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Stillbirth experiences are a traditionally under-researched area of health, with the limited research available focusing on women’s perspectives. Drawing on qualitative interviews with 12 men in Australia who have experienced stillbirth, this article explores how they engaged with their unborn and stillborn child as fathers and the perceived legitimacy of male grief. The results reveal the complex ways in which these men identify as fathers to their unborn and stillborn child; how they develop dynamic and ongoing relationships with their child post-stillbirth; and the problematic of expressing grief in the context of ‘the male role’. Our findings suggest cultural constructions of the ‘male role’ are both manifest and contested in the context of stillbirth, and that fathering and grief are situated within a highly gendered and relational dynamic. These findings suggest that further work is needed to explore and conceptualize the interplay of gender identity and bereavement for Australian men. [ABSTRACT FROM PUBLISHER]

Drawing on in-depth interviews with Australian cancer patients, this article examines their experiences of utilizing complementary and alternative medicine (CAM) within disease and treatment processes. Results illustrate the complex and often contradictory roles played by CAM within patients' therapeutic trajectories. On the one hand, their accounts illustrate the liberating and positive impacts of CAM engagement, including perceived increases in feelings of control, power and individual autonomy within therapeutic processes. However, the interviews also revealed problematic notions of self-healing and hyper-positivity engendered in much CAM practice, involving the imposition of restrictive notions of self-discipline on these cancer patients. On the basis of the results it is argued that CAM sociology must refocus on the grassroots experiences of different patient groups, rather than grandiose notions of wider socio-cultural shifts in therapeutic practice. [ABSTRACT FROM AUTHOR]

Being diagnosed with a life-limiting illness entails a fundamental reshaping of one's relationship with the future. From ‘bucket lists’ of destinations and experiences to ‘flights of hope’ for experimental or specialised medical care, diagnoses of serious illness are deeply entwined with travel in Australian cultural narratives. In this paper, we draw on a thematic analysis of interviews with cancer patients and their carers to ask what meanings are attached to narratives of travel – whether completed or constrained, imagined or interrupted – in the context of a cancer diagnosis. Focusing on narratives of travel draws attention to themes of disruption, resilience, autonomy and living a meaningful life within the precarious timescape of cancer. Through this analysis of time and travel, we examine how normative expectations of how to live with or beyond cancer can produce tensions, particularly in the uncertain but precariously hopeful landscape of precision cancer treatments. [ABSTRACT FROM AUTHOR]