Occupational health and safety of migrant sex workers in New Zealand

This research provides an in-depth understanding of issues facing migrant sex workers in New Zealand, with a particular focus on occupational health and safety, and sexual reproductive health. It was intended that the research would provide an evidence base from which NZPC could develop and provide migrant-relevant advocacy and services. Specific research objectives include: 1. understand the New Zealand sex work context in which migrants are working 2. identify the specific needs of migrant sex workers with regards to: occupational health and safety needs; sexual and reproductive needs; and any other needs that may contribute to the general health of migrant sex workers 3. identify barriers and facilitators to migrant sex workers\u27 receipt of appropriate services and/or required assistance

Ableism, human rights, and the COVID-19 pandemic : healthcare-related barriers experienced by deaf people in Aotearoa New Zealand

The COVID-19 pandemic significantly affected global healthcare access and exacerbated pre-pandemic structural barriers. Literature on disabled people’s experiences accessing healthcare is limited, with even less framing healthcare access as a human rights issue. This study documents and critically analyses Deaf people’s healthcare access experiences in Aotearoa New Zealand during the COVID-19 pandemic. Eleven self-identified Deaf individuals participated in semi-structured videoconferencing interviews. Discourse analysis was applied to participant narratives with discourses juxtaposed against a human rights analysis. Barriers influencing healthcare access included: (1) the inability of healthcare providers to communicate appropriately, including a rigid adherence to face mask use; (2) cultural insensitivity and limited awareness of Deaf people’s unique needs; and (3) the impact of ableist assumptions and healthcare delaying care. Barriers to healthcare access represent consecutive breaches of rights guaranteed under the United Nations Convention on the Rights of Persons with Disabilities (CRPD). Such breaches delay appropriate healthcare access and risk creating future compounding effects. Action is required to address identified breaches: (1) The CRPD should also underpin all health policy and practice development, inclusive of pandemic and disaster management responsiveness. (2) Health professionals and support staff should be trained, and demonstrate competency, in Deaf cultural awareness and sensitivity

‘It has totally changed how I think about the police’: COVID-19 and the mis/trust of pandemic policing in Aotearoa New Zealand

In the initial phase of COVID-19, Aotearoa New Zealand was internationally praised for its pandemic response that included lockdowns to control the spread and work towards elimination. Community compliance with control measures was thus essential when pursuing elimination as a policy. Using a mixed-methods approach, we sought to explore whether New Zealand Police (NZP) were trusted to police the lockdown rules at Levels 4 and 3. We analyzed 1,020 survey responses comparing trust among respondents who had been stopped by NZP over the lockdown rules (contacts) with those who had not (non-contacts). We found that both contacts and non-contacts expressed greater trust in NZP to enforce the Level 4 than the Level 3 rules; contacts expressed less trust in NZP to enforce the lockdown rules than non-contacts; contacts perceived NZP more heavy-handed than non-contacts; contacts perceived NZP as only somewhat procedurally just and feeling somewhat encouraged to comply with the lockdown rules and; that unexpected high-profile policing-related events during the survey only affected contacts’ trust significantly. We offer two explanations: (1) NZP were perceived as procedurally unjust or inconsistent in applying the lockdown rules, (2) members of the public and NZP learned the lockdown rules simultaneously. We caution that the unfamiliar character of pandemic policing may jeopardize trust in NZP even among segments of the population that typically express high levels of trust in NZP, i.e., people of European descent. We conclude that community compliance with pandemic control measures is no matter to be dealt with by the criminal legal system

The most difficult time of my life or ‘COVID’s gift to me’? Differential experiences of COVID-19 funerary restrictions in Aotearoa New Zealand

In 2020, the government of Aotearoa New Zealand imposed some of the most stringent funerary restrictions in the world as part of its efforts to eliminate COVID-19. This article explores how people experienced this situation, asking why restrictions that some described as precipitating ‘the most difficult time of their lives’ were described by others as a ‘relief’, ‘blessing’, or ‘gift’. Much existing literature frames funerary restrictions as a distressing assault upon established ways of grieving to which mourners must try to adapt–and in Aotearoa, both the stringency of the restrictions and the means by which they had been imposed did lead to many people finding them challenging. However, for those with ambivalent pre-existing feelings regarding their funerary traditions–such as many in the Samoan diaspora–COVID-19 restrictions afforded both a reprieve from burdensome practices and a much-welcomed opportunity to reimagine their traditions. Funerary restrictions, though disruptive, are thereby shown to have generative potential

Lockdown Ibuism: experiences of Indonesian migrant mothers during the COVID-19 pandemic in Aotearoa New Zealand

