Sharon A. McGregor

Background: In this study, objects are used as a representation of relational wellbeing to help young refugees living in Norway, Scotland, and Finland to talk about important persons who make them feel well. At the time of this research, there is no known study that uses objects to facilitate narratives of how young refugees and members of their social networks generate relational wellbeing. Methods: Using a qualitative approach, young refugees participated in individual interviews about the objects they brought to art workshops to understand their experiences, feelings, and acts of wellbeing. Results: Treating each object as unique to the owner was powerful in revealing how relational wellbeing is experienced and expressed. There were overlaps in experiences and expressions of wellbeing, hence our themes of discussion: overlaps between old and new social ties; between time and space; and between the three constructs of relational wellbeing. Old ties were not forgotten; instead, they evolved to a different form, supporting young refugees from a distance, while new ties contributed to what is needed in their present and at their current age. Experiences of relational wellbeing transcended time and space between their disrupted places of origin, their experiences on the journey, and settling in their new countries. The constructs of relational wellbeing—feeling good, being connected, and having enough—were inseparable in the participants’ experiences. Conclusions: We conclude that these overlaps have implications for a relational wellbeing approach in theory and practice. The results leave a challenge for both researchers and practitioners to develop complex research and intervention methods that can capture these tapestries of young refugees’ experiences of relational wellbeing.

In this article, we explore the role of family-like relationships in creating wellbeing for unaccompanied minor refugees (UMRs) to Europe. Our theoretical point of departure is a relational approach to wellbeing as conceptualized by Sarah C. White. The data comprises interviews with 51 settled UMRs in Finland, Norway, and Scotland, focused on their social networks, and a selection of paired interviews with young people alongside someone they defined as family-like and important for their wellbeing today. Findings illuminate the important role family-like relationships have in meeting the daily needs of young refugees. These relationships are ascribed meaning in the context of young people’s wider networks and ideas of ‘what family should do’. Family-like relationships gain particular importance for UMRs in two different ways: first, the physical absence of the family of origin enforces children and young people’s need to create trusted, reciprocal networks. Second, building family-like relationships is necessary in a new country where UMRs grow up and face new expectations, needs, and opportunities. We argue that relational wellbeing is built in a hybrid ‘third space’. A welfare state should support the wellbeing of UMRs by nurturing welcoming communities and providing UMRs help with building family-like relationships through formal and other support networks.

People with an intellectual disability experience high levels of social exclusion and a range of health inequalities. Increased inclusion and participation in healthcare decision making have been identified as key to promoting inclusion in health and social care. However, achieving these objectives requires increased recognition of the communication and health literacy needs of individuals with an intellectual disability and consideration of the appropriateness of the information currently provided. In this article, we report the results of a pre-COVID-19 qualitative study exploring the provision and use of accessible information to support the healthcare inclusion of individuals with an intellectual disability. A total of 35 clinicians participated in focus group discussions, and 10 people with intellectual disabilities and 10 carers were interviewed regarding their experiences of using accessible health-related information. Qualitative data analysis using a framework approach highlighted the crucial role of communication partners when using accessible information, deficits in current National Health Service (NHS: UK’s publicly funded health care system) information provision in the UK, and possible broader relevance of accessible resources. The implications of these findings for the provision of accessible information in a post-COVID-19 environment are explored, and recommendations are made for the increased integration and theory-driven research to inform the provision, content, and use of health-related information, especially the provision of online information, in the future.

Background: Evidence suggests that parents with intellectual disabilities can be “good enough” parents with appropriate support that focuses on the whole family. This paper brings together theories of vulnerability with an ethics of care approach to reflect on challenges for practitioners in supporting parents, drawing upon data from a study carried out in Scotland.Method: An online survey was administered to practitioners in three settings, and follow‐up interviews were carried out with key informants.Results: Pockets of good practice existed but a number of barriers to supporting families remained. These related to a lack of accessible information, difficulties in identifying and engaging with families at an early stage and poor joint working across agencies.Conclusion: The study concludes by arguing that practitioners' constructions of families as “vulnerable” reflects negatively on their perceived capacity to parent, creating further barriers in accessing appropriate support and reducing expectations of success.

Epilepsy is a serious medical condition that can have profound psychosocial effects. These effects can be minimised through self-management, but information about epilepsy can be complex and it can be difficult for people, especially those with learning disabilities, to understand and manage their condition. This group of people already experiences barriers to health literacy and the lack of accessible epilepsy information can further compromise ability to self-manage the condition. This article explores the existing literature relating to how people with learning disabilities are supported to understand their epilepsy, with particular focus on the effect of accessible information and education. Although research in this area is developing, it is limited, which therefore reduces the extent to which services can confidently use resources underpinned by evidence-based research.