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The Anverse of Mirror

Another History of Madness Narrated by the Persons

Discover how the voices of those labeled mad have been systematically silenced, reinterpreted, and erased from psychiatric history—and how centering patient narratives fundamentally transforms our understanding of mental illness.

238 pages12 chaptersJan 15, 2026PsychiatryCreated by Alvaro

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About this book

This book examines psychiatric history not through the lens of medical authority, but through the lived experiences, resistance, and agency of patients themselves. You'll explore how narrative bioethics and personalistic care frameworks offer ethical alternatives to traditional psychiatry, analyze the social construction of madness across historical periods, and understand how deinstitutionalization movements and neurodiversity frameworks challenge psychiatric epistemology. Through asylum memoirs, archival analysis, and first-person accounts, you'll examine the power dynamics that shaped institutional psychiatry, the resistance strategies employed by those confined, and the recovery narratives that reclaim agency. This book equips you with critical tools for analyzing psychiatric literature, understanding the genealogy of madness as a concept, and recognizing how cultural attitudes, classification systems, and institutional practices have continuously redefined what it means to be mad. Essential reading for students seeking to understand psychiatry's hidden histories and imagine more ethical futures.

Table of contents

  1. IntroductionWhy Patient Voices Matter: The Silenced History of Psychiatry, The Narrative Turn: From Medical Records to First-Person Accounts, How This Book Is Organized: A Guide to Reading the AnverseRead below
  2. Chapter 1: Genealogies of Madness: Tracing the Historical Construction of Mental IllnessMadness Before Psychiatry: Pre-Modern Understandings and Spiritual Frameworks, The Birth of Psychiatric Authority: How Madness Became a Medical Problem, The Evolution of Madness Symptoms: How Diagnostic Categories Changed Over Time
  3. Chapter 2: Psychiatric Epistemology: What We Think We Know About MadnessFoundations of Psychiatric Knowledge: How Psychiatry Claims Authority, Classification Systems Under Scrutiny: Critiquing Diagnostic Categories, Alternative Ways of Knowing: Phenomenology, Neurodiversity, and Beyond
  4. Chapter 3: Institutional Power and the Asylum: Architecture of ControlDesigning Madness: How Asylum Architecture Enforced Authority, Surveillance and Control: Power Dynamics Within Institutional Walls, The Erasure of Patient Voice: How Records Silenced Those They Documented
  5. Chapter 4: Reading Asylum Memoirs: Patient Narratives as Historical EvidenceAnalyzing Asylum Memoirs: Methods for Reading Patient Narratives, Narratives of Resistance: How Patients Contested Medical Authority, Finding Patient Voice in Archives: Recovering Hidden Testimonies
  6. Chapter 5: The Phenomenology of Madness: Lived Experience Beyond DiagnosisThe Subjective World: Understanding Madness From the Inside, Embodied Madness: How the Body Experiences and Expresses Divergence, Making Meaning: How Individuals Interpret Their Own Experiences
  7. Chapter 6: Social Construction of Mental Illness: Culture, Power, and PathologyCultural Attitudes Toward Madness: How Societies Define Deviance, Power and Pathology: Who Decides What Is Normal?, Historical Variation: How Madness Means Different Things in Different Times
  8. Chapter 7: Anti-Psychiatry and Resistance Movements: Challenging Medical AuthorityOrigins of Anti-Psychiatry: Intellectual and Activist Critiques, Resistance Within Asylums: Patient Activism and Collective Action, Contemporary Resistance: Mad Pride and Neurodiversity Movements
  9. Chapter 8: Deinstitutionalization: History, Promise, and FailureThe Deinstitutionalization Movement: Origins and Ideals, Implementation and Reality: What Happened When Asylums Closed, Lessons Learned: Rethinking Community Mental Health
  10. Chapter 9: Neurodiversity and Mad-Studies: Reframing Mental DivergenceThe Neurodiversity Framework: Beyond Deficit Models, Mad-Studies Philosophy: A Revival of Critical Perspectives, Disability Rights in Psychiatry: Centering Disabled Voices
  11. Chapter 10: Narrative Bioethics: Ethical Frameworks for Personalistic CareFoundations of Bioethics in Mental Health: Principles and Critiques, Narrative Bioethics: Centering Stories and Lived Experience, Personalistic Care Approaches: Honoring Dignity and Agency
  12. Chapter 11: Recovery Narratives and Agency: Reclaiming Voice and PowerWhat Is Recovery? Beyond Medical Cure to Personal Meaning, Narratives of Agency: How Individuals Navigate and Transcend Diagnosis, Patient-Centered Research Methods: Ethical Approaches to Studying Madness
  13. Chapter 12: Psychiatric Literature and Representation: How Madness Is PortrayedLiterary Narratives of Madness: Fiction, Memoir, and Testimony, Stigma in Mental Health Discourse: Language, Representation, and Power, Narrative Analysis Methods: Tools for Reading Psychiatric Texts
  14. ConclusionSynthesis: Toward an Ethics of Listening, Future Directions: Imagining More Ethical Psychiatries
  15. Further Reading and Resources

