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The special issue, “Meeting Global Challenges through Families and Community Environmental and Sustainability Education: Generating Action Competence” aims to discover and address ways of meeting global educational and political challenges of sustainable futures from the perspective of families and community involvement. With contributions from multiple disciplinary and multidisciplinary fields it is organised around four thematic areas. Namely, Education for Empowering Communities for Change through Climate and Cultural Heritage; Families and Communities Educating for Sustainable Futures; Interdisciplinary Approaches to Education for Building Resilience in the face of Environmental Complexity and Uncertainty; and Integrating Methodologies for Researching and Developing Action Competence for Environmental and Community Sustainability through Education.
Collaboration is essential to inclusive practice, ensuring that children with disabilities, developmental differences and neurodivergence receive holistic, coordinated and high-quality support. A collaborative, team-based approach allows children to experience inclusive, responsive learning environments where interventions are seamlessly integrated into their everyday experiences. Research has demonstrated that when educators, allied health professionals, and families work together, children’s learning and development are enhanced, leading to greater participation, engagement and wellbeing.
The voyages of Columbus and his successors linked the two hemispheres, and this chapter surveys the positive and negative biological, cultural, and social consequences of this “Columbian Exchange.” Among these were the spread of disease and the transfer of plants, animals, and consumer goods, along with economic changes that led to social protests, revolts, warfare, and forced migrations in an increasingly interdependent world. Religious transformations, including the Protestant and Catholic Reformations and the creation of Sikhism, were interwoven with all of these developments, as religions, too, migrated and morphed. New urban social settings and cultural institutions, such as coffee and tea houses, theatres, and salons, offered men—and sometimes women—opportunities for entertainment, sociability, consumption, and the exchange of ideas, but the increasing contacts among peoples also resulted in more rigid notions of human difference.
Food insecurity (FI) has increased in recent years due to economic shifts and rising food prices, with 13.6% of UK households experiencing FI, 47% including children in 2024. Following PRISMA guidelines, this systematic review with narrative synthesis explored the impact of UK interventions addressing FI for children, families, and pregnant women. Seven databases and two clinical trial registers were systematically searched for articles published between 2008–November 2023 (rapid search November 2023–February 2026). Peer-reviewed intervention studies were eligible if they were conducted in the UK, had an experimental design, targeted at least one FI pillar (accessibility, utilisation, availability, and stability) and if most participants were children aged 0–11 years, families with at least one child 0–11 years, or pregnant women. 18,225 articles were identified (rapid search identified 5,514); 11 intervention studies were included (rapid search n = 2). Types of interventions included cooking interventions (n = 4), free school meals (n = 3), holiday clubs (n = 2), supermarket vouchers (n = 1), and food bags (n = 1). Food availability was targeted in seven studies, food accessibility and utilisation in five, and food stability in one, one study included FI as an outcome. The interventions demonstrated barriers and facilitators to inform future intervention development. Most studies were considered serious or critical risk of bias. A lack of high-quality interventions addressing FI were identified. The additional studies reflected the evidence from the original studies. Government policies and funding are needed to relieve FI. Research needs to co-develop acceptable interventions and evaluate their effectiveness to reduce FI among families.
This study examined adolescent–family relationship predictors of adult-era resilience in the face of the COVID pandemic, considering both mental and physical health outcomes. Adolescents (99 female, 85 male; 107 White, 53 African American, 15 mixed race/ethnicity, 9 from other minority groups) were followed from age 18 to 38 utilizing both observational and self-report assessments. After accounting for levels of functioning pre-COVID, adolescents who demonstrated a capacity to handle disagreements without becoming engaged in relatedness-undermining hostile behavior in mother-adolescent dyads went on as adults to experience relatively fewer depressive symptoms and better physical health quality post-COVID onset (Direct β’s = 0.28 and −0.17, respectively). Follow-up analyses suggested these effects were potentially mediated by maternal reports of adult-era quality of the mother-participant relationship, by level of ongoing maternal contact, and by lower levels of loneliness. Evidence was also found that maintaining contact with fathers in adulthood predicted better health outcomes post-pandemic. Results are taken as supporting a systems approach to understanding resilience, as Luthar has suggested, and identifying the mother–adolescent relationship as a potential long-term protective factor well into mid-adulthood.
