, in terms of how speakers wanted to present themselves, with what enhanced or diminished status as patients, shows users actively engaging with the power of therapeutic institutions. Users' accounts suggest that while most speakers felt anxious about the prospect of therapy, there were clear differences in overall satisfaction/dissatisfaction with the experience according to the synchrony between speakers' construction of the therapist, and themselves as client/ patients. Those who seemed to take a traditional view of therapy within a medical discourse valued therapists who offered diagnosis and a cure; those who sought and experienced a counselling relationship with the therapist found their experience to be constructive in terms of enhanced selfknowledge. We believe that the research findings discussed in this paper have implications for family therapists in accommodating to parental and child positions to maximise the effectiveness of therapy and so minimise drop-out.
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