Interview with Naru Fukuchi

As part of our ongoing content, we feature authors who have published in Culture, Medicine, and Psychiatry.

Today, we are excited to bring you our interview with Naru Fukuchi!

What is your article “Children’s Everyday Actions After Disaster: Cultural Meaning, Developmental Timing, and Moral Agency in Post-disaster Japan” about?

This article explores how children’s everyday behaviors after the Great East Japan Earthquake can be understood not simply as symptoms or “problem behaviors,” but as culturally and developmentally meaningful adaptations.

After the disaster, I visited schools, evacuation shelters, and temporary housing sites throughout Miyagi Prefecture. There, I observed children quietly playing video games together, hiding shoes, giving away sweets, and showing unusual reactions around food and money. At first, I interpreted these behaviors from a psychiatric perspective. However, over time, I began to feel that symptom-based explanations alone were insufficient.

For example, the repeated “shoe hiding” behavior initially appeared to be simple mischief. But when teachers and I explored the behavior more carefully, it seemed that children were repeatedly recreating the emotional experience of “losing something important and finding it again.” Through play, they may have been trying to restore a sense of safety and predictability.

In this article, I interpret these behaviors through the lenses of cultural psychiatry, developmental psychology, and medical anthropology. I wanted to suggest that children are not only passive victims of disaster, but also active participants in rebuilding meaning, morality, and relationships within their communities.

Tell us a little bit about yourself and your research interests.

I originally began my career as a pediatrician before moving into psychiatry, and I now work as an Associate Professor in the Department of Psychiatry, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, where I practice as a child and adolescent psychiatrist in Japan. During graduate school, I specialized in public health and conducted epidemiological research on suicide within communities.

Because of this background, I have long been interested not only in individual psychiatric symptoms, but also in community mental health and the social environments that shape people’s wellbeing.

After the Great East Japan Earthquake in 2011, I joined outreach teams that visited evacuation shelters and temporary housing sites. Later that same year, the Miyagi Disaster Mental Health Care Center was established, and I became one of its founding members. Eventually, I served as the director of the center.

Even now, fifteen years after the disaster, I continue to conduct home visits and school visits in affected communities. Recovery is not simply about rebuilding infrastructure; it is also about how relationships, daily life, trust, and cultural meaning are gradually reconstructed over time.

My research interests include disaster mental health, child and adolescent psychiatry, community mental health, cultural psychiatry, and medical anthropology. I am especially interested in how culture shapes the ways people suffer, recover, connect with others, and rebuild meaning after crises.

What drew you to this project?

Immediately after the earthquake, I entered the field primarily as a child psychiatrist. I was trained to observe psychiatric symptoms and trauma-related reactions, and initially I approached the children in that way.

However, in schools and shelters, I repeatedly encountered situations that could not be fully explained through symptom-based psychiatry alone. There were many phenomena that only became understandable when viewed at the level of the community, relationships, and Japanese society more broadly.

At the same time, I had opportunities to learn about disaster recovery processes in other countries. Through those experiences, I gradually realized how deeply culture and mental health are connected. Every society has its own ways of expressing distress, maintaining relationships, and restoring meaning after disasters.

This led me to ask broader questions: What aspects of Japanese post-disaster recovery are culturally shaped? How are ideas such as harmony, reciprocity, endurance, and collective responsibility formed? And what kinds of support actually help communities recover in culturally meaningful ways?

I also conduct quantitative research and statistical analyses, and I value evidence-based approaches very much. But I began to feel that some realities cannot be fully captured through numbers alone. I wanted to share the interpretations and questions that emerged from my field experiences and invite others to think about them together.

What was one of the most interesting findings?

One of the most memorable experiences for me was the “shoe hiding” phenomenon described in the article.

Teachers at several schools noticed that children were repeatedly hiding each other’s indoor shoes. They felt that something about the behavior was unusual, but they could not fully explain why. Even I initially thought, “This probably has nothing to do with the disaster.”

However, as we explored the behavior together, it gradually became clear that many psychological and symbolic meanings might be embedded within it. The children had all experienced sudden loss during the tsunami. Important things had disappeared instantly and unpredictably.

I eventually began to understand the repeated cycle of “losing and finding” as a form of post-traumatic play.

There is actually a story I did not include in the paper. At one point, we intentionally introduced a playful “Easter egg” activity in which children hid and found objects together within a structured game. Interestingly, after that experience, the shoe hiding behavior almost completely disappeared.

That experience left a deep impression on me. It reminded me that children often recover through play, relationships, and shared meaning-making rather than through direct verbal explanation alone.

What are you reading, listening to, and/or watching right now?

Recently, I have become very interested in LEGO® Serious Play®. Rather than simply building objects for fun, it is a method that uses LEGO to support communication, reflection, therapy, and team building. I also became a certified facilitator.

I use it in work with children, families, and professional teams. Through these experiences, I have increasingly felt that individual treatment alone has limits. If we truly want to support mental health, we also need to create healthier environments, relationships, and communities.

