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Presented as a ‘formal metacomic’ (Cook RT, 2017, Metacomics. In Bramlett F, Cook RT and Meskin A (eds), The Routledge Companion to Comics. New York, NY: Routledge, pp. 257–266. https://doi.org/10.4324/9781315851334-32) and understood through Gillian Whitlock’s ‘autographic’ (Whitlock G, 2006, Autographics: The seeing “i” of the comics. Modern Fiction Studies52(4), 966. https://doi.org/10.1353/mfs.2007.0013), this article explores techniques such as abstraction and multiple narrative threads in autobiographical comics, highlighting their storytelling potential from a neurodivergent, ADHD perspective. It aims to advance comic creation as a research and sharing tool for diverse experiences, viewing autographics as a form of critical literacy through which art and activism intersect. The work emphasizes neurodivergent activism through the metaphor of abstraction, which both resists and invites narrative through sequencing. This aligns with the work of J Baetens (2011, Abstraction in comics. SubStance40(1), 94–113. https://doi.org/10.1353/sub.2011.0004), who describes abstraction as anti-narrative. In this concept, a tension exists, since sequencing superimposes narrative onto abstract images, revealing multiple truths. This aligns with neurodivergent experiences, where various ways of perceiving co-exist. The work positions comics as a form of academic resistance and autoethnographic activism.
Autism is marked by substantial heterogeneity in cognitive, affective, behavioral, and neural profiles. This heterogeneity among diagnosed individuals is also reflected in the broad spread of autistic traits in the general population. Moving beyond a narrow focus on social-communication and/or repetitive-behavior differences, contemporary accounts increasingly emphasize multidimensional and transdiagnostic processes and the need to integrate evidence across levels of analysis, from self-report and cognitive measures to neuroimaging and computational models. The contributions in this Special Issue collectively advance this agenda by providing insights into individual differences in autistic traits and autism-relevant phenotypes, clarifying their measurement and stability, and proposing mechanistic frameworks that can help explain why diverse profiles emerge. In this conclusion piece, we summarize the manuscripts included in the special issue, highlight shared themes and discuss remaining issues and future directions, particularly related to naturalistic, interactive neuroscience. Ultimately, we hope this work will contribute to the development of more precise and inclusive models of autism.
CBT training programmes increasingly emphasise widening participation and workforce sustainability; however, limited research has explored how neurodivergent trainees and practitioners experience the academic and pedagogical structures through which CBT competence is developed and assessed. This study examined how neurodivergence, specifically the author’s dyslexia and dyspraxia, shaped engagement with CBT training, academic assessment, and pedagogical leadership, and considered implications for inclusive and authentic competence development. A critical autoethnographic approach was employed, drawing on reflective narratives situated within neurodiversity theory, experiential learning models, and Universal Design for Learning (UDL) frameworks. Four interconnected themes emerged: (1) academic norms functioning as structural barriers to competence demonstration; (2) the hidden emotional and cognitive labour of navigating academic systems; (3) neurodivergent strengths within experiential learning and clinical formulation; and (4) transformation of lived experience into inclusive pedagogical redesign within CBT training programmes. The barriers described here reflect systemic misalignment between traditional academic structures and experiential competence development rather than individual deficit; while grounded in dyslexic and dyspraxic experience, they may resonate across neurodivergence. UDL-informed curriculum design and diversified assessment approaches may enhance accessibility, authenticity of competence evaluation, and workforce sustainability within CBT education.
Key learning aims
(1) To understand how neurodivergent identity shapes experiences of CBT training and academic engagement.
(2) To recognise systemic academic barriers affecting neurodivergent CBT trainees and practitioners.
(3) To explore the role of experiential learning and inclusive pedagogy in supporting diverse learners.
(4) To identify implications for assessment design and curriculum development within CBT training programmes.
