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We used mixed methods to learn about the nature and drivers of mental health changes among autistic adults in the United Kingdom during the early stages of the COVID-19 pandemic. In quantitative analyses, we examined the nature and predictors of change in depression, anxiety and stress, prospectively measured in 70 autistic adults at Wave 1 (just before the United Kingdom’s first lockdown) and Wave 2 (10–15 weeks into the United Kingdom’s first lockdown). Retrospective Wave 2 reports of mental health change were also analysed for these 70 participants. For the qualitative analysis, 133 participants (including the 70 from the quantitative analyses) provided reports on their experiences of the pandemic at Wave 2. In quantitative analyses, retrospective reports indicated that participants’ mental health worsened, but prospective data showed a different picture, with overall anxiety and stress scores reducing between Waves 1 and 2. Nevertheless, the mental health impact of the pandemic on autistic adults was variable, with a sizable minority reporting a significant decline in mental health. Qualitative analysis yielded four themes that contributed to mental health changes: (a) adjusting to changes to the social world, (b) living with uncertainty, (c) disruptions to self-regulation, and (d) barriers to fulfilling basic needs. Lay abstract During the COVID-19 pandemic, high levels of depression, anxiety and stress have been reported in the general population. However, much less has been reported about the impact of COVID-19 on the mental health of autistic people. What we did: In the present study, we investigated how the mental health of autistic adults in the United Kingdom changed during the early stages of the COVID-19 pandemic. In total, 133 participants completed an online survey at two different time points. Of the 133 participants, 70 completed the survey at the first time point just before the onset of the national lockdown. This allowed us to look at changes in their mental health, from before the lockdown to 10 to 15 weeks during lockdown. All participants (133) told us about their experiences of the pandemic. What we found: While many autistic adults told us that their mental health worsened, people’s experience varied. For some autistic adults, aspects of mental health (e.g. anxiety, stress) actually improved. Participants also described social changes that had occurred, at home and in the outside world. They described feelings of uncertainty during the pandemic, and discussed how the pandemic had affected some of their previous coping strategies. Participants also told us about their difficulties in accessing healthcare services and food during the early stages of the pandemic. In our article, we discuss these findings and focus on what needs to change to ensure that autistic people are better supported as the pandemic continues.

While Australia has experienced low COVID-19 case numbers relative to other countries, it has witnessed severe economic consequences in the wake of the pandemic. The hospitality industry, in which young adults are overrepresented, has been among the most affected industries. In this article, we present findings from an interview and a digital methods-based study of young hospitality workers in the Australian cities of Melbourne and Newcastle who lost shifts or employment due to the pandemic. We argue that the participants’ ability to cope with the loss of work was mediated by the degree of family support that they could access, with some experiencing the pandemic as an inconvenience, while others suffered extreme financial hardship. Findings from this study show that the most severe impacts of the pandemic play out along pre-existing lines of inequality and marginality, causing the most severe consequences for those who were already most vulnerable to them.

Mild cognitive impairment (MCI) is a concept that is steeped in controversy not limited to prognostic uncertainty; it is unclear how patients interpret or attribute meaning to the label, and whether they perceive that being made aware is beneficial.A systematic review was conducted, searching ISI Web of Science, PubMed and PsycINFO in accordance with PRISMA guidelines. Search terms were developed to include articles concerning perceptions regarding MCI and experiences and impact of being informed. Thematic synthesis was applied to the findings.Fourteen papers met criteria. Three themes emerged regarding the MCI label: 1) Individual differences relating to living circumstances, personal perceptions and experiences, and coping style affect how patients adjust to the MCI label; 2) Patients' reactions to the MCI label and their perceptions about how useful it was to receive are affected by the nebulous nature of the construct and information available regarding MCI; 3) Care partners are uncertain about what MCI means and how to address and cope with the patient's cognitive difficulties.Patient and care partner perspectives were affected by the quality of information and support provided, possibly influenced by clinicians' understanding of the concept. Personal perceptions and experiences, living circumstance and coping styles also shaped experiences of being informed.Clinicians should develop their understanding of MCI to deliver clear information to patients and consider the necessity of applying the label. Offering support tailored to patients' specific needs may improve perceptions about the label's utility, whilst aiding coping and adjustment.