I am also currently reading Reinventing Organizations by Frédéric Laloux, which explores how organizations can be structured around trust, self-management, and shared purpose rather than hierarchy and control. It resonates deeply with my growing interest in how communities and care systems can become more alive and human-centered.

This has made me think more deeply about how people build trust, form connections, and create spaces where they feel psychologically safe. Perhaps that is one reason why I was drawn to LEGO in the first place.

I have also been reading more works in medical anthropology and cultural psychiatry recently, especially writings that explore care, community, loneliness, and social connection in contemporary society.

If there was one takeaway or action point you hope people will get from your work, what would it be?

I hope readers will become a little more cautious about interpreting children’s behaviors too quickly as pathology or “symptoms.”

Children often express distress, recovery, morality, and hope in indirect ways. Sometimes these expressions appear through play, silence, sharing, rituals, or seemingly strange everyday behaviors.

I hope this work encourages people to ask not only “What symptoms does this child have?” but also “What meaning might this behavior hold within this child’s relationships, culture, and lived experience?”

Children are not simply passive victims after disasters. They are also active participants in rebuilding connection, meaning, and community.

Interview with Eugene Raikhel

As part of our ongoing content, we feature authors who have published in Culture, Medicine, and Psychiatry.

Today, we are excited to bring you our interview with Eugene Raikhel!

What is the article “What Crisis? Competing Narratives of Mental Health in US Higher Education “about?

The article draws on interviews that I conducted with mental health professionals who work with college students as part of a broader project on college mental health. Over the past few years we’ve collectively heard a lot about the “college mental health crisis” in popular discourse. In this article, I argue that mental health professionals have a range of very nuanced perspectives on the idea of a “college mental health crisis” and I trace five distinct ways in which they frame and understand the problem. Some of these framings stand in tension to one another, while others complement one another.

Tell us a little bit about yourself and your research interests.

I am a cultural, medical, and psychological anthropologist and an Associate Professor in the Department of Comparative Human Development at the University of Chicago. My research interests generally cluster around what philosopher Ian Hacking has called “looping effects” – the multiple ways in which forms of knowledge, particularly in the domain of psychiatry and mental health – come to shape the lives and actions of people who live under their classifications, and how these actions in turn come to transform expert knowledge. I’ve looked at such issues in a historical ethnography of addiction medicine in post-Soviet Russia, and I’m currently examining them in a study which asks how ideas and enactments of mental health and illness are transforming in higher education settings.

What drew you to this project?

A number of years ago, while teaching a course about culture and mental health, I noticed that students seemed to be speaking about their own experiences with mental illness conditions in ways that seemed novel to me. These certainly were not the conversations that I remembered from my own college experiences in the 1990s. There was more disclosure, but beyond that, more identification with diagnoses, and generally more complex engagement with the issues raised by labels, medications, talk therapy, and more. It seemed that something in the culture at large was changing and this peaked my ethnographic interest. The broader study that I’m working on, tentatively titled “Degrees of Distress: College and the Transformation of Mental Health,” emerged from these early observations.

What was one of the most interesting findings?

We tend to think of medicalization or psychiatrization as processes being driven at least in part by professionals working to expand their jurisdictions. According to this logic, you would think that the psy professionals involved in college mental health would be always trying to attract more students to the counseling center and place more types of conditions under the framework of what they properly address. And while this is certainly the case to some degree, I found that many mental health professionals working with college students, and particularly directors of counseling centers, were both contesting the medicalization of mental health and arguing for a way of addressing mental health issues which would use more of the whole campus. Part of this is because many counseling centers have found themselves struggling to address the demand for services for many years now, and people are increasingly thinking of how to distribute various forms of care throughout a college or university. But it is also the case that many counselors want to maintain a space for interacting with students around problems which are not medicalized from the start; rather than the aim of therapy being symptom reduction, they want students to be able to make meaning out of experiences which have challenged them. So there’s a kind of active resistance to the medicalization of mental health among many of the professionals which was very interesting to find.

What are you reading, listening to, and/or watching right now?

I’m reading Klara and the Sun by Kazuo Ishiguro, a novel told from the point of view of a humanoid robot with artificial intelligence. Given that my project has gotten me paying attention to the ways that some young people are increasingly turning to AI for help with mental health issues, as well as for various forms of companionship, this book has been great to think with.

If there was one takeaway or action point you hope people will get from your work, what would it be?

Simply that it is important to not reduce the problem of college mental health to individual psychopathology. Such a framing also assumes that the only intervention which needs to be made is at the individual level – providing more access to therapy and medication – and while these are important tools, many counselors clearly agree that they are not adequate to addressing this problem “upstream”. At the same time, it is also the case that these same counselors and counseling center directors don’t usually have the tools to address upstream and structural causes.

Interview with Alexander Brandt Ryborg Jønsson, Elizabeth Xiao-An Li and Anne Mia Steno

The next few months we’ll be highlighting authors who have published in Culture, Medicine, and Psychiatry.

Today, we are excited to bring you our interview with Mia, Elizabeth & Alex!