This paper argues for three main claims: (i) belonging can play an important role for epistemic self-trust; (ii) epistemic self-trust can be construed plurally so as to include not only its intellectual or propositional dimensions but also its experiential (practical, tacit, embodied, and affective) dimensions; and (iii) self-trust, plurally construed, can serve as a mechanism of epistemic repair to counteract various forms of epistemic injustice that undermine epistemic agency along these propositional and experiential dimensions. To make this threefold argument, I turn to the context of neurodiversity and neuronormativity, which helpfully illustrates the plural dimensions of epistemic agency, epistemic self-trust, and epistemic repair.
To explore existing knowledge on autism in medical education and early clinical training, examine the lived experiences of autistic doctors, review relevant National Health Service policies and legal frameworks, and propose a practical framework for improving inclusion. This study comprised a narrative review of the published literature on autism in medical education, foundation training and healthcare settings, supplemented by a positionality statement informed by the author’s clinical experience.
Results
Common barriers include the hidden curriculum of clinical placements, neurotypical templates in communication assessment, sensory demands of clinical environments, significant risks associated with disclosure and inadequate supervisor awareness. Masking imposes substantial psychological costs, including risk of autistic burnout. Legal frameworks exist but are inconsistently applied in practice. The SUPPORT framework is proposed as a structured model: Structured learning environments, Understanding neurodiversity, Predictability, Practical adjustments, Open culture, Relationships and mentorship, and Trainee well-being.
Clinical implications
Autistic doctors bring valuable strengths to clinical practice. The barriers they face during the transition from medical school to clinical practice are documented and preventable. Despite legal protections and growing awareness of neurodiversity, National Health Service training frameworks do not consistently address the needs of autistic clinicians. The SUPPORT framework provides a practical, low-resource approach to addressing these barriers, with implementation requiring greater awareness and institutional commitment. These findings identify the need for medical training to move past recognition of neurodiversity and towards creating clinical environments in which autistic doctors can thrive.
Since the 1940s, the concept of autism has undergone marked changes, and autism spectrum disorder (ASD) is a wildly heterogenous condition. At the same time, the prevalence of ASD has increased massively.
Methods
This essay considers possible reasons for the changes and their consequences.
Results
Among drivers for the increase in prevalence are cultural changes, such as the desire for inclusion, harm avoidance, reliance on self-report, and the acceptance of masking. These have all led to a lowering of the diagnostic threshold. Furthermore, the popularity of the concept of autism boosted numbers via self-diagnosis and a search for identity.
Conclusions
Marked differences now exist between those first diagnosed in childhood and others first diagnosed in adolescence or adulthood. The time has come to examine reasons for these conceptual changes and the consequences for clinical practice and research.
In this chapter, we examine the experiences of neurodivergent autistic people and attention deficit hyperactivity disorder (ADHD) individuals around menstruation and the life transition of menopause. The chapter is informed by personal insights from neurodivergent individuals with first-hand encounters of menstrual and menopausal challenges, our ‘experts by experience’. In doing so, we aim to inform and empower clinicians to appropriately support these patients with their menstrual and menopausal health. We begin by discussing what autism and ADHD are, the features of these conditions, and why they are particularly relevant and important in regard to health needs and for healthcare, and the shared interpersonal-environmental and intrapersonal factors of autistic people and ADHD individuals (ADHDers). We then individually consider autistic and ADHD experiences of menstruation and menopause with narrative from our experts by experience. Based on this information, we provide point-by-point advice for health professionals supporting neurodivergent people with menstruation and menopause health.
Divergent and convergent thinking are critical processes in design, ensuring that solutions are plentiful, widely applicable, original and useful. Prior research has examined the cognitive underpinnings of these types of thinking, including the relationship between cognitive load and task performance. Additionally, prior research has highlighted the impact of ADHD on divergent and convergent thinking performance and the impact of ADHD on eye-tracking metrics. However, limited research has studied the impact of ADHD on eye-tracking metrics during convergent and divergent thinking tasks, particularly in a design context. In this exploratory study with undergraduate engineering students, we aim to compare saccades, fixations and pupil diameter – proxies for cognitive load – between participants with and without ADHD performing convergent and divergent thinking design tasks. We find no significant differences between individuals with and without ADHD; however, participants, irrespective of ADHD diagnosis, exhibited more frequent saccades, shorter fixations, smaller ranges in pupil diameter and larger standard deviations in pupil diameter during the convergent thinking task. We discuss the possible implications of these differences on our understanding of creativity using eye-tracking metrics.
