Epistemic Injustice in Healthcare
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Epistemic Injustice in Healthcare
  • Home
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    • EPIC Seminar series
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Epic Seminar series: all available online

Professor Máiréad Enright

Professor Máiréad Enright

Professor Máiréad Enright

30.06.25

1pm - 2:15pm


Further details TBC


  



Dr Silvia Ivani

Professor Máiréad Enright

Professor Máiréad Enright

19.05.25

2:30pm - 3:45pm


Further details TBC


  



Dr Tom Porter

Professor Máiréad Enright

Dr Tom Porter

28.04.25


  Disability benefits, epistemic sabotage, and the politics of knowing disability


Disability benefits have long been a focal point of political debate, with successive governments seeking to restrict access and tighten eligibility through reforms to assessment procedures. This presentation outlines research into disability benefits

28.04.25


  Disability benefits, epistemic sabotage, and the politics of knowing disability


Disability benefits have long been a focal point of political debate, with successive governments seeking to restrict access and tighten eligibility through reforms to assessment procedures. This presentation outlines research into disability benefits, focusing on the impact of reforms to Personal Independence Payment (PIP) and Universal Credit. Anti-welfare narratives depict welfare systems as overly-permissive, open to fraud, and fundamentally unfair. Countering these supposed ills have been political appeals to evidence and reforms made to disability benefit assessments in pursuit of a particular ideal – procedural objectivity. This presentation will outline the politics of objectivity within welfare reform, and will detail epistemic sabotage within benefit claims, whereby the knowledge claims of claimants and their personal health professionals are systematically disqualified. This work builds upon a tradition of scholarship examining disability as an administrative category (Stone 1985), which considers how the boundaries of legitimate need shift according to political economic and cultural circumstances. To this tradition I connect more recent scholarship on epistemic injustice and examine how identity, embodiment and social position shape practices of knowing disability.




Dr Jay Watts

Dr Lucienne Spencer

Dr Tom Porter

24.03.25

  

Epistemic Injustice and Psychiatric Diagnosis: Who Gets to Be Believed?  


  Few topics in mental health spark more controversy than psychiatric diagnosis. From ward rounds to social media and the broadsheet press, debates are often heated, polarising, and destructive. Yet these discussions frequently treat all psychiatric diagnos

24.03.25

  

Epistemic Injustice and Psychiatric Diagnosis: Who Gets to Be Believed?  


  Few topics in mental health spark more controversy than psychiatric diagnosis. From ward rounds to social media and the broadsheet press, debates are often heated, polarising, and destructive. Yet these discussions frequently treat all psychiatric diagnoses as if they function the same way—but they do not. Diagnoses like depression often confer credibility, opening doors to care and support. Others, like schizophrenia and borderline personality disorder, are far more likely to strip patients of epistemic agency, determining whose voices are heard and whose suffering is dismissed. Even within the same diagnosis, experiences diverge: for some, a label provides meaning and empowerment; for others, it is an act of epistemic violence. Efforts to challenge psychiatric categorisation, however, risk slipping into accusations of false consciousness, where those who do not accept or reject their diagnosis in the 'correct' way are framed as simply mistaken. I argue that epistemic injustice provides a crucial framework for navigating this complexity, allowing us to critique diagnosis while respecting the varied meanings patients ascribe to their diagnoses. By centering patient epistemic agency, we can develop more just approaches to future psychiatric nosologies.



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Dr Fred Cooper

Dr Lucienne Spencer

Dr Lucienne Spencer

27.01.25


Title: Woman Alone: Carmita Wood's archival fragments and the emotions of epistemic injustice


In the summer of 1975, the inaugural issue of the feminist journal Labor Pains carried a brief article, ‘Woman Alone’, written by a victim - and co-articulator - of sexual harassment, Carmita Wood. Harassed by a professor of Nuclear Physic

27.01.25


Title: Woman Alone: Carmita Wood's archival fragments and the emotions of epistemic injustice


In the summer of 1975, the inaugural issue of the feminist journal Labor Pains carried a brief article, ‘Woman Alone’, written by a victim - and co-articulator - of sexual harassment, Carmita Wood. Harassed by a professor of Nuclear Physics, Boyce McDaniel, at Cornell University, Wood had turned to feminist scholars and activists in Cornell’s Human Studies department to help her make sense of what she had experienced; not (or not exclusively) to herself, but in her ongoing attempts to provide evidence that she had left her post at the university for good reason. The work they did together resulted in the formation of a campaigning organisation, Working Women United (WWU), with Labor Pains as its organ, and the contribution of a new composite term, sexual harassment, to stake out a particular set of behaviours and experiences which had been hitherto difficult to formally name.  For many if not most scholars of epistemic injustice (and a smaller number of scholars of sexual harassment and second-wave feminism), Wood’s story is at least partially familiar, forming a central spur of Miranda Fricker’s famous 2007 analysis of hermeneutic injustice. Amid sustained and ongoing discussions over what Wood ‘knew’ about her experience, however, there has been far less attention paid to what she said – and how she felt – at the time. In ‘Woman Alone’, and in a speak-out on sexual harassment attended by hundreds, Wood (and her fellow speakers) made sense of their experiences – and the epistemic problems of understanding and speaking about them – through the interconnecting prisms of aloneness and shame. I take their emphasis on the emotional barriers to epistemic action as a prompt for a consideration of the emotions that attend experiences of epistemic injustice, re-centring them as primary mechanisms rather than secondary harms.