What is the article “Enacted Restoration of Selfhood: A Kierkegaardian Perspective on Self-harm Among People with Mental Illness” about?

The article is an exploration of the lived experiences of individuals engaging in non-suicidal self-harm and shows how self-harm is not only the experiential nexus of a complex relationship between the body and the world but also a mechanism for overcoming the self. Whereas self-harm within the context of mental illnesses has traditionally been researched and understood as symptomatic behavior, our contention is that self-harm can be described through the lens of ‘enacted selfhood’ as an analytical framework inspired by Søren Kierkegaard’s existential thought for shedding light on what more is at stake in self-harm among individuals living with mental illness.

Tell us a little bit about yourself and your research interests.

Alex: I’m a social anthropologist with a focus on critical analysis of mental health and health services, particularly overuse and overdiagnosis. My work examines how diagnostic categories, practices, and technologies are produced and negotiated, and how they shape lived experiences, sustain promissory visions of biomedicine and generate broader questions of inequality and care.

Anne Mia: I’m a social anthropologist working within social psychiatry and welfare institutions. My research focuses on people living at the margins of welfare systems, attending to experiences of loneliness, not belonging, and everyday life under institutional conditions. Grounded in phenomenological approaches to the body, I explore how lives are shaped through movements between spaces, relations, and forms of care. Methodologically, I work ethnographically and with multisensory approaches to make present forms of experience that are often rendered difficult to articulate, asking how they are navigated, resisted, and reworked in practice.

Elizabeth: I’m a philosopher of religion and a Kierkegaard scholar, with particular interest in his concept of existence and critiques of systematic philosophy, the problems of conceptuality, and the relation between religious faith and reason as well as the development of existential thought more generally in 19th and 20th century European philosophy and theology.

What drew you to this project?

This article is a collaborative and interdisciplinary project between the three of us, but it was developed over different stages. Alex and Anne Mia conducted different field works on two different projects, both centering on lived experiences with mental illness. We’ve known each other since our university days and often discuss theoretical or empirical challenges. We both became curious when we noticed how conversations with interlocutors about their experience and reflections on non-suicidal self-harm did not seem to reflect the way in which this phenomenon has traditionally/predominantly been treated in existing research. Here self-harm remains marginalized both analytically and empirically as it is viewed as a mere symptom among individuals living with mental illness or “call for help”. However, what we, Alex and Anne Mia, experienced in fieldwork, showed that there was something more at stake in the question of self-harm: It took up a lot of space in conversations with individuals who self harmed, who had profound and extensive reflections on the way they experienced this, thought about it, and enacted it with many expressing it to be an act of deep existential import.

Alex later invited Elizabeth to collaborate, after hearing her speak about Søren Kierkegaard at the Young Academy of the Danish Royal Society, which we are both fellows of. Upon discussing the project, it became clear to us that Kierkegaard’s concept of existence and selfhood and his proto-phenomenological and existential approach could offer a theoretical framework that could encompass/shed light on the individuality, existential complexities and the many ambiguous and paradoxical ways self-harm was reflected on and described by individuals in their lived experience of engaging in self-harm.

The article is thus the result of a discovering deeper and mutually illuminating connections between our research interests and bringing these together in this joint interdisciplinary effort.

What was one of the most interesting findings?

That self-harm is not merely a call for help or a means of translating or displacing psychological pain into physical sensation; rather, it may be understood as an example of what we term “enacted selfhood.” While the linguistic and discursive dimensions are often foregrounded within social recovery frameworks, this research underscores the importance of attending to concrete, embodied experience. The body, too, articulates meaning: self-harm constitutes a form of expression to which we ought to remain attentively and analytically responsive.

What are you reading, listening to, and/or watching right now?

Alex: I have been reading Glenn Bech’s Jeg anerkender ikke længere jeres autoritet (I No Longer Recognize Your Authority) which poetically explores experiences of societal inequality. I am the first in my family to even graduate from high school and his words really reflect my own experiences in childhood, but also broaden my understanding of the deep humanity present in the most difficult lives and fates among my interlocutors. I’ve been listening to Mahler’s “Symphony No. 3”, which I’ll be going to hear performed by Tivoli Copenhagen Phil & Odense Symphony Orchestra next month (and Elizabeth will join me!) but I generally like all kinds of music and am a very dedicated euphonium player in Copenhagen Brass Band.

Anne Mia: I am currently reading The Museum of Innocence by Orhan Pamuk, which explores the relationship between the affluent Kemal and the less privileged Füsun, and how Kemal assembles a collection of objects, such as one hundred cigarette butts, that come to narrate the story of their love. The novel simultaneously functions as a key to a physical museum, blurring the boundaries between fiction, materiality, and exhibition. Reading this work serves in part as inspiration for a current research grant application, as I am particularly interested in modes of dissemination and in how anthropological inquiry might intersect with aesthetics and literary form.

I have been listening extensively to Bach lately; and, as a mother, I have, perhaps less voluntarily, been accompanying my child’s engagement with Melodi Grand Prix, Denmark’s children’s version of Eurovision.