Introduction

Psychiatric history has traditionally been written by those who held the keys—the physicians, administrators, and reformers who designed asylums, classified symptoms, and determined treatments. Their voices dominate the archives, textbooks, and historical accounts that shape how we understand mental illness today. Yet this official history obscures a fundamental truth: those labeled mad possessed their own perspectives, experiences, and interpretations of what was happening to them. Their narratives, when they survive at all, reveal a profoundly different story—one in which psychiatric authority was contested, diagnostic categories were experienced as violence, and institutional care often meant systematic erasure of personhood. This book invites you to examine psychiatric history through what we call the anverse of the mirror—the reflection that shows what institutional psychiatry has consistently failed to see or deliberately ignored.

The concept of the anverse draws from the idea that every mirror has two sides: the reflective surface that shows what we expect to see, and the backing that makes reflection possible but remains hidden from view. Traditional psychiatric history presents the reflective surface—the progress narrative of medical science conquering irrationality, the humanitarian reforms that replaced chains with treatment, the diagnostic manuals that brought order to chaos. But the anverse reveals the structures that made this reflection possible: the power relations that determined whose voice counted as knowledge, the institutional practices that transformed human suffering into medical objects, and the resistance strategies through which patients asserted their humanity against systems designed to deny it. Understanding psychiatric history requires examining both surfaces simultaneously, recognizing that what appears as scientific progress from one angle may look like systematic oppression from another.

This introduction establishes why centering patient narratives fundamentally transforms our understanding of psychiatric history and practice. You'll discover how the narrative turn in medical humanities has created new methodologies for recovering silenced voices, why first-person accounts challenge psychiatric epistemology in ways that clinical research cannot, and how this book is organized to guide you through increasingly complex engagements with patient perspectives. The goal is not to replace medical knowledge with patient testimony, but to develop what we call critical bifocal vision—the ability to hold both perspectives simultaneously, understanding how they illuminate and challenge each other. This approach is essential for anyone seeking to practice mental health care ethically, conduct research that honors human dignity, or understand how psychiatric systems have shaped and continue to shape human lives.

Why Patient Voices Matter: The Silenced History of Psychiatry

The systematic silencing of patient voices in psychiatric history was not accidental but structural, built into the very foundations of institutional psychiatry. When Philippe Pinel famously liberated the insane from their chains at the Bicêtre Hospital in 1793, he simultaneously established a new form of control: medical authority over the interpretation of madness. Patients could speak, but their words were reframed as symptoms rather than testimony. A patient's protest against confinement became evidence of lack of insight; their alternative explanations for their experiences were documented as delusions; their resistance to treatment proved the severity of their illness. This interpretive framework created what historian Roy Porter called a dialogue of the deaf—patients spoke, physicians recorded, but genuine communication across the power divide rarely occurred[1]. The archive of psychiatric history is thus filled with patient words that have been systematically stripped of their intended meanings.

Consider the case of Elizabeth Packard, confined to the Jacksonville Insane Asylum in Illinois in 1860 by her husband for the insanity of disagreeing with his Calvinist theology. Packard's extensive writings from the asylum reveal a woman of remarkable clarity, documenting the arbitrary nature of her confinement and the institutional practices that punished independence of thought. Yet her medical records describe her as suffering from monomania characterized by religious delusions and inappropriate assertiveness for a married woman. The same behaviors—writing, reasoning, arguing theological points—that would have been unremarkable in a man were reinterpreted as symptoms when performed by a woman challenging her husband's authority. Packard eventually secured her release and became a prominent activist for married women's rights and asylum reform, publishing multiple books that exposed the legal mechanisms allowing husbands to institutionalize wives without due process[2]. Her case illustrates how psychiatric diagnosis has historically functioned as a tool for enforcing social conformity, particularly regarding gender, race, class, and political dissent.

