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The Equality Act provides protection against discrimination on the ground of various protected characteristics: sex, race, disability, age, religion and gender. It protects against direct discrimination where there is adverse treatment because of a protected characteristic, and also indirect discrimination where the same rule is applied to all groups but has an unjustified and disproportionate adverse effect on a group. Adverse treatment includes harassment and victimisation. There is in addition a duty of reasonable accommodation for disabled workers. The law also requires equal pay for women for similar work or work that has equal value to that performed by men.
This introduction sets out a few overarching themes: Hemingway as a restlessly experimental writer, one driven to represent an ever-greater range of human experience and expression. Hemingway’s pressing against the boundaries of readers’ taste and tolerance is introduced, as is his identity as a person who lived with both visible and invisible disabilities and treated the ways of being in the world specifically available to the disabled.
The chapter provides an overview of Hemingway’s life from his birth in Oak Park, Illinois, to his death in Idaho. Key episodes include his experience, including his wounding, during the First World War, his emergence as a writer in Paris in the 1920s, his travels in Europe and Africa, including as a war correspondent during the Spanish Civil War and the Second World War, and his receipt of the Nobel Prize for literature.
The civil war in Spain provoked deeper political thinking and involvement for Hemingway, and his political engagement shaped his writing about that war. Hemingway returned to his journalistic roots in the war reportage he wrote on the conflict, and experimented with dramatic form in his only play, The Fifth Column. In For Whom the Bell Tolls he absorbs, adapts, and rejects a romanticized view of the Spanish Civil War that had been developed and promulgated by European and American writers sympathetic (as Hemingway was) to the Spanish Republican cause, stripping from the realities of internecine conflict any potentially consoling significance of political commitment. The Second World War also drew Hemingway as a war correspondent (initially reluctant, he became an enthusiastic witness to, and even participant in, combat in France and Germany). On the basis of his wartime experience, he explored themes of forgiveness and grace in Across the River and into the Trees, a flawed novel whose purgatorial narrative is nevertheless an interesting experiment in fictional form.
This chapter follows Hemingway from his journalistic work in the early 1920s through the publication of The Sun Also Rises in 1926. Ambitious to write fiction that would be innovative and popular, Hemingway absorbed the influences of Sherwood Anderson, Ezra Pound, Gertrude Stein, and others as he adapted news stories into sketches and wrote short stories based on combat experience and on his youth. Hemingway’s early style grew in the rich soil of literary experimentation in Paris in the 1920s, where he encountered an international literary and artistic avant-garde. This earliest work exemplifies Hemingway’s experimentation and its relationship to his deep need to express the apparently inexpressible contents of his psyche and experience. The reception of his 1925 story collection In Our Time established his early reputation. This chapter’s reading of The Sun Also Rises emphasizes Hemingway’s ironic deployment of both received narrative conventions and religiously significant pilgrimage and ritual themes, which locates Hemingway in a crucial vein of literary modernism exemplified by Eliot’s The Waste Land. Like these other modernist works, Hemingway’s novel is immured in the social attitudes within which he worked; anti-Semitism, racism, and homophobia tangle the novel’s surface texture but also shape its narrative structures.
Over the last five years of the 1920s, Hemingway worked assiduously to consolidate his reputation, publishing stories in mainstream magazines and developing what would become a lifelong relationship with the Charles Scribner publishing company. He worked to balance literary experimentation and innovation in the short story and the novel (sometimes courting censorship by challenging the canons of “decency”) and to appeal to popular taste. His second collection of stories includes the classic “Hills like White Elephants,” a powerfully concise exploration of power dynamics and competing visions within a romantic relationship. In A Farewell to Arms, Hemingway brings a corrosive irony to the topoi of the wartime romance, complicating received notions of both martial heroism (the military centerpiece of the novel is a shambolic retreat) and heterosexual romance (suggested in Frederic Henry’s and Catherine Barkley’s repeated references to wanting not only to be with one another but to be one another). The novel also sees Hemingway experiment with new modes such as stream-of-consciousness narration.