Edited by
Liz McDonald, East London NHS Foundation Trust,Roch Cantwell, Perinatal Mental Health Service and West of Scotland Mother & Baby Unit,Ian Jones, Cardiff University
Autism research and clinical practice is a rapidly evolving branch of psychiatry. This chapter explores autism through the lenses of the neurodiversity paradigm, challenging the deficit-based model whilst remaining stark about significant healthcare inequalities and challenges that autistic people face. It considers the perinatal journey from an autistic perspective, highlighting some of the common challenges autistic mums (to be) can face, and makes suggestions for approaches to take when working with autistic patients.
This chapter examines the various definitions and models used to conceptualise and diagnose dyslexia. The authors critique traditional approaches such as the discrepancy model and response to intervention (RTI), arguing that these methods are inadequate – particularly for adolescents and adults. Instead, they advocate for the profile of strengths and weaknesses (PSW) model, which accounts for underlying cognitive inefficiencies, such as working-memory deficits, to explain functional impairments in skills such as reading and writing. The chapter also explores the biological and neurological foundations of dyslexia, including genetic influences and structural brain differences, and challenges simplistic or euphemistic views such as ’neurodiversity’ that may obscure understanding. Emphasising a scientific, empirical lens, the authors reject models based purely on social narratives or lived experiences, advocating instead for the biopsychosocial model that integrates biological, psychological, and environmental factors. Dyslexia is positioned not merely as a reading issue but as a complex cognitive disorder with broad implications across the lifespan. The chapter closes by asserting the need for clear, evidence-based conceptual models to foster self-understanding, improve assessment, and guide effective intervention.
This chapter characterises the beginning of the 1810s as a transitional moment for both early feminist thought and cultural conceptions of intellectual disability. Through a sustained reading of Lucy Aikin’s critically underexamined Epistles on Women (1810), the chapter argues that the long, combative poem articulates an intersectional appeal to feminine-coded weakness, idiocy, and disability. The opening question of the poem, ‘when was ever weakness in the right?’, pits a utopian matriarchal future against the overwhelming misogyny and brutality of the masculinist past. Aikin’s revisionist history begins in Eden with Eve’s assiduous care for the ‘moping idiot’ Adam and ends in the modern era with the new ideal of feminine friendship supplanting compulsory ideologies of heteropatriarchal marriage. Throughout, Aikin creatively develops a compelling feminist aesthetics and ethics grounded in the complex trope of idiocy and neurodiversity.
The Epilogue provides a reflective distillation of the book’s major claims and anticipatory warnings. It revisits the central idea that the human species is entering a new epoch of cognitive modulation — one that combines the ancient allure of psychoactive substances with the unprecedented reach of digital simulation. It affirms that while such tools offer extraordinary opportunities for creativity, healing, and connection, they also pose significant risks to autonomy, mental integrity, and collective meaning-making. The epilogue emphasises the urgency of ethical design, regulatory foresight, and public education to manage this dual-edged transformation. It concludes with a speculative yet grounded vision: that the next phase of human evolution may depend less on biology and more on how we symbolically navigate our internal and external realities. The final call is for conscious engagement — with our histories, technologies, and altered states — to ensure our adaptations remain humane and meaningful.
This integrative chapter highlights the interdisciplinary implications of the book’s core arguments. It synthesises the historical, neuroscientific, cultural, and ethical perspectives covered in earlier chapters, showing how they converge around a central theme: the human impulse to reshape consciousness through external means. The summary identifies key throughlines such as the neurochemical basis of thrill-seeking, the symbolic encoding of drug use, the commodification of altered states, and the rise of digital simulation as a new frontier of mind alteration. It stresses the importance of cross-disciplinary collaboration in addressing emerging challenges — including addiction, mental health, identity fragmentation, and regulatory vacuums. The chapter proposes that future research and policy must account for the hybrid nature of cognitive environments, shaped by both chemical inputs and algorithmic systems. Ultimately, it reaffirms the need to develop new cultural literacies and ethical frameworks suited to the complexities of the digital-chemical age.