The silencing of patient voices operated through multiple mechanisms that you must understand to recognize their ongoing effects:

  • Epistemic invalidation: Patient testimony was categorically dismissed as unreliable due to their mental state, creating a circular logic where being diagnosed meant losing credibility to contest the diagnosis
  • Linguistic reinterpretation: Patient statements were translated into medical terminology that stripped away their social and political content, transforming complaints about institutional conditions into symptoms of illness
  • Archival erasure: Patient writings were often destroyed, confiscated, or never preserved in institutional archives, while physician notes and administrative records were carefully maintained
  • Legal disenfranchisement: Commitment laws removed patients' legal standing to testify, sign contracts, or advocate for themselves, making their voices literally inadmissible in legal proceedings
  • Physical isolation: Asylum architecture and regulations prevented patients from communicating with the outside world, limiting their ability to share their experiences with anyone who might advocate for them
  • Therapeutic justification: Silencing was reframed as treatment, with physicians arguing that allowing patients to express their delusions would reinforce pathological thinking
These mechanisms worked synergistically to create what philosopher Miranda Fricker calls epistemic injustice—the systematic exclusion of certain groups from participation in knowledge production[3].

The consequences of this silencing extend far beyond historical interest. Contemporary psychiatric practice inherits epistemological frameworks that continue to privilege clinical observation over patient testimony. When a patient reports that a medication is causing intolerable side effects but objective measures show symptom improvement, whose assessment carries more weight? When someone describes their unusual perceptual experiences as spiritually meaningful but clinicians interpret them as psychotic symptoms requiring treatment, who has authority to determine the meaning of the experience? These are not merely philosophical questions but practical dilemmas that shape treatment decisions, research priorities, and the lived experiences of millions of people navigating mental health systems. The historical pattern of silencing patient voices has created a knowledge base about mental illness that is fundamentally incomplete, skewed toward what is observable and measurable by clinicians rather than what is experienced and meaningful to patients themselves.

Recovering patient voices from historical archives requires detective work and interpretive sophistication. Asylum records contain traces of patient perspectives even when they were not intended to preserve them. Discharge notes sometimes quote patient statements verbatim; incident reports document acts of resistance; letters intercepted by asylum staff reveal patients' own interpretations of their situations. Historian Barbara Taylor's work on her own psychiatric treatment and her historical research demonstrates how reading asylum records against the grain can recover patient agency and meaning-making even from documents designed to deny them[4]. This methodology involves asking not just what the records say about patients, but what they reveal about institutional power, what they inadvertently preserve despite their intentions, and what silences and absences might themselves be meaningful.

Patient voices matter because they reveal dimensions of psychiatric history that are invisible from the perspective of institutional authority. They show how diagnostic categories were experienced by those classified within them, how treatment practices affected those subjected to them, and how individuals maintained identity and agency within systems designed to reduce them to cases. Patient narratives document the creativity and resilience with which people navigated impossible situations, the communities of solidarity formed within institutions, and the alternative frameworks for understanding mental difference that persisted despite medical authority. Perhaps most importantly, patient voices challenge the teleological progress narrative that dominates psychiatric history—the story that moves inevitably from ignorance to knowledge, cruelty to compassion, confinement to community care. From patient perspectives, this narrative is far more ambiguous, with each reform bringing new forms of control alongside genuine improvements, and with fundamental questions about autonomy, coercion, and the right to be different remaining unresolved.

For you as a student of medicine or psychology, engaging with patient voices is not an optional supplement to clinical training but an ethical necessity. The patients you will encounter are not simply collections of symptoms to be managed but persons with their own interpretations of their experiences, their own goals for treatment, and their own assessments of what constitutes improvement or recovery. Learning to listen to patient narratives—not as data to be extracted but as testimony to be honored—requires unlearning some of the epistemic habits that medical education instills. It means recognizing that clinical expertise and lived experience are different forms of knowledge, both valuable, neither complete on its own. It means developing what philosopher Havi Carel calls epistemic trust—the willingness to accept that patients may know things about their conditions that are not accessible through clinical observation[5]. This book provides tools for developing that trust while maintaining critical analytical skills.