Lockdowns imposed to curb the spread of COVID-19 have been widely shown to heighten care burdens within households and ‘bubbles.’ Responsibility for meeting such burdens often falls disproportionately upon women. It is nevertheless important for research on gendered inequalities during COVID-19 to attend to the particularities of how such care work was experienced by differently positioned women. In Aotearoa New Zealand, Indonesian migrant mothers’ experiences of lockdown were mediated by the disadvantages they faced as ‘non-native’ speakers of English, as well as by the ideology of Ibuism (‘motherism’) they were socialised into during their lives in Indonesia. This socialisation led many to find life under lockdown life both rewarding and stressful in ways distinct from other women and mothers in Aotearoa New Zealand who were confronting similar demands. We thus argue for the importance of a qualitative and intersectional approach

Long-Distance Signals Are Required for Morphogenesis of the Regenerating Xenopus Tadpole Tail, as Shown by Femtosecond-Laser Ablation

tadpoles has recently emerged as an important model for these studies; we explored the role of the spinal cord during tadpole tail regeneration.Using ultrafast lasers to ablate cells, and Geometric Morphometrics to quantitatively analyze regenerate morphology, we explored the influence of different cell populations. For at least twenty-four hours after amputation (hpa), laser-induced damage to the dorsal midline affected the morphology of the regenerated tail; damage induced 48 hpa or later did not. Targeting different positions along the anterior-posterior (AP) axis caused different shape changes in the regenerate. Interestingly, damaging two positions affected regenerate morphology in a qualitatively different way than did damaging either position alone. Quantitative comparison of regenerate shapes provided strong evidence against a gradient and for the existence of position-specific morphogenetic information along the entire AP axis.We infer that there is a conduit of morphology-influencing information that requires a continuous dorsal midline, particularly an undamaged spinal cord. Contrary to expectation, this information is not in a gradient and it is not localized to the regeneration bud. We present a model of morphogenetic information flow from tissue undamaged by amputation and conclude that studies of information coming from far outside the amputation plane and regeneration bud will be critical for understanding regeneration and for translating fundamental understanding into biomedical approaches

The politics of gang research in New Zealand

Like many other Western jurisdictions over the past sixty years, New Zealand has had to contend with episodes of moral panic regarding the activities of youth gangs. The most recent episode occurred in 2005-2007 and was spurred by a perceived escalation in inter-gang conflict and violence in the Counties Manukau areas within greater Auckland, New Zealand. This particular episode was unique in the New Zealand context for the level of attention given to youth gangs by the government and policy makers. This paper reports on the authors’ experiences of carrying out research on the youth gang situation inCounties Manukauas part of an inter-agency project to develop a response to gang-related violence. Particular attention is paid to the ways in which government officials attempted to mould the research process and findings to suit an already emerging policy framework, predicated on supporting ‘business as usual’, at the expense of research participants calls for great autonomy to develop and delivery appropriate youth services to their communities

Key issues effecting field researcher safety: A reflexive commentary

This article raises concerns about the, arguably, obscure position the issue of field researcher safety holds in our training curricula, supervision processes and across our research communities. A variety of discursive tensions are discussed as preventing a full realisation of researcher safety as a significant issue for social research practitioners. These tensions include the impact of privileging violence over the wide range of risks inherent in researching the social context, the ideological construction of the intrepid researcher as someone who bravely enters the field, often without an understanding of the environment or cognisant of potential risks; thus relying on a combination of courage and wit to develop an understanding of the issues under investigation. A third tension arises out of the elevated position afforded participant safety in the discourse on research safety. A hierarchy of issues has constructed researcher safety as a lesser concern to that of participants and (importantly) institutions. Next, decreases in researcher safety are discussed in relation to efforts to gain participant rapport and the impact of marginalised status on our safety as researchers. Finally, various organisations and workplaces\u27 risk adverse approaches to safety are presented as superficial institutional tasks that provide minimal safety to the individual while providing the organisation with maximum protection

The experience of accessing healthcare for people with rare disorders

Rare disorders (RDs) are classified as low-prevalence health conditions (1); however, collectively, 6% of the world's population have a least one diagnosed RD; this reflects the prevalence of RDs in Aotearoa New Zealand. Amongst this population, approximately 50% are children (2). Given issues with diagnosing RDs, the true prevalence may be considerably higher. Similarities across RDs include the involvement of multiple medical specialities, body sites, condition chronicity, limited treatment options, and certain psychosocial risk factors. The burden of having a RD is high, resulting in concomitant disability and additional health and disability service need (3, 4). This scoping review will examine the impact of healthcare access and delivery on those with a diagnosed RD

Wellbeing for older adults in Aotearoa/New Zealand Vision for Ageing in Aotearoa.

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