Nicole Cort
Biographic Data
| ID | 3603796 |
|---|---|
| NAME | Nicole Cort |
| GIVEN NAMES | Nicole |
| FAMILY NAME | Cort |
| SIGNATURE | CORT N |
| AFFILIATIONS | The University of Sydney |
| ORCID | 0000-0001-8434-5994 |
| VERIFIED | Yes |
| TOTAL WORKS | 84 |
| TOTAL CITATIONS | 613 |
| AUTHOR COUNT | 84 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2004 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 14 |
Rethinking fussiness in commercial food contexts
So-called ‘fussy’ or ‘picky’ eating has been construed as a problem of parenting feeding practices and children’s defiant eating behaviours. However, this ‘fussiness’ about food unfolds in a food environment rife with misleading marketing messages, conflicting information, and the widespread availability of ultra-processed food (UPF). Where fussiness leads to dietary patterns high in UPF, it can have significant implications for a child’s life-lo…
Caring infrastructures for sexual health and the implications of antibiotic-resistant STIs
Infrastructures fundamentally shape sexual health, but their gaps and failings often only come into view during moments of crisis. Antimicrobial resistance (AMR) is a looming microbiological and global societal crisis, and one that is posing increasing challenges and risks for medical practice and public health alike. In sexual health, concerns have been raised about growing resistance in Neisseria gonorrhoeae and the less well-known Mycoplasma g…
Unpacking the Assumptions, Oversights and Consequences that Surround Young People’s Difficulties in Accessing Chronic Illness Diagnosis and Care
Young people living with chronic illness navigate a series of age-specific difficulties that emerge from the way in which both youth and chronic illness are constructed in social and healthcare imaginaries. In this article we draw on 33 interviews with young adults (aged 19–29 years) living in Australia to examine the ways in which age is a factor that shapes the barriers and biases young people face when seeking therapeutic interventions for ill…
The school lunchbox as a social problem
School lunchboxes contain much more than just food. Maternal and paternal moralities, socioeconomic pressures, and the character of contemporary food systems can all be found within them. Lunchboxes, in turn, are microcosms of food system shifts, including the proliferation of highly-profitable, strategically-engineered ultra-processed foods. These commodities, often representing between 40% and 80% of energy intake depending on contexts, are hav…
Ensuring Responsible Nanotechnology Innovation
The challenge of considering the ethical, environmental, economic, social, legal and cultural (E 3 LSC) dimensions of nanotechnology innovation is of enduring and increasing importance for societies worldwide. This is made more pressing due to rising public interest in the realms of AI and quantum technology. Drawing on an interdisciplinary collaboration between nanotechnology and social science researchers, this paper discusses how E 3 LSC dimen…
Future/tense: A sociology of temporal dis/order
The last few years of pandemic living have highlighted various temporal tensions that characterise our individual and collective futures. In some ways, the scale of temporal disruption caused by the pandemic could be considered unprecedented. But in other ways, the temporal tensions that underpin social life are long-standing, even routine. In this special issue, ‘Future/Tense: A Sociology of Temporal Dis/Order’, we take the intensification of te…
Growing up, ill: The challenges of youth for young people living with chronic illness
The (Anti)Microbial Gaze: Surveillance Meets Resistance
Antimicrobial resistance (AMR) is a rapidly escalating global health threat, known increasingly through different forms of monitoring. Surveillance, both of resistant organisms and of the antimicrobial prescribing practices that contribute to their proliferation, has increased dramatically over the last decade. So too have audits, which are routinely deployed to evaluate, and ensure accountability for, the alignment of local prescribing practices…
It's very hard to have a future when you can't travel: Meaning, mobility and mortality after a cancer diagnosis
Being diagnosed with a life-limiting illness entails a fundamental reshaping of one's relationship with the future. From 'bucket lists' of destinations and experiences to 'flights of hope' for experimental or specialised medical care, diagnoses of serious illness are deeply entwined with travel in Australian cultural narratives. In this paper, we draw on a thematic analysis of interviews with cancer patients and their carers to ask what meanings …
Dying as a Collective Encounter: Relationality and Affect at the End of Life
The end of life is replete with relational complexities. Yet, despite the work of humanities and social science scholars in the field of death and dying, our final days and weeks are still often framed through a highly individualistic lens. As a result, the collective encounters of dying can become sidelined within the management of an individual's embodied journey. This, in some cases, has the effect of obscuring the presence and power of collec…