Newspaper media plays a significant role in forming a public understanding of domestic violence. This article analyses 554 articles from 24 newspapers across Australian states and territories published between 2000 and 2020 that describe specific instances of domestic violence. It examines whether such violence is framed as a systemic issue or as a collection of individual events, as well as how such representations of perpetrators and victims displace both “blame” and “victimhood.” Although positive aspects of reporting can be observed, the tendency within newspaper articles to blur distinctions between perpetrators and victims distorts the true scale of domestic violence in Australia.

Research considering young adults’ experiences of place is characterised by two focal points: the relationship between place, education and employment; and immaterial aspects of place such as experiences of belonging and relationality. Previous research has worked across these focal points considering, for instance, how symbolic and immaterial factors and social ties can inform mobility choices and experiences. We extend this work by drawing on longitudinal qualitative data to show three ways that place attachment can be a part of the formation of contemporary occupation-based identities. Using the concept of the self as enterprise (Kelly 2013), we mark out this development as part of a broader generational shift in occupational identities. We ultimately find that some young adults can remain in or return to meaningful rural and regional places by developing an occupational identity or ‘personal brand’ informed by changing occupational demands and enabled by social ties linked to specific places.

Research considering how time is organised has shown that women tend to carry a disproportionate burden of coordinating the schedules of their households. However, little research has considered how these gendered inequalities may manifest in the context of the shift away from ‘standard’ work patterns and towards variable and non-standard hours. We address this question by using interview and digital data to consider how a selection of ‘ordinary’ Australian young adults in heterosexual partnerships manage and coordinate their time. We contend that even for middle-class young adults with relatively high employment security, increasingly complex working arrangements are shifting existing inequalities in gendered divisions of temporal labour in ways that heighten feelings of temporal insecurity. We conceptualise our findings as part of an intensification of the existing need to schedule and manage lives that is widely felt in the so-called ‘gig economy era’, even by those removed from gig work proper.

Although humanities and social science disciplines have witnessed an explosion of interest in the topic of hope in recent decades, uptake of this concept has been comparatively uneven in sociological research. Hope has garnered substantial attention in relation to topics such as health, poverty, youth and work within creative industries, while attracting sporadic interest elsewhere. However, despite this uneven engagement, studies addressing hope in each area have echoed many of the same ambiguities. We focus on two such ambiguities: the relationship between hope and futurity, and the relationship between hope and agency. Drawing on the observation that recent treatments of hope appear to either emphasise a hoped-for outcome situated in the future or focus on the role of hope in coping with the present we reframe this debate, contending that these tendencies suggest two distinct modes of hope: representational and non-representational. By reframing the relationship between hope and futurity thus we seek to, in turn, untangle the ambiguous relationship between hope and agency. We test the utility of our conceptualisations of hope by placing them into dialogue with longitudinal case studies compiled from biennial interviews and annual surveys conducted over a 10-year period. We ultimately put forward some means by which recent sociological treatments of hope can be unified, and in so doing contend that conceptualising hope not as an individual experience, but as part of broader political economies of hope can attune us to the ways in which inequalities are manifest through uneven distributions and experiences of hope.

Recent years have witnessed an explosion of interest in hope in the disciplines of sociology and anthropology. Although expressions of hope on varying scales have been considered, this article focuses on recent scholarship addressing micro, often individual experiences of hoping. Such experiences of hope dovetail with a recent strand in utopian studies focusing on material and practice-based considerations and drawing utopian energies into everyday life. Working between these points of homology, this article considers the relationship between small-scale expressions of hope and utopian thinking. Literature addressing diverse subject matter is compared on the basis of its conceptualizations of hope. The outcome is twofold. First, common understandings of hope are identified in research addressing diverse topics. Second, Darren Webb's typology of modes of hope and their relationship to utopian thinking is expanded upon, and ultimately, a dichotomous understanding of modes of hope as either utopian or anti-/non-utopian is challenged.

Numerous studies have found that although young adults are arguably less constrained by gendered norms and expectations than previous generations, they have nevertheless continued to imagine their ...