Elizabeth: I recently finished Ben Lerner’s new novel Transcription and just started re-reading Plato’s Dialogues. The next work of fiction I’ll be picking up is Anne Mia’s YA novel Akio from 2021, which very presciently explores a romantic relationship with an AI. As a Kierkegaard scholar, I’m endlessly fascinated with the struggles we humans have in communicating our thoughts and inner lives, and the ways in which our technology and media for communication can hinder and complicate our relationships with and understanding of ourselves and others. I keep coming back to Wagner’s Tristan und Isolde, but I have also been listening to a lot of David Bowie and Wet Leg these past weeks. In between comfort-(re)watching The Office and Gilmore Girls, my most recent trip to the cinema was to see Kristoffer Borgli’s The Drama.

If there was one takeaway or action point you hope people will get from your work, what would it be?

Not to dismiss or take for granted certain phenomena, behaviors or actions, but recognize the limits of categorization: As our exploration of self-harm shows it is necessary to take into account the individual and the particular context, which at the same time is not something we can simply understand and explain once and for all. As Kierkegaard underlines to try to turn human experience into circumscribed, universal concepts results in dissolving the reality we are attempting to grasp, because our concrete embodied existence as individuals is in movement.

Interview with Augustus Osborne

The next few months we’ll be highlighting authors who have published in Culture, Medicine, and Psychiatry.

What is the article “Embracing Pluralism: Rethinking Western Psychiatric Models for Equitable Global Mental Health” about?

This article is fundamentally a challenge to one of global health’s most comfortable assumptions: that what works in Boston or London will work in Freetown or Kampala, provided we translate it carefully enough. The global mental health movement has done genuinely important work in drawing attention to the enormous burden of mental illness in low- and middle-income countries up to 85% of people with mental health conditions in these settings receive no treatment at all. But in its urgency to close that treatment gap, the movement has largely exported Western psychiatric frameworks wholesale: the DSM diagnostic categories, pharmaceutical-centred treatment protocols, and individual psychotherapy as the gold standard of care.

My article argues that this approach carries real risks that are too often ignored. It can produce cultural mismatch where diagnostic tools built on Euro-American concepts of depression and anxiety fail to capture how distress is experienced and expressed in other societies. It can medicalise what is fundamentally social suffering, framing poverty, displacement, and structural injustice as individual disorders amenable to a prescription. And it can marginalise or displace indigenous healing systems traditional practitioners, religious leaders, community elders that communities trust and turn to.

The paper is not an argument against biomedical psychiatry. It is an argument for pluralism: a framework that values multiple healing traditions as equally legitimate, prioritises cultural adaptation and local leadership, and insists that equity not just coverage must be the measure of success. I draw on evidence from Zimbabwe’s Friendship Bench, community-based programmes in India and Pakistan, and hybrid models from Nepal and Uganda to show that locally grounded approaches are not second-best alternatives they are often more effective, more sustainable, and more meaningful to the people they serve.

Tell us a little bit about yourself and your research interests.

I am a public health researcher based in Freetown, Sierra Leone, where I was born and trained. I hold an MSc in Public Health and a BSc in Biological Sciences from Njala University, and I have spent the past decade trying to understand and generate evidence about the structural forces that shape health and illness in Sierra Leone and across sub-Saharan Africa.

My research spans a wide range of topics: maternal and child health, health systems strengthening, infectious disease, health equity, and increasingly, the intersection of digital health and social determinants of wellbeing. I have authored and co-authored over 140 peer-reviewed publications, and I used to teach Epidemiology and Biostatistics at Njala

University, where I tried to pass on not just statistical methods but a way of thinking about evidence who produces it, who it serves, and whose experiences it tends to miss.

What connects all of my work is a preoccupation with equity with understanding why health outcomes are so unequally distributed, and with generating the kind of evidence that can actually move policy in the right direction. I use a range of tools ArcGIS for spatial analysis, machine learning for predictive modelling, NVivo and MAXQDA for qualitative work but the driving question is always the same: who is being left behind, and why?

Mental health sits at a particularly important intersection of these concerns. In Sierra Leone, the legacy of a decade-long civil war, the Ebola epidemic, and chronic poverty has created an enormous burden of psychological distress yet mental health services remain desperately under-resourced, and the frameworks imported to address the gap do not always fit the realities of the people they are meant to serve.

What drew you to this project?

Honestly, it was the gap between what I observed in practice and what the global mental health literature was telling me should work.

Working in Sierra Leone first as a surveillance officer during the Ebola outbreak, then in health systems research I repeatedly encountered situations where people in psychological distress were navigating between multiple systems of care simultaneously: visiting a biomedical clinic, consulting a traditional healer, seeking counsel from a religious leader. This was not confusion or ignorance. It was a rational response to a plural reality, where different systems offered different things and no single framework captured the full picture of suffering or healing.

Yet the global mental health literature I was reading largely treated this pluralism as a problem to be overcome, a sign of inadequate access to proper care rather than as a resource to be understood and built upon. I found that framing both empirically questionable and, frankly, troubling in its assumptions about whose knowledge counts.