Navigating the Limits of Diagnosis: Young Adults' Experiences of Chronic Living
Young adults living with chronic illness often experience considerable uncertainty across the emotional, cultural and medical spheres of their everyday lives. The process of seeking, receiving and reckoning with a diagnosis has frequently been an in‐road for qualitative examinations of these experiences. As a result, the biomedical diagnosis has often taken centre stage in research concerning how uncertainty is managed and/or more stability is fo…
Conceptualising care: Critical perspectives on informal care and inequality
Informal care occupies a paradoxical place in contemporary societies. It is at once reified as an inherent social good, and minimised, devalued, and pushed to the margins. The current ‘care crisis’ is bringing these tensions into sharp relief, fuelling renewed interest in care and its absences across a wide range of disciplines. In this article, we present an overview of five key literatures for comprehending informal care, with a focus on issues…
The administration of harm: From unintended consequences to harm by design
Harm is a recurring theme in the social sciences. Scholars in a range of empirical areas have documented the deleterious outcomes that at times emerge from social structures, institutions and systems of governance. Yet these harms have often been presented under the rubric of ‘unintended consequences’. The outcomes of systems are designed to appear devoid of intentionality, in motion without any clear agency involved, and are thus particularly ad…
Entanglements of affect, space, and evidence in pandemic healthcare: An analysis of Australian healthcare workers’ experiences of Covid-19
Reciprocity, Autonomy, and Vulnerability in Men's Experiences of Informal Cancer Care
Men are increasingly participating, and acknowledging their roles, as informal carers. Yet, there has been comparatively little exploration of their experiences therein, especially within the context of cancer care. Here, drawing on semi-structured qualitative interviews with 16 Australian male carers for a relative with cancer, and using constructivist grounded theory, we explore their experiences of informal caring. Our analysis highlights a se…
Help-seeking prior to male suicide: Bereaved men perspectives
What lies beneath? Experiencing emotions and caring in oncology
Medical encounters - while often viewed as centred on conveying clinical knowledge - are also sites of emotion and for exerting emotional labour by healthcare professionals. The temptation to view these encounters as largely 'technical' - an exchange of knowledge or information - can marginalise the complex emotions often experienced by healthcare professionals, and negates the critical work done in these encounters. Drawing on in-depth interview…
Is Depression Associated with Unhealthy Behaviors among Middle-Aged and Older Women with Hypertension or Heart Disease
Unravelling subjectivity, embodied experience and (taking) psychotropic medication
This paper explores how distinctions between 'intended' and 'side' effects are troubled in personal narratives of taking psychotropic medications. Grounded in interviews with 29 participants diagnosed with mental illness in Victoria, Australia between February and December 2014, we consider how people interpret pharmaceutical compounds beyond their desired or intended effects, and how such effects shape and transform subjectivity and their relati…
Unpacking Social Isolation in Men's Suicidality
Social isolation has featured as a significant and oftentimes all-encompassing risk factor for male suicide, yet, as an explanatory mechanism, it has not been unpacked in terms of what it constitutes in everyday life. The current photovoice study explores the various dimensions of the lived experience of social isolation, as embedded in accounts of suicidality drawn from 35 Canadian men. Study participants narrated the following factors as underp…
I Never Saw a Future: Childhood Trauma and Suicidality Among Sexual Minority Women
While a significant health concern for sexual minority women, there is little qualitative research investigating their experiences of childhood trauma and suicidality. In this study, we used photovoice methods and an intersectionality framework. Drawing on qualitative interviews, we inductively derived three themes (a) Traumatized and discredited, (b) Cascading marginality, estrangement, and suicidality, (c) Reconstruction and reclaiming resilien…
Suicide Prevention From the Perspectives of Gay, Bisexual, and Two-Spirit Men
Although gay, bisexual, and two-spirit men (GBTSM) experience high rates of suicidality, there have been few empirical studies of prevention initiatives and policies that could address or reverse this major social problem. This article reports on a photovoice study of 29 GBTSM who had a history of suicidality or lost a fellow GBTSM to suicide. We focused our analysis on participants' perspectives on suicide prevention. Participants described four…