Sociological work has often characterized the contemporary future horizon as a space crowded with risks and contingencies. This view has prompted a number of claims that young adults conceptualize the future predominantly in terms of the choices and plans that they make to mitigate against such concerns. As an extension of this logic, a number of studies have suggested that young adults conceptualize the long-term future extending beyond their own lives separately from their more immediate horizon of planning (Leahy et al., 2010; Toffler, 1974 ). This paper discusses how young adults relate to the long-term and more immediate future concurrently, and in doing so considers the points at which the strategies that they use to cope with contingency in their own lives may intersect with the ways that they approach their fears, hopes and imaginings of the long-term future. The data for this paper are drawn from an interview project in which young adults (aged 18–34) were asked to discuss their own futures, and a general idea of the future. The findings are used to form the beginnings of a typology of the approaches that young adults may adopt when engaging with the future, which is then drawn upon to propose that the ways in which they engage with the long-term future are often related to the strategies that they employ when facing their own futures.

Individuals with attention-deficit/hyperactivity disorder (ADHD) often grow up with negative messages surrounding their abilities and may experience adverse outcomes throughout their lives. Despite this, by adulthood, those with ADHD often find that they are left without adequate support from services. This review explores the relationship between self-esteem and ADHD in adulthood with a view to outlining needs and potential opportunities in terms of service provision. Twelve databases were searched for relevant literature published between 1980 and 2013 using terms relating to self-esteem, ADHD and adulthood. The resulting 13 articles comprised both cross-sectional and intervention studies. Despite a limited number of studies and methodological concerns, there is evidence to suggest that ADHD is associated with lower self-esteem in adulthood and that self-esteem difficulties can be remedied, to at least some extent, by psychotherapeutic work. It is recommended that future research focuses on the evaluation of therapy that specifically targets difficulties in self-esteem in this population.

Purpose – The paper aims to highlight the contributions and opportunities offered by an ageing society to their local communities and wider society.Design/methodology/approach – The paper is set out in six sections: an overview of WRVS; challenges of an ageing society; the “grey pound”; provision of social care; volunteering and non‐financial and other contributions of older people. This paper draws on research published by WRVS in March 2011 while providing more detail on the contribution of, and opportunities for, older volunteers with supporting case studies.Findings – The paper shows the benefits of an ageing population, the contributions currently made by the UK's pensioners, and the inevitable increase in their provision to society.Social implications – In the UK, over 65s are often seen as a burden on society's resources. In many other cultures older people have an elevated status and respect. Older people make a huge contribution to the UK's society but their potential is not always realised. This...

Lichen sclerosus (LS) is considered to have an immunogenetic background. Several small studies, using serological typing, have reported that HLA-DR11, DR12, and DQ7 were increased in LS, with DR17 less frequent. This study aimed to validate and detect new HLA-DR and DQ associations with LS in females and its characteristic clinical parameters. The cases, 187 female LS patients, and 354 healthy controls were all UK North Europeans. PCR-sequence specific primers method was applied to genotype the HLA-DR, DQ polymorphisms that correspond to 17 serologically defined DR and seven DQ antigens. Statistical analysis was performed with two-tailed Fisher's exact test with Bonferroni adjustment (p value after Bonferrroni adjustment, Pc). We found increased frequency of DRB1*12 (DR12) (11.2%vs 2.5%, pc0.01) and the haplotype DRB1*12/DQB1*0301/04/09/010 (11.2%vs 2.5%, p0.001, pc0.05), and a lower frequency of DRB1*0301/04 (DR17) (11.8%vs 25.8%, pc0.01) and the haplotype DRB1*03/DQB1*02DRB1*0301/DQB1*0201/02/03 (11.2%vs 24.6%, pc0.0001) in patients compared with controls. HLA DR and DQ antigens were not associated with time of onset of disease, site of involvement, structural changes of genitals, and response to treatment with potent topical steroids. In conclusion, HLA-DR and DQ antigens or their haplotypes appear to be involved in both susceptibility to and protection from LS.

Lichen sclerosus (LS) is considered to have an immunogenetic background. Several small studies, using serological typing, have reported that HLA-DR11, DR12, and DQ7 were increased in LS, with DR17 less frequent. This study aimed to validate and detect new HLA-DR and DQ associations with LS in females and its characteristic clinical parameters. The cases, 187 female LS patients, and 354 healthy controls were all UK North Europeans. PCR-sequence specific primers method was applied to genotype the HLA-DR, DQ polymorphisms that correspond to 17 serologically defined DR and seven DQ antigens. Statistical analysis was performed with two-tailed Fisher's exact test with Bonferroni adjustment (p value after Bonferrroni adjustment, Pc). We found increased frequency of DRB1*12 (DR12) (11.2%vs 2.5%, pc