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This section offers news briefs from the National Environmental Health Association (NEHA) as of July 2024. A toolkit for Body Art Model Code adoption for jurisdictions has been developed. A Disaster Readiness Simulator is under development to enable organizations to test and understand emergency response capabilities and human resource capacities. The 17th International Federation of Environmental Health World Congress was held in Perth, Western Australia.

Diagnoses of infectious diseases are being transformed as mass self‐testing using rapid antigen tests (RATs) is increasingly integrated into public health. Widely used during the COVID‐19 pandemic, RATs are claimed to have many advantages over 'gold‐standard' polymerase chain reaction tests, especially their ease of use and production of quick results. Yet, while laboratory studies indicate the value of RATs in detecting the SARS‐CoV‐2 virus antigen, uncertainty surrounds their deployment and ultimate effectiveness in stemming infections. This article applies the analytic lens of biological citizenship (or bio‐citizenship) to explore Australia's experience of implementing a RAT‐based mass self‐testing strategy to manage COVID‐19. Drawing on Annemarie Mol's (1999, The Sociological Review, 47(1), 74–89) concept of ontological politics and analysing government statements, scientific articles and news media reporting published during a critical juncture of the strategy's implementation, we explore the kind of bio‐citizenship implied by this strategy. Our analysis suggests the emergence of what we call liminal bio‐citizenship, whereby citizens are made responsible for self‐managing infection risk without the diagnostic certitude this demands. We discuss how the different realities of mass self‐testing interact to reinforce this liminal citizenship and consider the implications for the sociology of diagnosis. [ABSTRACT FROM AUTHOR]

In this paper, I reflect on the experience of the Australian summer bushfires of 2019/2020 and the different ways forms of media reporting amplified its affects. Across broadcast media, local response, social media and personal account, I chart alternate stories during and after the event-as-spectacle. Taking into account the socio-political climate, the climatic atmosphere and the ongoing anxiety after the fires, I consider the use of apocalyptic words alongside the repetitive pairing of affective images to question what these might reveal about ourselves. Through the lens of affect attention is drawn to the many interacting conditions and forces that coalesce and gather as attachments, ideas, or assumptions and how these might influence perceptions of the event and actions in the aftermath of fire threat. Woven into the paper is my personal writing alongside details drawn from select Instagram accounts recording the everyday labours of caring for a place during and after the fires. As a counter-narrative to obliteration and all things lost, these missives disclose a different understanding of the event, long after the news media has moved on. For the authors and followers alike, lessons are revealed through attention to the land and hope in the processes of everyday encounters. [ABSTRACT FROM AUTHOR]

Introduction: Transvaginal mesh (mesh) surgeries have been used to treat stress urinary incontinence (incontinence) and/or pelvic organ prolapse (prolapse). In Australia, as in many other countries, the harms caused by mesh eventually prompted individual and collective attempts to achieve redress. The rise of mesh surgery as a procedure, the experience of mesh‐affected women and the formal inquiries and legal actions that followed all occurred in social, cultural and discursive contexts. One strategy to understand these contexts is to track how the mesh and key actors in the mesh stories have been portrayed in mass media sources. We conducted a media analysis of the most highly read Australian newspapers and online news media platforms, focusing on how mesh and the interaction of stakeholders in mesh stories were presented to the Australian public. Method: We searched systematically in the top 10 most‐read print and online media outlets in Australia. We included all articles that mentioned mesh, from the date of first use of mesh in Australia to the date of our final search (1996–2021). Result: After early scant media reporting focusing on the benefits of mesh procedures, major Australian medicolegal processes created a hook to shift reporting about mesh. The news media then played a significant role in redressing women's experienced epistemic injustice, including by amplifying previously ignored evidence of harm. This created an opportunity for previously unreported suffering to be revealed to powerful actors, in settings beyond the immediate control and epistemic authority of healthcare stakeholders, validating women's testimony and creating new hermeneutic resources for understanding mesh. Over time, media reports show healthcare stakeholders responding sympathetically to these new understandings in public discourse, contrasting with their statements in earlier media coverage. Conclusion: We argue that mass media reporting, in synergy with medicolegal actions and the Australian Senate Inquiry, appears to have provided women with greater epistemic justice, giving their testimony privileged epistemic status such that it was considered by powerful actors. Although medical reporting is not recognised in the hierarchy of evidence embedded in the medical knowledge system, in this case, media reporting appears to have contributed to shaping medical knowledge in significant ways. Patient or Public Contribution: We used publicly available data, print and online media outlets, for our analysis. Therefore, this manuscript does not contain the direct contribution of patients, service users, caregivers, people with lived experience or members of the public. [ABSTRACT FROM AUTHOR]