The family is rarely a topic of international politics, but politicised captivity is one of the few domains where familial relations can play a prominent role. Crucially, the families involved generally lack the traditional power resources of wealth or official status that would normally be understood to influence outcomes within international politics. What they do possess, however, is a different set of emotional–political resources that both evoke emotion and invoke a diverse set of social rules concerning emotional experience. To explore our claims, we examine the case of the family of Yokota Megumi, a thirteen-year-old Japanese girl abducted by North Korea. This case both illustrates the potential of emotional–political resources to mobilise action and also highlights the risks that emotional narratives of families can be leveraged by political actors for their own purposes.
The introduction presents the background to the writing of the book. The author is an experienced Guantanamo lawyer who represented many detainees, including the last two Kuwaiti detainees, and was asked by Kuwaiti colleagues and friends to tell the stories of the twelve Kuwaiti detainees their lives before Guantanamo, how they were captured, their torture and treatment at Guantanamo, how they came to be released, and how they have tried to rebuild their lives after their long ordeals. The Core Team is introduced, a Kuwaiti lawyer, Abdul Rahaman Al Haroun, an American lawyer, William Brown, both based in Kuwait, and their colleague in Washington, Marcia Newell. These three strategized and fought every day for fourteen years until the last of the Kuwaitis was released.
Having a child with a psychiatric diagnosis is associated with parents’ greater risk of subsequent mental disorders but no immediate change in their annual labour market metrics. This discrepancy could be explained by shorter absences from work. We examined first-time psychiatric sickness absences in parents whose children have psychiatric diagnoses.
Methods
Using several linked nationwide Finnish registers, in this cohort study we examined time to first psychiatric sickness absence in parents whose children were born in 2001–2012 (early-childhood-onset diagnoses) or 2005–2016 (late-childhood-onset diagnoses). Exposure was having a child with a psychiatric diagnosis. Follow-up started when the parent’s eldest turned 1 (early-childhood-onset diagnoses) or 5 (late-childhood-onset diagnoses) and ended at psychiatric sickness absence, emigration, 68th birthday, death, or 31 December 2020, whichever occurred first.
Results
The 2001–2012 and 2005–2016 cohorts included 357 135 and 397 874 parents followed for 3.31 and 3.70 million person-years. Having a diagnosed child was associated with greater risk of psychiatric sickness absence in all except men whose children had substance use or psychotic disorder diagnoses. Time-varying analyses showed the greatest associations for women (HR: 4.92; 95% CI: 3.97–6.10) and men (HR: 2.48; 95% CI: 1.61–3.80) within 6 months of a child’s eating disorder diagnosis.
Conclusions
Parents of children with psychiatric diagnoses may be at a greater risk of a psychiatric sickness absence. Associations differed by child’s diagnosis, parent’s gender and time since diagnosis.
In this chapter, we will look at how children play in families, and the diversity of roles that parents may take in children’s play. We begin this chapter with details of the play practices of two families living in the same community. We argue that play is learned in families, and in early childhood centres and classrooms, rather than being something that arises naturally within the child. Through reading this chapter on families at play, you will gain insights into how some families play and how play is learned in families, and an understanding that play practices learned at home lay the foundation of children’s play and learning, and that as teachers we should consider how to build upon these early experiences in our early childhood centres and classrooms.
In “Parental Love and Filial Equality,” Giacomo Floris and Riccardo Spotorno offer an explanation for why parents should treat their children as equals. The authors argue that this moral obligation is grounded in parents’ duty to love their children in an attitudinal, though not necessarily emotional, sense. This duty, they contend, requires them to disregard variations in their children’s status-conferring properties, as long as those properties meet a minimum threshold. This article argues that this account of filial equal treatment has serious shortcomings. In its place, it proposes a more outcome-oriented or consequentialist account.