One hundred years after the publication of his first major work, Ernest Hemingway remains an important author. His work addressed the search for meaning in the wake of a 'Great War' and amid the challenges of rapidly changing social conventions, and his prose style has influenced generations of journalists and writers. Hemingway was wounded on the battlefield and caught up throughout his life in conflicting desires. He was also a deeply committed artist, a restless experimenter with the elements of narrative form and prose style. This book's detailed discussions, informed both by close formal analysis and by contemporary critical frameworks, tease out the complexity with which Hemingway depicted disabled characters and romantic relationships in changing historical and cultural contexts. This introduction is especially useful for students and teachers in literary studies and modernism.
1. What does the term ‘healing journey’ mean to you? 2. In what ways do you currently feel social work is both a gift and a burden? 3. What lessons does Gloria’s story teach us about who is responsible for what? 4. What is the difference for you (if any) between disability and dis Ability?
One of the most interesting, and rapid, recent changes in live stand-up comedy is the increased number of disabled comedians performing. This chapter examines the performances of two disabled comedians – Laurence Clark and Rosie Jones – to explore how their performances may be viewed as social justice comedy through an analysis of the techniques used, and themes explored, in their performances. The chapter begins by considering the ways in which disability has been represented in comedy across history. Attention then shifts to how stand-up comedy can be considered a tool for social justice. The focus then turns to the methodological framework used to gather and analyse performances by Laurence Clark and Rosie Jones, before examining how the techniques used, and themes explored, in their performances may have social justice potentials and impacts for disability and disabled people and how the limits to these potentials and impacts can be understood.
The city of Indore in Madhya Pradesh, India, is home to over 1 million individuals with disabilities. Despite this significant population, the public schools serving these communities often lack visibility and a dependable online presence. Information about these institutions is usually dispersed through unreliable channels, leaving the pedagogies and amenities primarily misunderstood. This article discusses the ideation, development, and completion of a public humanities initiative, “‘Only Connect!’ Empowering Public Schools for the Disabled in Indore to engage in a participatory and inclusive online public sphere,” a U.S. Alumni micro-grants project initiated and finalized in 2022. Only Connect! is a pioneering online platform that offers verified contact details for all public schools in Indore, catering to children who are Deaf, Blind, and those who suffer from speech difficulties between the ages of 6 and 18. The project’s central mission is to dispel the myths and inaccuracies surrounding disability education. Based on the narratives sourced from comprehensive fieldwork, surveys, and extensive interviews with key stakeholders, including school principals and parents, Only Connect! aims to foster a better-informed and supportive community. The goal of this project is to facilitate dialogue about the challenges and opportunities in educating disabled students in Indore, promoting greater understanding and inclusivity.
This chapter explores how the term ‘Chernobyl child’ expanded over time to encompass nearly all children from Belarus and Ukraine, categorized based on their perceived suffering and need for help. This classification, while useful for securing aid, often led to ethical dilemmas about who deserved assistance. Through specific examples, the chapter illustrates how this categorization not only shaped their experiences abroad but also influenced how they and others understood their identities. The chapter also delves into how these trips abroad served as a means for the children to cope with the trauma of the Chernobyl disaster. While these journeys opened their eyes to different cultures, they often involved significant emotional challenges, such as adjusting to unfamiliar environments and confronting the reality of their situation. These experiences, though difficult, played a crucial role in how the children processed their pasts and envisioned their futures. The chapter shows that, despite the challenges, the trips sometimes led to lasting relationships with host families, providing a complex blend of support and difficulty in dealing with their traumatic histories.
Chapter 2 explores an important premise which underlies this critique of the law: it examines the idea that disfigurement inequality is a problem which merits a legal response – namely the granting of protective rights under the Act. It concludes that, despite some uncomfortable distinctions, there is a compelling case for a legal response in this area. The nature of law’s current response is then laid out. Relevant parts of the international legal framework – including EU law, the UN Convention on the Rights of Persons with Disabilities (‘CRPD’) and decisions of the European Court of Human Rights (‘ECtHR’) applying the European Convention on Human Rights – are explained by reference to the models of disability which implicitly inform them.