The Narrative Turn: From Medical Records to First-Person Accounts

The narrative turn in medical humanities emerged in the 1980s and 1990s as scholars across disciplines began recognizing that illness is not simply a biological phenomenon but a lived experience that people interpret, communicate, and integrate into their life stories. Physician and literary scholar Rita Charon coined the term narrative medicine to describe clinical practice that honors the stories patients tell about their illnesses, recognizing that these narratives contain essential information for diagnosis, treatment, and healing that cannot be captured in standardized medical records[6]. In psychiatry specifically, the narrative turn challenged the dominance of the biomedical model by demonstrating that mental illness cannot be fully understood through neurobiology and symptom checklists alone—the subjective experience of distress, the social contexts that shape it, and the meanings individuals assign to their experiences are equally essential to understanding.

The shift from medical records to first-person accounts represents a fundamental epistemological change in how we approach psychiatric knowledge. Traditional medical records are written in what anthropologist Byron Good calls the language of biomedicine—a specialized discourse that transforms the messy complexity of human suffering into standardized categories, objective measurements, and treatment protocols[7]. This transformation is not neutral but involves systematic exclusions and reinterpretations. Consider how a patient's statement I feel like I'm being watched by forces trying to control my thoughts becomes documented as Patient reports paranoid ideation and ideas of reference. The medical record captures the clinical significance but loses the phenomenological texture—the fear, the uncertainty about what's real, the struggle to make sense of disturbing experiences. First-person accounts preserve this texture, allowing readers to understand not just what symptoms someone had but what it felt like to have them.

First-person psychiatric narratives take multiple forms, each offering different insights and raising different methodological questions:

  • Asylum memoirs: Published accounts by former patients describing their experiences of confinement, treatment, and (sometimes) recovery, often written explicitly to expose institutional abuses or challenge psychiatric authority
  • Illness memoirs: Contemporary first-person books about living with mental illness, typically written after achieving some stability and offering retrospective interpretation of experiences
  • Patient letters and diaries: Documents written during acute episodes or hospitalization, offering immediate rather than retrospective perspectives but often fragmentary and difficult to interpret
  • Oral histories: Recorded interviews with psychiatric survivors, allowing for dialogue and clarification but shaped by the interview context and relationship
  • Collaborative autoethnography: Research approaches where people with lived experience of mental illness are co-researchers rather than subjects, analyzing their own experiences using academic frameworks
  • Digital narratives: Blogs, social media posts, and online communities where people share experiences in real-time, creating new forms of collective narrative and mutual support
Each form has strengths and limitations that you must consider when using them as sources of knowledge about mental illness and psychiatric treatment.

The methodological challenges of working with first-person psychiatric narratives are significant and must be addressed directly rather than ignored. How do we interpret accounts written during states of extreme distress or altered perception? Should we take them at face value, or do we need to correct for the effects of illness on perception and memory? But who decides what counts as distortion versus alternative interpretation? Literary scholar Susannah B. Mintz argues that the impulse to read psychiatric narratives for accuracy or reliability misses the point—these texts are valuable precisely because they show how individuals make meaning from experiences that exceed conventional frameworks of understanding[8]. The goal is not to determine whether someone's interpretation of their experience is objectively correct but to understand how they arrived at that interpretation and what it reveals about the experience itself.

One powerful example of the narrative turn's impact is the emergence of the Hearing Voices Movement, which began in the Netherlands in the 1980s when psychiatrist Marius Romme encountered a patient, Patsy Hage, who challenged his assumption that her voices were meaningless symptoms to be eliminated. Hage insisted her voices had meaning and content that needed to be understood rather than suppressed. This encounter led Romme to survey voice-hearers and discover that many people hear voices without distress or dysfunction, and that those who are distressed often find meaning-making approaches more helpful than medication alone[9]. The movement now operates internationally, creating spaces where voice-hearers share their experiences and develop their own frameworks for understanding and coping with voices. This represents a direct challenge to psychiatric epistemology: rather than accepting that only clinicians can interpret the meaning of symptoms, voice-hearers claim authority over their own experiences.

The narrative turn has also revealed how psychiatric diagnosis itself functions as a narrative framework that shapes how people understand and tell their own stories. When someone receives a diagnosis of bipolar disorder or borderline personality disorder, they often retrospectively reinterpret their life history through that diagnostic lens, identifying earlier experiences as symptoms they didn't recognize at the time. Sociologist David Karp's research on depression narratives shows how people incorporate psychiatric categories into their identity narratives, sometimes finding them helpful for making sense of confusing experiences, other times experiencing them as limiting or stigmatizing[10]. This raises important questions: Do diagnostic categories help people understand themselves, or do they impose medical interpretations that obscure other possible meanings? The answer appears to be both, depending on context, timing, and the individual's relationship to medical authority.