Authenticity, ambivalence and recognition in caring at the end of life and beyond
In one's own time: Contesting the temporality and linearity of bereavement
This article explores the experience and meaning of time from the perspective of caregivers who have recently been bereaved following the death of a family member. The study is situated within the broader cultural tendency to understand bereavement within the logic of stages, including the perception of bereavement as a somewhat predictable and certainly time-delimited ascent from a nadir in death to a 'new normal' once loss is accepted. Drawing …
Depression at work, authenticity in question: Experiencing, concealing and revealing
Australia and the United Kingdom have introduced policies to protect employees who experience mental illness, including depression. However, a better understanding of the experiential issues workers face (e.g. sense of moral failure) is needed for the provision of appropriate and beneficial support. We analysed 73 interviews from the United Kingdom and Australia where narratives of depression and work intersected. Participants encountered difficu…
Virtually He@lthy: The Impact of Internet Use on Disease Experience and the Doctor-Patient Relationship
In the current study, the author explores the complex effects and contradictory roles of the Internet as a source of empowerment and control, and as a site of 'risk management.' Drawing on a study of the Internet usage of Australian men with prostate cancer, the author investigates how access to information and online support affects men's experiences of disease and, in particular, the possible implications of Internet-informed patients for the d…
Cultures of resistance? A Bourdieusian analysis of doctors' antibiotic prescribing
The role of gender, environment and Individual biography in shaping qualitative interview data
Reflexivity is a key aspect of qualitative research. Considerable attention has been given to the ways in which gender mediates the production and analysis of qualitative data; however, much of this has been focused on qualitative interviews with women and the influence of the interviewer’s gender in this specific context. Very little work has been done on comparing different interviewer–interviewee contexts such as male‐to‐female, male‐to‐male o…
The inequalities of medical pluralism: Hierarchies of health, the politics of tradition and the economies of care in Indian oncology
Photovoice Ethics: Critical Reflections From Men's Mental Health Research
As photovoice continues to grow as a method for researching health and illness, there is a need for rigorous discussions about ethical considerations. In this article, we discuss three key ethical issues arising from a recent photovoice study investigating men's depression and suicide. The first issue, indelible images, details the complexity of consent and copyright when participant-produced photographs are shown at exhibitions and online where …
Medical specialists' accounts of the impact of the Internet on the doctor/patient relationship
In the context of health service delivery, deprofessionalization denotes a trend towards a demystification of medical expertise and increasing lay scepticism about health professionals, suggesting a decline in the power and status of the medical profession. This process has been linked to increasing consumerism, the rise of complementary medicine and the emergence of the Internet. Drawing on data from in-depth interviews with prostate cancer spec…
The eMale: Prostate cancer, masculinity and online support as a challenge to medical expertise
This article argues that experiences of, and attitudes towards, online communities are deeply embedded in understandings of masculinity, the perceived character of the Internet, and changes in the roles of the patient and the expert within decision-making processes. Drawing on the accounts of a group of Australian men with prostate cancer and prostate cancer specialists, this qualitative study explores experiences of online support groups. Result…
Masculinity, moralities and being cared for: An exploration of experiences of living and dying in a hospice
Evidence-based healthcare in practice: A study of clinician resistance, professional de-skilling, and inter-specialty differentiation in oncology
Exploring the Temporal Dimension in Cancer Patients' Experiences of Nonbiomedical Therapeutics
To date, research on complementary and alternative medicine (CAM) use by cancer patients has tended to provide a "snapshot" of experience, with little attention given to the evolution of experience over time. Drawing on data from solicited diaries, this article examines individual cancer patients' temporal experiences of CAM. Our findings suggest that experiences of CAM are variable over time and space, and furthermore, that the everyday act of "…
Intuition, Subjectivity, and Le Bricoleur: Cancer Patients' Accounts of Negotiating a Plurality of Therapeutic Options