I was also struck by the growing body of evidence from programmes like Zimbabwe’s Friendship Bench, which showed that community-embedded, culturally resonant interventions could achieve outcomes comparable to or better than imported Western protocols. That evidence deserved a more prominent place in the conversation about how global mental health should be organized and funded. Writing this paper was my attempt to make that argument systematically drawing together the critique, the evidence, and a concrete set of recommendations in a way that might be useful to researchers, practitioners, and policymakers working in this space.

What was one of the most interesting findings?

The finding that most stayed with me and that I think has the broadest implications is the evidence around stigma. The dominant narrative in global mental health has long been that the biomedical model reduces stigma by framing mental illness as a brain disease rather than a moral failing or spiritual affliction. The logic is intuitive: if depression is a chemical imbalance, not a character flaw, people should be less blamed for it.

But the evidence I reviewed tells a more complicated story. In several settings, the introduction of Western psychiatric labels increased stigma because these diagnoses were experienced as foreign, permanent, and frightening in ways that local idioms of distress were not. In rural China, medicalizing depression led to greater social distancing, not less. In Sri Lanka, Western diagnostic terms for schizophrenia were associated with new forms of social exclusion. The assumption that biomedical framing is universally destigmatizing turns out to be empirically unfounded and it is an assumption that has shaped enormous amounts of global mental health investment.

This matters because it illustrates a broader point: the risks of exporting Western models are not just theoretical. They play out in real people’s lives, in communities where the introduction of a foreign framework can disrupt existing social networks, undermine indigenous coping strategies, and create new forms of harm even while trying to help. That is a finding that should give the global mental health movement serious pause.

What are you reading, listening to, and/or watching right now?

I am currently reading The Wretched of the Earth by Frantz Fanon which feels more relevant than ever to the questions this paper raises about knowledge, power, and whose frameworks get to count as universal. Fanon’s analysis of colonial psychiatry is remarkably prescient, and I find myself returning to it as a grounding text for thinking about decolonial approaches to global health.

In terms of listening, I have been following the Global Health with Greg Martin podcast, which does a good job of bringing together researchers and practitioners from the Global South in conversations that do not always make it into mainstream journals. There is something valuable about hearing researchers from Sierra Leone, Uganda, and Nepal speak in their own voices about the challenges and opportunities in their contexts.

And I have been watching with great interest and some anxiety about the ongoing debates about artificial intelligence in healthcare. My own research has moved increasingly into machine learning applications for public health, and the questions about bias, equity, and whose data trains the models feel very continuous with the questions I am raising in this paper about whose knowledge shapes global mental health frameworks.

If there was one takeaway or action point you hope people will get from your work, what would it be?

The one thing I most want readers to take away is this: pluralism is not a compromise it is a superior framework.

I am aware that pluralism can sound like a polite way of saying “let’s include everyone and not make hard choices.” That is not what I mean. I mean something more specific and more demanding: that the most effective, most equitable, and most sustainable approaches to global mental health are those that genuinely value multiple healing traditions as legitimate on their own terms not as supplements to biomedical care, not as cultural window-dressing on Western protocols, but as systems of knowledge and practice that have evolved to address human suffering in specific social and historical contexts.

The practical implication is that funders, policymakers, and researchers need to stop treating the question “how do we scale up Western psychiatric models in low-income countries?” as the primary question of global mental health. The primary question should be: “How do we build mental health systems that are meaningful, accessible, and effective for the specific communities they serve?” Sometimes the answer will involve biomedical psychiatry. Often it will involve traditional healers, community volunteers, religious leaders, and social interventions that address the structural roots of distress. Almost always it will require local leadership, genuine community co-design, and the humility to recognize that the Global North does not have a monopoly on wisdom about how human beings heal.

That shift from export to partnership, from uniformity to pluralism is the action point I hope this paper contributes to.

Interview With Shai Satran

The next few months we’ll be highlighting authors who have published in Culture, Medicine, and Psychiatry.

Shai Satran is a Postdoc at MIT in the program of Science, Technology, and Society. His research lies at the intersection of Anthropology, Psychology and Technology. His dissertation, Couch to Keyboard: Patients, Labor and Data in the Age of Psychotherapy Automation, is an ethnography of computerized therapy, its development and its dissemination in Israel’s public mental health system. He is also trained as a psychotherapist.

What is your article “From Craft to Labor: How Automation is Transforming the Practice of Psychotherapy about?

My article is about a novel form of therapist-assisted computerized therapy and how it is changing the ways in which therapists do psychotherapy. I argue that computerized therapy introduces what is a major change to how psychotherapy is conducted, namely, that it constitutes a shift in psychotherapy’s status as a profession, from craft to labor. I use these terms in the Marxist sense, but basically what I mean to say is that therapists today usually still retain a very high level of control over the content and form of their therapeutic work, and that this is now changing in significant ways. I detail how computerized psychotherapy’s ‘division of labor’ is minimizing the control and influence of the therapists conducting therapy, while introducing a new and  powerful level of management, and potentially degrading therapists’ status – but, and this is important, that it is also potentially of real value for patients.