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Dr Lucienne Spencer

Dr Lucienne Spencer

Dr Lucienne Spencer

25.11.24


Epistemic Pedantry in the Dementia Context

 

Imagine the following scenario: A person with dementia tells a care worker that a certain loved one visited them yesterday. The care worker replies that the resident is mistaken and that this particular loved one has passed away.

Imagine a second scenario: A person with dementia starts wis

25.11.24


Epistemic Pedantry in the Dementia Context

 

Imagine the following scenario: A person with dementia tells a care worker that a certain loved one visited them yesterday. The care worker replies that the resident is mistaken and that this particular loved one has passed away.

Imagine a second scenario: A person with dementia starts wishing everyone a merry Christmas, and sings Christmas songs. A family member informs the person with dementia that it is not Christmas.

Through this talk, I explore the epistemic harm of contradicting false beliefs in the context of dementia. Drawing on Kant, I attempt to capture this epistemic harm through a distinct form of epistemic injustice which I call 'epistemic pedantry': where a person’s epistemic status is unnecessarily undermined in pursuit of a trivial truth.


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Dr Charlotte Blease and Dr Jo Hunt

Dr Charlotte Blease and Dr Jo Hunt

Dr Charlotte Blease and Dr Jo Hunt

28.10.24


Title: Epistemic injustice, healthcare disparities and the missing pipeline: reflections on the exclusion of  disabled scholars from health research 

  

People with disabilities often face unfair treatment in both healthcare and society. To improve healthcare and make it more inclusive, research must focus on the unique challenges f

28.10.24


Title: Epistemic injustice, healthcare disparities and the missing pipeline: reflections on the exclusion of  disabled scholars from health research 

  

People with disabilities often face unfair treatment in both healthcare and society. To improve healthcare and make it more inclusive, research must focus on the unique challenges faced by disabled people. Since they have firsthand experience, disabled individuals are in a strong position to identify problems and suggest improvements in healthcare that others might miss. Academic research informed by patients could play a key role in highlighting these perspectives, and with the right policy support, these insights could help shape better healthcare practices and public life.
 

Despite the clear benefits of including disabled voices in research, we explore the barriers that disabled people in the UK face when trying to conduct health research. In this paper, we draw on previous research and the personal experience of one of the authors - Joanne Hunt, who has spent over three years trying to find a suitable and accessible PhD program while dealing with energy-limiting conditions and being mostly homebound.
 

First, we look at the broader issue of how knowledge from disabled people is often undervalued in health research. Second, we focus on how disabled researchers experience exclusion, using ideas from philosophers Kidd and Carel (2017) on ‘strategies of exclusion.’ Finally, we suggest ways to reduce these barriers and improve access for disabled researchers in academia.



Professor Richard Pettigrew

Dr Charlotte Blease and Dr Jo Hunt

Dr Charlotte Blease and Dr Jo Hunt

30.09.24


Title:   

What is the characteristic wrong of testimonial injustice? 

  

My aim in this paper is to identify the wrong that is done in all cases of testimonial injustice, if there is one. Miranda Fricker (2007) proposes one account of this distinctive wrong, and Gaile Pohlhaus Jr. (2014) offers another. I think neither works. Nor doe

30.09.24


Title:   

What is the characteristic wrong of testimonial injustice? 

  

My aim in this paper is to identify the wrong that is done in all cases of testimonial injustice, if there is one. Miranda Fricker (2007) proposes one account of this distinctive wrong, and Gaile Pohlhaus Jr. (2014) offers another. I think neither works. Nor does an account based on giving due respect to the testifier’s epistemic competence. Nor does an account based on exposing the testifier to substantial risk of harm. Rachel Fraser (2023) describes a further account, and the proposal I favour is a slight amendment of this.




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Dr Naomi Kloosterboer

Dr Charlotte Blease and Dr Jo Hunt

Dr Naomi Kloosterboer


How to take seriously a person with extreme beliefs 

24.06.24

  

To understand the subjectivity of a person with extreme beliefs, we need to take them seriously. Intuitively, taking another person seriously involves open-minded engagement. But in the case of extreme views such as The Great Replacement theory, open-mindedness not only seems 


How to take seriously a person with extreme beliefs 

24.06.24

  

To understand the subjectivity of a person with extreme beliefs, we need to take them seriously. Intuitively, taking another person seriously involves open-minded engagement. But in the case of extreme views such as The Great Replacement theory, open-mindedness not only seems unrealistic, but also irrational or even immoral. Although some opt for closed-minded engagement instead, I will argue that we need to move from open-mindedness to epistemic openness. Taking the other seriously involves dealing with how our own perspective distorts understanding the other, (i) in listening, (ii) in language, and (iii) in the context. I will extend my argument to the medical context and reflect on how to apply this to the relation between a physician and a patient suffering from mental illness. Such a patient may in some cases harbour extreme beliefs but in other cases have (radical) different experiences and perspective.