School refusal among neurodivergent students underscores systemic failures in traditional educational systems. This qualitative study, informed by the neurodiversity paradigm, examines how Flexible Learning Options (FLOs) in South Australia address drivers of disengagement, such as sensory overload, punitive discipline, and identity erasure, while fostering reengagement through autonomy, relational safety, and identity empowerment. Drawing on interviews conducted with a subsample of 18 students aged 13–19, reflexive thematic analysis resulted in the development of three themes: (1) autonomy and its limits, (2) relational safety as harm reduction, and (3) identity empowerment through neuroaffirmation. The findings reported in this paper advocate for educational models that transform flexibility from a temporary solution into a blueprint for equity, ensuring schools become spaces of support rather than harm for neurodivergent learners.
In his target article, ‘Autism, constructionism, and nativism’, Kissine (2021) argues that data from autism should be taken into consideration in the debate about L1 acquisition. This paper responds to Kissine's piece by pointing out several of its underlying assumptions and suggesting directions for future research on the topic. Traditional framings of autism as a deficit have recently been challenged in favor of an identity-based approach, the neurodiversity paradigm, which suggests that autistic speech should not be measured in terms of its resemblance to nonautistic speech and that literature on intercultural miscommunication may offer insights into autistic communication. There are some indications that distinct autistic discourse practices may be identifiable in communities of practice, and studies on autistic literacy could benefit from considering the theoretical perspectives found in literature on multimodality and translanguaging. Finally, research on language acquisition might be strengthened by the incorporation of holistic neurocognitive theories about autistic minds.
Autistic adolescents are at higher risk of self-harm, suicidal behaviours, and emotion dysregulation compared with their non-autistic peers. Dialectical behaviour therapy (DBT) is an evidence-based treatment for self-harm and suicidal behaviour with emerging literature of the application of DBT for autistic populations. Despite this, no qualitative research has investigated the experiences of autistic adolescents of standard DBT. Therefore, this study aimed to explore autistic adolescents’ experiences of non-adapted DBT. Ten adolescents who had or were seeking an autism diagnosis, and were in a DBT programme, completed semi-structured interviews. Qualitative data from the interviews were analysed using reflexive thematic analysis. Themes were generated for each objective. Objective 1 included themes about the lived experience of autistic adolescents accessing DBT, including: ‘The impact of invalidation’, ‘Fostering acceptance and understanding’, ‘What does autism mean to me?’, and ‘Autism and mental health difficulties’. The themes regarding Objective 2 were about the experiences of the various modes of DBT and were organised by each client-facing mode. Objective 3 included themes highlighting the experience of utilising DBT skills in daily life, which included: ‘Barriers to skills use’, ‘Supporting skills use’, and ‘Skills practice or masking?’. Finally, Objective 4 included themes regarding the recommendations participants had for optimising DBT for autistic people: ‘Improving written materials’ and ‘General accessibility advice’. These findings suggest for DBT therapists to embody cultural humility, curiosity, validation, and flexibility when building neuro-affirmative competencies for supporting autistic individuals. Results are discussed in relation to the application and acceptability of DBT for this group.
Key learning aims
(1) Recent publications (e.g. Keenan et al., 2023) have explored the experience of autistic adults accessing DBT and highlighted the need for clinicians to work collaboratively with clients and make reasonable adjustments to improve autistic adults’ understanding and adherence to DBT.
(2) To date, no qualitative studies have explored the experience of autistic adolescents accessing the Rathus and Miller (2015) Adolescent DBT model. The current study explores the views of autistic adolescents on how autism is discussed and considered by clinicians when supporting them to access different components of DBT when describing the strengths and barriers they experience.