For your development as a clinician or researcher, the narrative turn offers practical tools for more ethical and effective practice. Narrative competence—the ability to listen carefully to patient stories, recognize their narrative structures and meanings, and respond in ways that honor the patient's perspective—has been shown to improve therapeutic alliance, treatment adherence, and patient satisfaction[11]. This doesn't mean abandoning clinical expertise or accepting every patient interpretation uncritically, but rather developing what we might call narrative humility—recognizing that your clinical understanding is one perspective among others, valuable but not omniscient. The chapters that follow will develop your capacity for this kind of engaged, critical listening, showing you how to read patient narratives for the insights they offer while remaining aware of the complex power dynamics and interpretive challenges involved.

How This Book Is Organized: A Guide to Reading the Anverse

This book is structured to move you progressively deeper into engagement with patient perspectives on psychiatric history and practice, beginning with broad historical and theoretical frameworks before focusing on specific methodologies and contemporary applications. The organization reflects a pedagogical philosophy: you need to understand the historical construction of psychiatric authority and the epistemological assumptions underlying it before you can fully appreciate why patient narratives challenge those foundations. Each chapter builds on previous ones while also standing alone as an exploration of a specific theme, allowing you to read selectively based on your interests while also following the cumulative argument about why centering patient voices transforms psychiatric understanding.

The first section of the book (Chapters 1-3) establishes historical and theoretical foundations by examining how madness has been constructed as an object of medical knowledge and institutional control. Chapter 1 traces the genealogy of madness from pre-modern spiritual and communal frameworks through the emergence of psychiatric authority in the eighteenth and nineteenth centuries, showing how diagnostic categories have evolved in response to changing cultural anxieties and social structures. Chapter 2 examines psychiatric epistemology—the ways psychiatry claims to produce knowledge about mental illness—and introduces alternative epistemological frameworks including phenomenology and neurodiversity perspectives. Chapter 3 analyzes the asylum as an institution, exploring how architecture, surveillance, and administrative practices enforced psychiatric authority while systematically erasing patient voice. Together, these chapters provide the historical context necessary for understanding why recovering patient narratives is both methodologically challenging and ethically essential.

The middle section (Chapters 4-8) focuses on patient narratives themselves and the social contexts that shaped them. Chapter 4 provides methodological guidance for reading asylum memoirs and other first-person accounts, teaching you how to analyze these texts as both historical evidence and literary artifacts. Chapter 5 explores phenomenological approaches to understanding madness, examining how individuals experience and describe states that exceed conventional frameworks of perception and meaning. Chapter 6 analyzes the social construction of mental illness, showing how cultural attitudes, power relations, and economic systems determine what behaviors are labeled pathological. Chapter 7 examines resistance movements including anti-psychiatry and contemporary Mad Pride activism, documenting how patients and psychiatric survivors have contested medical authority. Chapter 8 traces the history of deinstitutionalization, analyzing both its promises and failures from patient perspectives. These chapters immerse you in the complexity and diversity of patient experiences, challenging any simplistic narratives about psychiatric progress or patient victimization.

The final section (Chapters 9-12) explores contemporary frameworks and future directions for more ethical psychiatric practice and research. Chapter 9 examines neurodiversity and Mad Studies as alternative paradigms for understanding mental difference, moving beyond deficit models toward appreciation of cognitive diversity. Chapter 10 introduces narrative bioethics and personalistic care approaches, providing ethical frameworks for clinical practice that center patient dignity and agency. Chapter 11 analyzes recovery narratives, exploring how individuals navigate and transcend diagnostic categories through their own meaning-making processes. Chapter 12 examines how madness is represented in literature and media, providing tools for critical analysis of psychiatric discourse. The conclusion synthesizes these themes into practical guidance for developing what we call an ethics of listening—an approach to psychiatric practice and research grounded in genuine engagement with patient perspectives.

Throughout the book, you'll encounter several recurring analytical frameworks that structure the engagement with patient narratives:

  • Power analysis: Examining how institutional authority, professional expertise, and social hierarchies shape whose voice is heard and whose knowledge counts
  • Discourse analysis: Analyzing the language used to describe madness and mental illness, recognizing how terminology reflects and reinforces particular understandings
  • Phenomenological attention: Focusing on the subjective, lived experience of mental states rather than only their observable manifestations or biological correlates
  • Historical contextualization: Situating patient narratives within their specific historical, cultural, and institutional contexts to understand what they reveal about those contexts
  • Ethical reflection: Considering the moral implications of psychiatric practices, research methods, and knowledge claims, particularly regarding autonomy, dignity, and justice
  • Intersectional analysis: Recognizing how psychiatric authority intersects with other systems of power including gender, race, class, sexuality, and disability
These frameworks are not rigid methodologies but flexible tools for critical engagement with complex materials.