Tell us a little bit about yourself and your research interests.

I was trained as a psychotherapist in Israel, and as a trainee I began practicing therapy. At a certain point I understood that I might find therapy more interesting to think about than to actually do, and decided to pursue a PhD through which I would be able to think deeply about issues related to psychotherapy. I think psychotherapy is fascinating and in my eyes still mysterious; how does it work? What is actually happening there? Beyond psychotherapy I have an interest in technology and its seemingly ever-growing role in our everyday life, dreams and fears.

What drew you to this project?

In one of the monthly seminars in the public clinic in which I was practicing, a psychology professor came to introduce a digital ‘gamified’ therapeutic app he developed as a supplement to face-to-face therapy. He presented the app, and a plethora of accompanying empirical evidence of its efficacy. After the lecture was over and the professor left, the head psychologist asked who would like to use the app with their patients. Over thirty therapists in the room, and not one raised their hand. I remember thinking “well, that’s interesting!”

What was one of the most interesting findings?

One thing that I found interesting, and this really came from ‘the field’ and not at all something that I expected to encounter, was the disparity in the experiences of computerized therapy between patients and therapists. While patients’ reactions were mixed of course, many of them describe the course of online therapy as a very positive, and beneficial, experience. Therapists, on the other hand, recognized the utility of this therapy but invariably described the experience as unfulfilling, and emphasized how they do not want to continue working as online therapists. I have come to realize that this gap between the experience of ‘service providers’ and ‘customers’ has become exceedingly common (e.g. Amaozn), and is in itself indicative of neoliberal trends and the professional shift I describe in the article.

What are you reading, listening to, and/or watching right now?

Unfortunately, I barely read for fun anymore! My next research project is a history of computer scientist Joseph Weizenbaum and his ELIZA computer program (1966) which famously impersonated a Rogerian (Carl Rogers’ client centered therapy) psychotherapist. So, I am reading through some of the seminal early texts of artificial intelligence; the things I imagine Weizenbaum must have been reading back then…

If there was one takeaway or action point you hope people will get from your work, what would it be?

That it would be a mistake to blindly vilify technology while romanticizing face to face interactions. I can understand, and even relate to, a certain disdain for the very idea of automating psychotherapy, but I think its worth remembering two things: First, there are real world constraints to providing quality care at scale and that different things work for different people. While many people may need a human relationship and a face to face encounter to experience positive change, others might actually do well with less than that. Second, not all in-person therapy is good therapy. Some of the patients I met during my research actually arrived at computerized therapy in order to avoid a face to face encounter with a therapist. It is painful but important to acknowledge that the very worst things that happen in therapy (malpractice, emotional abuse or sexual assault), even if they are rare, happen in face to face therapy.


Other places to connect:

2025 Early Career Development Award Winner

Congratulations to our 2025 Early Career Development Award winner, Harry Whittle, for his piece, Ronaldo on the Clapham Omnibus: Complex Recoveries in Complex Psychosis.

Harry is a psychiatrist and anthropologist in training. He is currently a doctoral researcher in the Department of Anthropology and Sociology at SOAS University of London, where he is part of the Centre for Anthropology and Mental Health Research in Action (CAMHRA). Harry’s research focuses on ideas of recovery, rehabilitation, and community in mental health and mental health services, particularly in relation to people living with more complex, severe, and enduring forms of psychosis.  

When asked about his article, Harry said:

In the article, I think critically about recovery in psychosis. I ask how it complicates our understanding of recovery if we consider the experiences of people with the most complex forms of psychosis, who have inadvertently been excluded from much debate on this topic. Drawing on six months of ethnography on an inpatient psychiatric rehabilitation unit, the article centres around a man I call Shepherd, whose journey to becoming a more confident, calmer, happier person was characterised by caution, masking, social withdrawal, and scepticism towards hope. These are embodied practices that seem incompatible with many portraits of recovery in the literature. Yet, here, they enabled—or even constituted—Shepherd’s recovery. The social complexities and ambivalences in his story reflect not only how complex recovery can be, but also how complex people’s relationships with mental health services can be. During his lengthy psychiatric admission, the coercive structures of the hospital were difficult to separate from the time, space, and relative safety they afforded Shepherd, which allowed him to figure out his recovery for himself. If we oversimplify recovery by missing people like Shepherd, we risk structurally undermining the interventions—like inpatient rehabilitation here—that may best support them to live well.

Congratulations, well earned!

Interview With Nora S. West

The next few months we’ll be highlighting authors who have published in Culture, Medicine, and Psychiatry.

Assistant Professor, University of California, San Francisco

I am a social scientist who uses qualitative and mixed methods within infectious disease screening, diagnostics, and therapeutics. My research interests focus on understanding mental health trajectories during diagnosis and treatment, the influence of mental health on engagement with infectious disease care cascades, and implementation science approaches for integrating mental health services into infectious disease care.

What is your article “Okweraliikirira and Okwenyamira: Idioms of Psychological Distress Among People Living with HIV in Rakai, Uganda” about?