The so-called Holiness Code of Leviticus highlights the importance of ethical living if Israel is to be holy as God is holy. This chapter discusses the historical-critical arguments around the composition of the Holiness Code but focuses mainly on bridge Leviticus creates between the holiness of Israel’s tent and God’s tent. Ethical purity is as important as ritual purity in Leviticus and requires holiness in every aspect of Israel’s life.
The previous chapters have explored the teaching methodologies and concepts related to different forms of the Arts, as well as methodologies for integration and organisation. However, in addition to being able to teach the Arts, we need to have in place a system for evaluating the teaching process to ensure the outcomes and goals we wish to achieve are met for the learners. There has been a great deal of research to identify specific teaching practices that can improve children’s outcomes. This chapter does not intend to analyse the validity or otherwise of these outcomes, as these are mandated by the various examination and education boards. In part, this is because it is difficult to isolate any specific technique or learning skill that works for individuals because all children have unique and individual learning styles. For these reasons, the focus of recent research has been to isolate general characteristics. This chapter looks at the application of reflective learning tools to enhance teaching of the Arts, as well as inclusion and diversity in the classroom (specifically disability). Its focus, therefore, is to separate teaching from subjective assessment of teachers.
Functional impairment in daily activities, such as work and socializing, is part of the diagnostic criteria for major depressive disorder and most anxiety disorders. Despite evidence that symptom severity and functional impairment are partially distinct, functional impairment is often overlooked. To assess whether functional impairment captures diagnostically relevant genetic liability beyond that of symptoms, we aimed to estimate the heritability of, and genetic correlations between, key measures of current depression symptoms, anxiety symptoms, and functional impairment.
Methods
In 17,130 individuals with lifetime depression or anxiety from the Genetic Links to Anxiety and Depression (GLAD) Study, we analyzed total scores from the Patient Health Questionnaire-9 (depression symptoms), Generalized Anxiety Disorder-7 (anxiety symptoms), and Work and Social Adjustment Scale (functional impairment). Genome-wide association analyses were performed with REGENIE. Heritability was estimated using GCTA-GREML and genetic correlations with bivariate-GREML.
Results
The phenotypic correlations were moderate across the three measures (Pearson’s r = 0.50–0.69). All three scales were found to be under low but significant genetic influence (single-nucleotide polymorphism-based heritability [h2SNP] = 0.11–0.19) with high genetic correlations between them (rg = 0.79–0.87).
Conclusions
Among individuals with lifetime depression or anxiety from the GLAD Study, the genetic variants that underlie symptom severity largely overlap with those influencing functional impairment. This suggests that self-reported functional impairment, while clinically relevant for diagnosis and treatment outcomes, does not reflect substantial additional genetic liability beyond that captured by symptom-based measures of depression or anxiety.
This article is concerned with the history of eugenic sterilisation in Britain through the 1920s and 1930s. In this period, the Eugenics Society mounted an active but ultimately unsuccessful campaign to legalise the voluntary surgical sterilisation of various categories of people, including those deemed ‘mentally deficient’ or ‘defective’. We take as our explicit focus the propaganda produced and disseminated by the Eugenics Society as part of this campaign, and especially the various kinds of data mobilised therein. The parliamentary defeat of the Society’s Sterilisation Bill in July 1931 marks, we argue, a significant shift in the tactics of the campaign. Before this, the Eugenics Society framed sterilisation as a promising method for eradicating, or at least significantly reducing the incidence of, inherited ‘mental defect’. Subsequently, they came to emphasise the inequality of access to sterilisation between rich and poor, (re)positioning theirs as an egalitarian campaign aimed at extending a form of reproductive agency to the disadvantaged. These distinct phases of the campaign were each supported by different kinds of propaganda material, which in turn centred on very different types of data. As the campaign evolved, the numbers and quantitative rhetoric which typified earlier propaganda materials gave way to a more qualitative approach, which notably included the selective incorporation of the voices of people living with hereditary ‘defects’. In addition to exposing a rupture in the Eugenics Society’s propagandistic data practices, this episode underscores the need to further incorporate disabled dialogues and perspectives into our histories of eugenics.