Dr Maru Mormina

Professor Miranda Fricker

Dr Naomi Kloosterboer


Epistemic injustice and epistemic responsibility in evidence-informed policymaking during crises

20.05.24


Complex and interrelated crises define today’s policy space and pose particular challenges for deploying science to support evidence-informed policymaking (EIPM). Pandemics, climate change, natural catastrophes or energy crises demand 


Epistemic injustice and epistemic responsibility in evidence-informed policymaking during crises

20.05.24


Complex and interrelated crises define today’s policy space and pose particular challenges for deploying science to support evidence-informed policymaking (EIPM). Pandemics, climate change, natural catastrophes or energy crises demand science-based solutions, but also expose our inability to locate, discriminate, understand, and respond to incomplete and contested evidence. The reification of scientific knowledge and expertise as the antidote to uncertainty obscures the challenges of deciding what needs to be asked, and ‘which’ or ‘whose’ science ought to provide the answers when contestation and disagreements emerge. This highlights the inevitability of ignorance in crisis policymaking, created by the exclusion - but also inclusion- of voices, facts and values from the decision-making processes.

In this talk, I will use examples from the past COVID-19 pandemic to show how scientific expertise was selectively and narrowly mobilised to respond to the crisis, thus creating a form of systemic ignorance that shaped public policy. Following the work of Elizabeth Anderson, I argue that explaining why expertise is so narrowly conceived and mobilised requires us to consider science’s structural epistemic injustices. I will finish by sketching an account of epistemic responsibilities that may allow epistemic communities to widen the range of voices contributing to the policy process despite the inherently exclusionary nature of expertise.  Taking epistemic responsibility seriously can help address the root causes of epistemic injustices in EIPM and pave the way for more inclusive and deliberative forms of crisis governance better equipped to deal with uncertainty.



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Professor Lauren Freeman

Professor Miranda Fricker

Professor Miranda Fricker

Epistemic Microaggressions and Epistemic Harm in Medicine

29.04.24


Drawing on her recently published book, Microaggressions in Medicine (Oxford 2024), this talk will provide an overview and analysis of epistemic microaggressions in medical contexts. Epistemic microaggressions result in epistemic harm to recipients. Focusing on cases of pati

Epistemic Microaggressions and Epistemic Harm in Medicine

29.04.24


Drawing on her recently published book, Microaggressions in Medicine (Oxford 2024), this talk will provide an overview and analysis of epistemic microaggressions in medical contexts. Epistemic microaggressions result in epistemic harm to recipients. Focusing on cases of patients who are members of marginalized groups, the presentation will demonstrate how epistemic microaggressions can lead to a variety of serious short- and long-term harms to patients and therefore ought to be avoided by healthcare professionals. Special attention will be paid to the moral significance of epistemic microaggressions in medical contexts.





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Professor Miranda Fricker

Professor Miranda Fricker

Professor Miranda Fricker

Epistemic Injustices and Mental Ill-Health

04.03.24


I will talk us through some types of epistemic injustice, principally: ‘testimonial injustice’, ‘pre-emptive testimonial injustice’, and ‘hermeneutical injustice’ which I defined in earlier work; and ‘testimonial smothering’ as defined by Kristie Dotson. I’ll explain these phenomena largel

Epistemic Injustices and Mental Ill-Health

04.03.24


I will talk us through some types of epistemic injustice, principally: ‘testimonial injustice’, ‘pre-emptive testimonial injustice’, and ‘hermeneutical injustice’ which I defined in earlier work; and ‘testimonial smothering’ as defined by Kristie Dotson. I’ll explain these phenomena largely by way of examples from a memoir of mental ill-health written by the British actor David Harewood, Maybe I Don’t belong Here: A Memoir of Race, Identity, Breakdown and Recovery (2021). His personal story explores how experiences of racism, growing up in Britain in the seventies and as a young man in the eighties, sowed the seeds of personal fracture and psychological disconnect that later expressed themselves in psychosis.

I will also reflect that many psychiatrists and therapists effectively see their own work as including the amelioration of precisely these forms of epistemic injustice: aiming to create a therapeutic relationship in which credibility is not withheld, and shared intelligibility of experience is cultivated, with the result that the service-user may come to express themselves without needing to truncate or restyle what they want to say. This may be an impossible ideal, given that healthcare professionals must equally be diagnostically alert to fantasy, projection, and delusion, among other phenomena of epistemic disturbance, but impossible ideals can nonetheless be useful guiding ideals, playing a helpful informal self-regulatory role in one’s professional practice. If so, then perhaps the explicitly epistemic framing of this particular guiding ideal may make for a useful tool in the therapeutic toolbox?


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Funded by Wellcome


This project was generously funded by wellcome. Grant : [226603/Z/22/Z], 'EPIC: Epistemic Injustice in Health Care'.

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