Table Of Content

eae Volume 2003 Editors Robert Dingwall. Veronica James, Elizabeth Editorial Assistant Allison Pearson Review Editors Susan Gregory and Carol I| Vionograph Edit Jonathan Gabe Chy airperson J1 udi1 th1 GreenA \ Davina Allen Marina Barnard Yoav Ben Shlomo Elizabeth Ettorre Rob Flynn Linda McKie James Nazroo Clive Seale Jonathan Tritter Andrew Webster Clare Williams Blackwell Publishing Oxford, UK and Boston, USA Contents ‘About a year before the breakdown I was having symptoms’: sadness, pathology and the Australian newspaper media (Rowe, Tilbury, Rapley and O'Ferrall) 680 A subtle governance: ‘soft’ medical leadership in English primary care (Sheaff, Rogers, Pickard, Marshall, Campbell, Sibbald, Halliwell and Roland) 408 Belief, knowledge and expertise: the emergence of the lay expert in medical sociology (Prior) S41* Beyond ‘Beer, fags. egg and chips’? ) Exploring lay understandings of social inequalities in health (Popay, Bennett, Thomas, Williams, Gatrell and Bostock) | Bio-phobias/Techno-philias: virtual reality exposure as treatment for phobias of ‘nature’ (Davidson and Smith) 644 Blurring, moving and broken boundaries: men’s encounters with the pregnant body (Draper) 743 Changes in mental health status amongst children of migrants to Australia a longitudinal study (Alati, Nayman, Shuttlewood, Williams, and Bor) 866 Corps de Ballet: the case of the injured ballet dancer (Turner and Wainwright) 269 Cystic fibrosis, classification and genetics (Hedgecoe) 50 Depressive symptoms in The Netherlands 1975-1996: a_ theoretic: framework and an empirical analysis of socio-democratic characteristics, gender differences and changes over time (Meertens, Scheepers and Tax) 208 Divided care and the Third Way: user involvement in statutory and voluntary sector cancer services (Tritter, Barley, Daykin, Evans, McNeill. Rimmer, Sanidas and Turton) 429 -mpty ethics: the problem with informed consent (Corrigan) 168 “nforcing patient rights or improving care? The interference of two modes of doing good in mental health care (Pols) — 320 “nvisaging the embryo in stem cell research: rhetorical strategies and media reporting of the ethical debates (Williams, Kitzinger and Henderson) 793 ‘amily stories and the use of heuristics: women from suspected hereditary breast and ovarian cancer (HBOC) families (Kenen, Ardern-Jones and Eeles) $38 Gender, Violence and Health Care: Implications for Research, Policy and Practice (McKie) 120 Going public: references to the news media in NHS contract negotiations (Hughes and Griffiths) 571 Health and Media: An Overview (Seale) 513 | Publishing Ltd/Editorial Board 2003 Healthy viewing: the reception of medical narratives (Davin) ‘Ignorance is bliss sometimes’: constraints o1 ‘informed patient’ in the changing landscapes of (Henwood, Wyatt, Hart and Smith) 589 Lay experiences of health and illness: past research (Lawton) 25° Life on a slippery slope: perceptions of health in adults \ (Lowton and Gabe) 289 Making connections: studies | le social organisation (Griffiths) S$ Making health services management research critical: a suggestion (Learmonth) 93 Media activism and Internet use by people with HIV/AIDS (Gillett) 608 Medicine as discursive resource: legitimation in the W' OrK-| N‘ arratiavee s Ol f midwives (Foley and Faircloth) 165 Menopause as a long-term risk to health: implications of general practitioner accounts of prevention for women’s choice and decision-making (Murtagh and Hepworth) 185 Narrativity and the mediation of health reform agendas (Hodgetts and Chamberlain) 553 Popular media and ‘excessive daytime sleepiness’: a study of authority in medical sociology (Kroll-Smith) 625 Pregnancy, illness and the concept of career (Thomas) 383 ‘Radical blueprint for social change’? Media representations of Labour's policies on public health (Davidson, Hunt and Kitzinger) Reporting the dawn of the post-genomic era: who wat live fore (Smart) 24 Representing childhood cancer: accounts from newspapers and parents (Dixon-Woods, Seale, Young, Findlay and Heney) 143 Signifying across time and space: a case study of biomedical educationa texts (Carter and Michael) +> 44 Some of our concepts are missing: re ‘f} lect+; ion. s on + thhea e absence“ 2 of f a soci“Aoll ogyr \ of organisation in Sociology of Health and Illness (Davies) S] Support for non-conventional medicine in Israel:] cognitive coherence (Leiser) 457 Technology and medical practice (Heath, si" The body and doing gender: the relations between doc hospital work (Davies) 720 The determinants of health: structure, context and agency (Williams) S131* The downside of Viagra: women’s experiences and concerns (Potts, Grace, Vares and Favey) 679 The illness experience: state of knowledge and perspectives for research (Pierret) S4* Blackwell Publishing 910 Contents The impact of papers in Sociology of Health and Illness: a bibliographic study (Armstrong) S58* The meaning of complementary and alternative medicine practices among people with HIV in the United States: strategies for managing everyday life (Foote-Ardah) 481 The practice of medical technology (Timmermans and Berg) $97 The use of quantitative medical sociology (Blane) S115* Towards a new perspective on deliberate self-harm in an area of multiple deprivation (Redley) 348 [ransforming general practice: the redistribution of medical work in primary care (Charles-Jones, Latimer and May) 71 Understanding women’s sleep management: beyond medicalization- healthicization? (Hislop and Arber) — 815 *Page numbers beginning with ‘S’ refer to the Silver Anniversary Issue (25:3) Blackwell Publishing Ltd/Editorial Board 2003