The plays of Sean O’Casey are filled with aches and pains, debilitating diseases, and traumatic wounds. He was himself a disabled writer. Furthermore, his presentation of disease and disability is inseparable from his critique of class, militarism, and masculinist ideology. This chapter shows how O’Casey’s depictions of disability are more nuanced than they may at first appear. He does demonstrate an essentialist tendency to see female resilience as a triumph over the failures of male impairment, yet, in plays such as Juno and the Paycock and The Silver Tassie, O’Casey allows space for contrary readings that speak with relevance to contemporary understandings of disability.
This chapter replays the origin story of whiteness to better recover how Toni Morrison, in her field-defining Playing in the Dark (1992), identified whiteness’s hauntings by the twinned shadow of Blackness and disability. By rereading Morrison’s interpretation of Edgar Allan Poe’s 1838 The Narrative of Arthur Gordon Pym, the chapter traces out how the critical study of whiteness needs to reevaluate and expand key ableist concepts and terms within the field lest it repeat and reinscribe disability oppression. Returning to Morrison’s foundational essay identifies interpretive strategies for a “crip abolitionist critique” that dismantles an entangled history of whiteness and disability. In its last section, the chapter then maps out this crip abolitionist methodology for whiteness studies through a reading of Victor LaValle’s 2012 novel The Devil in Silver, in which LaValle reimagines the white race traitor as an abolitionist caretaker.
This study presents the most recent data on the incidence, prevalence, and years lived with disability (YLDs) due to anxiety disorders across the Middle East and North Africa (MENA) region from 1990–2021, analysed by sex, age, and sociodemographic index (SDI).
Methods:
We reported the burden of anxiety disorders using data sourced from the Global Burden of Disease 2021 study. The estimates of prevalence, DALYs, and YLDs are provided as numbers and age-standardised rates, accompanied by their 95% uncertainty intervals (UIs).
Results:
In 2021, the age-standardised point prevalence of anxiety disorders in the region was 5.95 thousand, with an incidence rate of 883.4 per 100,000. The number of YLDs in 2021 reached 4.5 million. From 1990 to 2021, the burden of anxiety disorders increased significantly. Lebanon had the highest burden in 2021. Among both sexes, the 10–14 age group had the highest incidence rate, while the 15–19 age group had the highest prevalence and YLD rates. In 2021, most age groups in the MENA region had YLD rates that were higher than the global average.
Conclusion:
This study highlights the urgent need for a multidisciplinary approach to prevent and manage anxiety disorders. Ensuring accessible and affordable treatment options for all affected individuals is crucial. Governments should prioritise supporting programmes to effectively address mental health issues, given the unique socioeconomic and geopolitical challenges in the MENA region. By including effective preventive methods alongside treatment in healthcare strategies, the burden of anxiety disorders can be significantly reduced.
Disability is a common and universal human experience. Yet, people with disabilities (PWDs) are in poorer health and have less access to quality healthcare than their non-disabled peers. In fact, the National Institutes of Health’s (NIH) designated PWDs as a health disparities population in 2023. This paper illustrates the application of translational science (TS) principles to overcoming roadblocks to reducing PWDs’ health disparities. Part I provides an overview of health disparities among PWDs and the recent designation – situating both within a TS framework. Part II summarizes literature on specific factors that contribute to PWDs’ exclusion from research, how these factors are reflected in background reports that impelled the designation of PWDs as a disparity population, and how the suggested steps to implement the designation reflect TS principles and its research agenda. Part III describes “Reducing Researcher Roadblocks to Including People with Disabilities in Research (D2/R3),” a TS solution to overcoming PWDs exclusion from research. D2/R3 is our institution’s Clinical and Translational Science Award research project – a mixed-methods study that targets research teams’ knowledge, attitudes, biases, and perceptions that contribution to under representation of persons with developmental disabilities in research.