This study explored how people living with HIV in rural Uganda understand and express psychological distress. Interviews were conducted with 42 people, including those living with HIV, healthcare workers, and community members. Two main local terms were used to describe mental distress: okweraliikirira (worry/apprehension) and okwenyamira (deep thoughts/many thoughts). These expressions of distress were specifically linked to HIV-related challenges like fear of death, stigma from family and community, disclosure concerns, and financial stress from managing HIV care. Both types of distress were said to worsen HIV medication adherence and could progress to more severe mental health problems if left unaddressed. Participants identified counseling and social support as key treatments. The study suggests that understanding culturally specific ways of expressing distress is important for healthcare provision. Using local terms rather than Western psychiatric labels like “depression” may help identify people who need psychosocial support and make screening culturally appropriate and effective.

Tell us a little bit about yourself and your research interests.

My research focuses on understanding the dynamics of mental health across care and treatment cascades for infectious diseases, primarily, TB and HIV.

What drew you to this project?

I worked on several studies that used mental health screeners among people living with infectious diseases, and from that work, I realized that the interpretation of the screeners and expressions of mental distress did not always map onto commonly used screeners.

What are you reading, listening to, and/or watching right now? (Doesn’t have to be anthropological!)

I have been reading Barbarian Days: A Surfing Life by William Finnegan and recently watched Downfall: The Case Against Boeing.

If there was one takeaway or action point you hope people will get from your work, what would it be?

Healthcare providers, mental health programs, and researchers should consider the relevance of incorporating culturally specific idioms of distress—like “okweraliikirira” (worry/apprehension) and “okwenyamira” (deep/many thoughts)—into their screening and treatment approaches rather than relying solely on Western diagnostic frameworks.

Other places to connect:

Website

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Interview With Agnes Ringer

The next few months we’ll be highlighting authors who have published in Culture, Medicine, and Psychiatry.

Editor, Hans Reitzels Forlag; Part-time Lecturer and Researcher, Roskilde University; Visiting Scholar, Vrije Universiteit Brussels

Agnes Ringer, is a clinical psychologist and interdisciplinary mental health researcher. She works as an editor in psychology and lectures part-time at Roskilde University. Her work centers on psychiatric practice, recovery, and the social dimensions of mental distress. Currently, she is a visiting scholar in Vrije Universiteit, Brussels.

What is your article Troublesome Bodies: How Bodies Come to Matter and Intrude in Eating Disorder Recovery about?

This article explores how the body becomes a site of tension and meaning in the process of recovery from eating disorders. Drawing on interviews with participants in a group therapy program, my co-authors, Mari Holen and Anne Mia Steno, and I show that recovery is not just about changing eating behavior or mindset—but about navigating how the body is viewed, judged, and experienced. We use theoretical perspectives from Sarah Ahmed and Analu Verbin to examine how bodies are shaped through social space and cultural paradoxes. The article introduces the concept of the ‘troublesome body’ to highlight how participants simultaneously seek and resist visibility, control and surrender,
and how their agency emerges through collective spaces like group therapy.

Tell us a little bit about yourself and your research interests.

I’m trained as a clinical psychologist and hold a PhD in interdisciplinary mental health.
My research focuses on psychiatric institutions, recovery, and how mental distress is
shaped by and expressed within social and institutional contexts. I’m especially interested
in how people respond to adversity—not as passive victims, but as meaning-making
agents who navigate their lives with dignity. My work draws on psychological,
sociological, and anthropological perspectives.

What drew you to this project?

The project grew out of my experience working in a clinic for eating disorders that used
group-based, narrative, and systemic therapy. I was struck by how transformative the
group process was, and how central the body became in participants’ stories. While my
co-authors and I set out to explore social aspects of recovery, we discovered that recovery
was deeply entangled with how participants experienced and navigated their bodies.

What are you reading, listening to, and/or watching right now? (Doesn’t have to be anthropological!)

Right now, I’m re-reading Agnes’s Jacket: A Psychologist’s Search for the Meanings of
Madness by Gail A. Hornstein. It’s a powerful exploration of first-person narratives in
mental health and what they can teach us about experience beyond diagnosis. I’m also
watching Hacks—a smart, sharp comedy that explores vulnerability, creativity, and
power dynamics.

If there was one takeaway or action point you hope people will get from your work, what would it be?

That recovery from eating disorders is not a linear, individual journey. It’s deeply social,
relational, and shaped by the environments we inhabit. We need spaces where people can
explore their paradoxes, be seen without judgment, and co-create new meanings together.

Other places to connect:

Website

Linkedin

Interview With Domonkos Sik 

The next few months we’ll be highlighting authors who have published in Culture, Medicine, and Psychiatry.

Associate Professor, Eötvös Loránd University, Budapest 

My research deals with various topics in critical theory including political culture and mental disorders in late modernity. My work has appeared in such venues as The Sociological Review, Theory, Culture & Society, European Journal of Social Theory, Thesis Eleven, Journal of Mental Health. Most recent books: Empty suffering (Routledge 2021) Salvaging modernity (Brill 2025).