Background: Through the filtering of information, the creation, and reinforcement of stereotypes, media moulds attitudes and set agendas on critical social issues including public policy and disability. Methods: This study explored Australian media representations of the care of people with intellectual disability during a crucial period in disability policy change: the National Disability Insurance Scheme (NDIS) rollout (2013–2018). Search criteria identified 168 news stories, examined via content analysis and news framing. Results: Four major issues were identified: Roles and responsibilities of government; housing; mistreatment of persons with intellectual disability, and responsibility of care for families. Stories tended to be presented negatively, however, regional and local/community metropolitan stories were more balanced or positive compared with major metropolitan stories. Conclusion: Despite significant disability policy change, media presentations continue to reinforce stereotypes of people with intellectual disability and position the government as one continuing to fall short in critical areas of funding, safety, and support. [ABSTRACT FROM AUTHOR]

People receiving working-age income support payments are often stigmatised as morally and/or behaviourally deficient. We consider the role of the media, as a potential source of structural stigma, in perpetuating negative characterisations of people in receipt of either the Disability Support Pension (DSP) or unemployment benefits (Newstart) during a major period of welfare reform in Australia. Newspaper articles (N = 8290) that appeared in Australia's five largest newspapers between 2001 and 2016, and referenced either payment were analysed. We found an increased use of fraud language associated with the DSP, which coincides with increased political and policy focus on this payment. We conclude that in a period of increasing political concern with welfare reform, media coverage of welfare recipients is a form of stigma power, acting discursively as symbolic violence. [ABSTRACT FROM AUTHOR]

Background: Worry about climate change may be associated with poorer mental health but also with greater political engagement. We determined trajectories of climate change‐related worry over adolescence and whether these were associated with depression symptoms and greater engagement with news and politics in late adolescence. Methods: At ages 10–11, 12–13, 16–17 and 18–19 years, adolescents participating in the Kindergarten cohort of the Longitudinal Study of Australian Children rated their worry about climate change. At age 18–19 years, participants reported on depression symptoms and engagement with news and politics. Latent profile analysis determined trajectories of climate change‐related worry across all time points (N = 2244). Linear regression analyses examined the association between trajectories and outcomes at 18–19 years. Results: Thirteen per cent (n = 290) of adolescents had high persistent worry. The largest proportions had moderate (n = 559, 24.9%) or increasing worry (n = 546, 24.3%), followed by persistent low worry (n = 376, 16.8%), slightly decreasing worry (n = 297, 13.2%) and steeply decreasing worry (n = 176, 7.8%). Adolescents with high persistent worry had higher depression symptoms at age 18–19 years compared to the moderate group, while those with increasing worry did not. The high persistent and increasing worry groups reported greater engagement with news and politics across several measures. Conclusion: This is the first study to track climate‐related worry and outcomes in young people across adolescence. A substantial number of Australian adolescents experience high or increasing worry about climate change, which is associated with greater societal engagement. [ABSTRACT FROM AUTHOR]

Background: Selective dorsal rhizotomy (SDR) is a neurosurgical intervention to reduce spasticity in children with cerebral palsy. Parents researching SDR for their child may be influenced by framing of SDR in news media articles they read. This study examined framing of SDR in English‐language news media. Methods: Content analysis of English‐language news media articles including the search term 'rhizotomy' in the Factiva database published July 2015 to July 2018 in online or print form in Canada, New Zealand, Australia, United States of America and the United Kingdom. Results: One hundred and eighty‐six articles were identified describing 91 different children (45 male), almost all with cerebral palsy, median age 4 years old. One hundred and twenty‐six articles were written prior to surgery; in many articles, SDR surgery involved travel overseas and/or fundraising. SDR was described universally in positive terms with little discussion of risks. Content of articles variably included the specialized nature of SDR, parental frustration with their local health system and their hope for positive outcomes. There was geographical variation in both numbers of articles and content. Conclusions: SDR is a common focus in cerebral palsy news media articles in some countries. Framing in these articles supports SDR as a beneficial and specialized procedure and may lead families to believe they need to work outside their local health systems. As news media are likely an important influence on families' attitudes to SDR, clinicians should be aware of this influence. [ABSTRACT FROM AUTHOR]

This paper examines the use of metaphors to construct Italian migration within the 1920s Australian press. Using a critical discourse analysis approach, the paper investigates the range of metaphors used to frame Italian migration, which were also applied to Asian migration in earlier decades. It finds that such metaphors were a racially coded means for constructing immigrant deviance and threat. It further finds that this threat construction was the means by which immigration restrictions were legitimised and the need to preserve White Australia reiterated. While there was some ambivalence as to the extent of danger posed by Italian immigration, the use of such metaphors to frame discussion illustrates the extent to which debates around Italian immigration were, at heart, anchored in ideas of race. [ABSTRACT FROM AUTHOR]