This article analyzes the medicalisation strategies deployed by Peruvian alienists in the daily life of the Lima Asylum during the last third of the 19th century. Special attention is given to the process of hospitalisation of the insane in the psychiatric hospital, since this administrative procedure reveals the dialogue, confrontation, and negotiation between the asylum staff and the state and social bodies in the public management of insanity. Through the support of the civil authorities in charge of the psychiatric hospital administration, we argued that the local alienists sought to impose medical knowledge in the asylum space as the legitimate criterion for the confinement of the insane in Peru. This process was not without tensions, setbacks, and disputes, especially with the families and the state agencies of control and social defence seeking to preserve their former prerogatives over the fate of their insane. However, we propose that these medicalisation strategies promoted by the alienists in the daily space of the Lima Asylum managed to situate psychiatric care as a state problem and these actors as experts in the public management of insanity.
This chapter proposes new readings of the poems of Whym Chow: Flame of Love based on ideas of unconventional domesticity, alternative divinity, and queer, chosen families. The chapter explores the ways in which animal characteristics disrupt and subvert conventional poetic form and religious teachings in the volume, specifically elegy and Catholicism. It also focuses on connections between Michael Field’s writing and animal poetry found in the work of other fin-de-siècle and modernist writers. The chapter proposes that these poems can and should be celebrated for their eccentricity, oddity, and queerness rather than overlooked and marginalised within Michael Field’s oeuvre.
Un certain nombre d’articles et de chapitres d’ouvrages évoquent les remaniements fonctionnels des familles face à la maladie neuro-évolutive (MNE) d’un de leurs proches. Cependant, peu d’études s’arrêtent sur le vécu de ces familles, sur leur positionnement face à la maladie et de comment elles se sentent reconnues par leurs proches atteints d’une MNE à un stade sévère. Dans cette étude, nous nous sommes intéressés au sentiment de reconnaissance des enfants et des conjoints, aux émotions de colère et de tristesse ainsi qu’aux sentiments de découragement et d’impuissance vécus par les familles face à l’évolution de la MNE de leurs parents / conjoints. Nous avons souhaité savoir s’il existait une différence significative entre les enfants et les conjoints au niveau de leur sentiment de reconnaissance et de leurs vécus. Nos résultats montrent qu’il existe une différence significative entre les enfants et les conjoints au niveau de la colère.
This chapter considers the experiences of those emigrants who did not respond to the call to arms and thus became draft evaders. With few exceptions, evading the Italian draft was actually quite easy for emigrants and brought no immediate consequences. Draft evasion simply meant that a man would decline to present himself at the consulate to arrange the trip home. The chapter explores the factors that influenced men to evade the draft, including the impact of family members, economic concerns and political beliefs. Socialists and anarchists, in particular, were militant draft evaders: some even left the United States for Mexico in order to avoid call-up to either the Italian or American armies. Treaties were signed between Italy and Britain and France for the reciprocal exchange of draft evaders although Italians were the primary target of the policy, while in Australia Italian draft evaders were rounded up and deported so that they could be enlisted into the Italian Army.
This chapter traces the emigrant soldiers’ experiences after their arrival in Italy. For some, it was their first encounter with a country they had heard so much about and many had the opportunity to engage in sightseeing before enlistment. Others were devastated to be swept off to the front without having the chance to see their parents and families. Returning from abroad to comply with a mobilisation order did not confer any special status on the emigrant soldiers. Once at the front lines, the mobilised emigrants suffered the same privations, injuries and hardship as all other Italian soldiers and officers. One of the major issues for those from South America and North Africa was the unfamiliar cold and snowy conditions they experienced. Others were disappointed to be stationed away from the front and that their service was not as exciting as they had expected. However, depending on their place of residence abroad and, in some cases, their pre-war occupations and language skills, the fact of their emigration did impact on their physical experience of combat and warfare. The chapter details the emigrant soldiers’ combat experiences, including gas attacks, the rout at Caporetto in 1917 and internment as prisoners of war.