What is your article Between Depression and Alienation: Burnout as a Translator Category for Critical Theories about?

The article explores the psychopathological and sociological discourses surrounding the contested notion of burnout, with the aim of reintroducing it as a ‘translator category’. Such concepts, which can translate between everyday language, medical language and critical language, are particularly important in cases which originate from both individual and social causes. Without these translator categories, biomedical and psychopathological interpretations veil the social components of suffering – therefore, inevitably mistreat it as an exclusively individual problem. Furthermore, attempts at social critique also remain inaccessible because they rely on their own set of diagnostic concepts (such as alienation), while lay actors interpret their suffering as an illness or mental disorder (such as depression). To avoid these dead ends, the article discusses how burnout as a translator category can link the discourses of alienation (as a cause of burnout) and depression (as a consequence of burnout) while remaining accessible as a lay category.

Tell us a little bit about yourself and your research interests.

I was trained as a sociologist and philosopher in post-socialist Hungary. Initially, my research focused on democratic transition, particularly its phenomenological features. Since 2010, however, my attention has shifted from the criteria of democratic culture to the personal consequences of failed democratization. This led me to explore the links between social suffering and mental health issues, a topic which has become my main area of expertise over the last decade.

What drew you to this project?

After exploring several clinical categories (e.g. depression, anxiety, addiction) from a critical theoretical-phenomenological perspective (see my book Empty Suffering) I became interested in a phenomenon located at the intersection of biomedical and lay discourses. This is how I found the topic of burnout, which is contested within the biomedical discourses, while being widely applied by the lay actors at the same time.

What are you reading, listening to, and/or watching right now? (Doesn’t have to be anthropological!)

I enjoy reading novels, viewing them not just as an excellent way to relax, but also as a constant source of inspiration for my social scientific work. As well as the better-known classics by authors such as Balzac and Dostoevsky, and contemporaries such as Ali Smith and Kazuo Ishiguro, I also enjoy the vivid Central European literary scene (authors such as Péter Nádas and Mircea Cărtărescu).

If there was one takeaway or action point you hope people will get from your work, what would it be?

Most mental health conditions are inextricably linked to social dysfunction and structural distortion. If we do not address the ‘social pathologies of contemporary civilization’ (that is also the name of a research network I am currently involved in: https://socialpath.org/), there is little hope of stopping the ‘epidemics’ of depression and burnout.

Other places to connect:

Website

Interview With Florin Cristea

The next few months we’ll be highlighting authors who have published in Culture, Medicine, and Psychiatry.

PhD candidate, Freie Universität Berlin

Florin Cristea is a PhD candidate in psychological and medical anthropology at the Freie Universität Berlin. His research focuses on understanding the moral world of people diagnosed with severe psychiatric disorders. In his work, he engaged with the social and clinical life worlds of people with a lived experience of psychiatric encounters in Romania, Tanzania, and Indonesia.

What is your article Navigating the Unknown: Mental Pain, Uncertainty, and Self-Isolation in Bali and Java about?

Suffering has long been a central theme in anthropology. Yet, despite growing interest in psychology and psychiatry, anthropological engagement with mental or emotional pain (as stand-alone concepts) has remained limited. In my article, based on fieldwork in Indonesia on severe psychiatric disorders, I tried to understand the impact of mental pain on the person experiencing it and their immediate environment. I first outlined the salient attributes of mental pain as they emerged during my conversations with patients and observations of their everyday lives. I then suggested that these attributes contributed to the uncertainties individuals faced as part of their experiences with severe psychiatric disorders. Finally, my main argument was that the interplay between mental pain and uncertainties informed certain illness behaviors, particularly tendencies toward self-isolation.     

Tell us a little bit about yourself and your research interests.

I am interested in the anthropology of mental health and illness, as well as in Global Health and Global Mental Health. I am fascinated by how different knowledge worlds come together and influence people’s understanding of what it means to be healthy, sick, and ultimately human. While my work has been strongly influenced by critical medical and psychological anthropology, I try to maintain an open engagement with the psy and biomedical sciences and seek venues of mutual understanding and collaboration.

What drew you to this project?

I initially was drawn to alternative understandings of the mind in Indonesia. However, mapping out these understandings proved far more complex than I had anticipated. Addressing mental pain was my way of making sense of the muddle that became my data.

What are you reading, listening to, and/or watching right now? (Doesn’t have to be anthropological!)

A friend recently recommended “Lightseekers” by Femi Kayode, and I am looking forward to reading it on my upcoming vacation. I am grateful to have time to enjoy something completely unrelated to work. 

If there was one takeaway or action point you hope people will get from your work, what would it be?

Isolation of people diagnosed with a severe psychiatric disorder is a fairly common problem, irrespective of where it occurs. It is important to note or to reiterate that isolation is not only the result of social attitudes toward mental illnesses, nor is it an individual issue. It is part and parcel of the intersubjective nature of the encounter between the social and the individual. We need to do better in understanding this relationship.  

Other places to connect:

Linkedin