The book employs several pedagogical features designed to support your learning and critical thinking. Each chapter includes specific examples drawn from historical and contemporary sources, allowing you to see how theoretical concepts apply to actual cases. Blockquotes highlight particularly significant patient statements or analytical insights that deserve careful attention. Footnotes provide citations for further reading and indicate where you can find primary sources for your own research. The chapters build progressively in complexity, assuming that you're developing both knowledge and analytical skills as you proceed. Early chapters provide more historical background and methodological guidance; later chapters assume familiarity with key concepts and focus on applying them to contemporary questions.

You should approach this book with what we call critical empathy—a stance that combines emotional openness to patient experiences with analytical rigor about the contexts and power relations that shaped them. Critical empathy means taking patient narratives seriously as sources of knowledge while also recognizing that they are shaped by the circumstances of their production, the intended audiences, and the narrative conventions available to their authors. It means being moved by accounts of suffering and injustice while also analyzing the structural conditions that produced them. It means recognizing your own position within systems of psychiatric authority—as a future clinician, researcher, or mental health professional—and considering how that position shapes your reading and interpretation. This is challenging work that may sometimes feel uncomfortable, particularly when it reveals how psychiatric practices you're being trained to perform have been experienced as harmful by those subjected to them.

The book's title, The Anverse of Mirror, suggests that understanding psychiatric history requires looking at both sides of the reflective surface—the official narrative of medical progress and the hidden history of patient experience. But the metaphor goes deeper: mirrors don't simply reflect reality; they reverse it, showing a world that looks familiar but is fundamentally inverted. Patient narratives similarly invert conventional psychiatric narratives, showing familiar concepts like treatment, recovery, and care from perspectives that make them strange and newly visible. This defamiliarization is productive—it allows you to see assumptions and power relations that are invisible when you look only from the perspective of institutional authority. The goal is not to replace one narrative with another but to develop the capacity to hold multiple perspectives simultaneously, recognizing their tensions and contradictions as sources of insight rather than problems to be resolved.

As you read, you'll notice that the book doesn't offer simple answers or prescriptive solutions to the ethical and practical dilemmas it raises. This is intentional. The questions at the heart of psychiatric practice—How do we balance autonomy and beneficence when someone's judgment seems impaired? Who has authority to determine the meaning of unusual experiences? How do we provide care without imposing control?—don't have universal answers that apply in all contexts. What this book offers instead is frameworks for thinking through these questions more carefully, historical knowledge about how they've been addressed in the past, and patient perspectives that reveal dimensions of the questions that clinical training often obscures. Your task is to develop your own ethical stance, informed by this material but responsive to the specific contexts in which you'll practice. The conclusion provides guidance for this ongoing work of ethical development, but the real work happens in your engagement with the material throughout the book and in your future practice.

Back to contents

Notes

Introduction

  1. 1. Roy Porter, "The Patient's View," Theory and Society: 175-198, 1985
  2. 2. Packard and Elizabeth P.W, The Prisoners' Hidden Life, or Insane Asylums Unveiled, Chicago: Published by the Author, 1868
  3. 3. Miranda Fricker, Epistemic Injustice, Oxford University Press, 2007
  4. 4. Barbara Taylor, The Last Asylum, University of Chicago Press, 2014
  5. 5. Havi Carel and Ian James Kidd, "Epistemic Injustice in Healthcare," Medicine, Health Care and Philosophy: 529-540, 2014
  6. 6. Rita Charon, Narrative Medicine, Oxford University Press, 2006
  7. 7. Byron J. Good, Medicine, Rationality, and Experience, Cambridge University Press, 1994
  8. 8. Susannah B. Mintz, Unruly Bodies, University of North Carolina Press, 2007
  9. 9. Marius Romme and Sandra Escher, Accepting Voices, MIND Publications, 1993
  10. 10. David A. Karp, Speaking of Sadness, Oxford University Press, 1996
  11. 11. Trisha Greenhalgh and Brian Hurwitz, Narrative Based Medicine, BMJ Books, 1998

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