Across Australia and beyond, early childhood education (ECE) services play a significant role in the everyday lives of infants, toddlers and their families. For some decades, the enrolment of infants and toddlers has increased to the extent that, in today’s Australian society, around 40% of birth to 24-month-olds and nearly 60% of two-year-olds spend at least part of their week in an early childhood service. More still balance ECE service attendance with informal care arrangements with family members and friends. With these figures echoed across many countries worldwide, the widespread uptake of infant and toddler early childhood programs has meant that this generation of infants and toddlers and their families are experiencing a markedly different start to life than previous generations. It is now the norm for infant–toddler care to be spread across multiple contexts both within and outside of the walls of the family home, and for the responsibility for early learning to be shared between family and non-familial adults.
This chapter reflects on the future of family law in an era of longer lives. Our analysis leads us to conclude that the 100-year life is indeed likely to have an impact on the nature, scope, and definition of family law, but that families will continue to function as the primary setting for intimacy and for caregiving and caretaking, whatever form those families take. Further, the importance to both individual and social welfare of family support throughout life points to a need for reform of current family law doctrine. The impact of longer life on doctrines regulating the relationship of parents and minor children is likely to be modest, but doctrinal and policy reforms will be needed to support individuals in following their preferences for intimacy and security in old age -- as will reforms to the minimal role of the state in promoting security for individuals in different family forms and of differing socioeconomic status. We suggest general goals for law reform and offer specific proposals.
The health and well-being of families is an important consideration for federal, state, and/or local levels of government. Family health policies based on recent knowledge of early childhood development have evolved to emphasise the importance of providing every child with the best possible start to life. Childhood sets the foundation for future health and well-being and is recognised by the 1979 United Nations Convention on the Rights of the Child. To impact health inequalities, government policies and services must address the social determinants of early child health, development and well-being.
Comprehensive planning for family reunification following a disaster is complex and often underdeveloped, especially in hospitals. The 2013 and subsequent 2021 National Pediatric Readiness Project revealed less than half of hospitals had disaster plans that addressed the needs of children. Leveraging quality improvement (QI) language and methodology allows for alignment and engagement of hospital leaders and personnel unaccustomed to disaster planning. We aimed to create a family reunification plan which would enable child-safe reunification within 4 hours of an event using quality improvement methodology. QI tools such as the fishbone diagram, key driver diagram, and process maps enhanced the planning process. We then utilized the Plan-Do-Study-Act model to test and revise our plan. Active involvement of key stakeholders was crucial. By using quality improvement methodology, hospital personnel unfamiliar with disaster management helped develop and improve our hospital’s family reunification plan.
Edited by
James Ip, Great Ormond Street Hospital for Children, London,Grant Stuart, Great Ormond Street Hospital for Children, London,Isabeau Walker, Great Ormond Street Hospital for Children, London,Ian James, Great Ormond Street Hospital for Children, London
Anaesthetists working in paediatric settings may care for patients ranging in age from preterm neonates to teenagers, some of whom will be undergoing relatively simple procedures for isolated conditions whereas others will have extremely complex needs and will be undergoing complicated, high-risk procedures. What all of these patients will have in common, however, is the need for developmentally appropriate communication from and with the professionals caring for them. Alongside an understanding and knowledge of the anatomical, physiological and pharmacological issues relevant to the care of the paediatric patient, anaesthetists also need an understanding of the developmental, communication, emotional and behavioural issues relevant to their paediatric patient. This chapter summarises some of the key theories of cognitive and psychosocial development, including beliefs about illness, and how these are relevant to the child undergoing anaesthesia. Effective communication with children and their families is central to the delivery of high-quality care, and this is discussed alongside the role of preparation and behavioural and psychological techniques in optimising experiences and outcomes for the child, family and anaesthetist.