(3) Adopting a bottom-up approach, we identify key themes from adolescents’ perspectives on how to support them to access and engage with different DBT components, ranging from making environmental adaptations to meet individual sensory needs to improve accessibility, to providing more opportunities for personalised learning using neuro-affirmative examples that can improve generalisability of skills in everyday life. We provide recommendations for clinicians to consider on ways of adapting the process and content of DBT to increase accessibility and engagement for autistic adolescents in treatment.
We humans are diverse. But how to understand human diversity in the case of cognitive diversity? This Element discusses how to properly investigate human behavioural and cognitive diversity, how to scientifically represent, and how to explain cognitive diversity. Since there are various methodological approaches and explanatory agendas across the cognitive and behavioural sciences, which can be more or less useful for understanding human diversity, a critical analysis is needed. And as the controversial study of sex and gender differences in cognition illustrates, the scientific representations and explanations put forward matter to society and impact public policy, including policies on mental health. But how to square the vision of human cognitive diversity with the assumption that we all share one human nature? Is cognitive diversity something to be positively valued? The author engages with these questions in connection with the issues of neurodiversity, cognitive disability, and essentialist construals of human nature.
This chapter focuses on the second bridge between economic and social values in contract law, examining the role played by regulation in bringing together these values. The discussion questions the effectiveness of regulatory responses to business to consumer (B2C) relations in English consumer contract law, in protecting people not just as economic actors, but also as citizens, and in safeguarding values such as autonomy and human dignity. The analysis focuses on the regulation of unfair contract terms, unfair commercial practices, implied terms in contracts for the provision of goods, services and digital content, and on information and cancellation rights in business to consumer (B2C) contracts. This chapter also examines the concept of consumer vulnerability in trader– consumer relations.
Mirroring the general population, the number of medical students, doctors and, indeed, psychiatrists disclosing being neurodivergent is rising. These individuals commonly have a variety of strengths that can enhance their work, but these strengths may go unrecognised. All too often such individuals have been labelled ‘doctors in difficulty’. We begin this article with a review of contemporary thinking regarding neurodiversity, before considering specific issues facing neurodivergent doctors, specifically psychiatrists. We explore neurodivergent strengths and the evidence regarding career outcomes and mental health. We discuss the stigma that many neurodivergent psychiatrists face in the medical sphere and how difficulties may be reframed as unmet needs. We highlight initiatives that aim to change workplace culture, before discussing the concept of reasonable adjustments, alongside a wide range of practical suggestions of adjustments to consider, using the Autistic SPACE framework and the Royal College of Psychiatrists’ reasonable adjustments guidance. Finally, we consider how those in senior leadership roles can contribute to this field and provide role modelling and signposting to further information and support for neurodivergent doctors and their supervisors and line managers.
This chapter focuses on the influence of nineteenth-century neurology on Beckett’s writing, especially the work of Jean-Martin Charcot and Georges Gilles de la Tourette, who both worked at the Salpêtrière Hospital in Paris. Charcot’s famous Tuesday lectures, at which he exhibited his patients to admiring crowds, became an intellectual and middle-class pastime in Paris, instigating a new performance style in the Parisian café-concert, in cabaret, and in music hall, while the performers at such venues, in turn, became the stars of early cinema, adapting their convulsive performance style to silent film. Beckett took a lifelong interest in these popular forms, and the chapter considers the impact of their convulsive aesthetic on his work. It also addresses Beckett’s representation of speech and his reading of Bergson’s 1900 essay on Laughter, which argued that humour arises from ‘something mechanical encrusted on the living’. Bergson’s extended essay was itself substantially influenced by medical discoveries, and especially the theatrical and often spectacular culture of the late-nineteenth-century science of neurology. While Beckett diverges from Bergson’s Cartesian stance, he nevertheless concurred on the limitations of free will and agency, on ‘the deep-seated recalcitrance of matter’, and on the human as always already determined by the mechanical.