Cancer patients are now combining complementary and alternative medicine (CAM) with biomedical cancer treatments, reflecting an increasingly pluralistic health care environment. However, there has been little research done on the ways in which cancer patients juggle multiplicity in claims to expertise, models of disease, and therapeutic practice. Drawing on the accounts of cancer patients who use CAM, in this article I develop a conceptualization…
The administration of harm: From unintended consequences to harm by design
Harm is a recurring theme in the social sciences. Scholars in a range of empirical areas have documented the deleterious outcomes that at times emerge from social structures, institutions and systems of governance. Yet these harms have often been presented under the rubric of ‘unintended consequences’. The outcomes of systems are designed to appear devoid of intentionality, in motion without any clear agency involved, and are thus particularly ad…
The art of letting go: Referral to palliative care and its discontents
The role of the Internet in cancer patients' engagement with complementary and alternative treatments
This article draws on a study of 80 National Health Service cancer patients and their experiences of using the Internet within disease and treatment processes. It focuses on the role the Internet plays in the context of potential or actual engagement with complementary and alternative medicine (CAM). The results depart from previous conceptualizations of the Internet as a major source of CAM knowledge, and second, as a major pathway to patient CA…
On the meanings and experiences of living and dying in an Australian hospice
Drawing on qualitative interviews with patients near death, in this article we explore people's experiences of living and dying in a hospice in-patient unit. The results illustrate the tensions and complexities of entering into the hospice environment and how its character (i.e. people, interactions and spaces) shapes experiences near death.The results illustrate the hospice in-patient unit as playing a vitally important role in supporting the en…
The Troubles of Telling: Managing Communication About the End of Life
Communication about palliative care represents one of the most difficult interpersonal aspects of medicine. Delivering the "terminal" diagnosis has traditionally been the focus of research, yet transitions to specialist palliative care are equally critical clinical moments. Here we focus on 20 medical specialists' strategies for engaging patients around referral to specialist palliative care. Our aim was to develop an understanding of the logics …
The Liminal and the Parallax: Living and Dying at the End of Life
Transitions to palliative care can involve a shift in philosophy from life-prolonging to life-enhancing care. People living with a life-limiting illness will often receive palliative care through specialist outpatient clinics, while also being cared for by another medical specialty. Experiences of this point of care have been described as being liminal in character, that is, somewhere between living and dying. Drawing on experiences of illness an…
The social dynamics of antibiotic use in an Australian hospital
Misuse of antibiotics in hospitals in Australia and internationally is common. The combination of multi-resistant organisms and continued misuse of antibiotics is contributing to a predicted 'antimicrobial perfect storm' in the coming decades. Attempts to influence doctors' use of antibiotics have seen limited success internationally, yet few studies have explored the potential social factors driving current practices within hospitals and the int…
Negotiating Futility, Managing Emotions: Nursing the Transition to Palliative Care
Nurses play a pivotal role in caring for patients during the transition from life-prolonging care to palliative care. This is an area of nursing prone to emotional difficulty, interpersonal complexity, and interprofessional conflict. It is situated within complex social dynamics, including those related to establishing and accepting futility and reconciling the desire to maintain hope. Here, drawing on interviews with 20 Australian nurses, we unp…
I'd forgotten about me in all of this: Discourses of self-healing, positivity and vulnerability in cancer patients' experiences of complementary and alternative medicine
Drawing on in-depth interviews with Australian cancer patients, this article examines their experiences of utilizing complementary and alternative medicine (CAM) within disease and treatment processes. Results illustrate the complex and often contradictory roles played by CAM within patients' therapeutic trajectories. On the one hand, their accounts illustrate the liberating and positive impacts of CAM engagement, including perceived increases in…
Oncologists' and specialist cancer nurses' approaches to complementary and alternative medicine and their impact on patient action
In one's own time: Contesting the temporality and linearity of bereavement
This article explores the experience and meaning of time from the perspective of caregivers who have recently been bereaved following the death of a family member. The study is situated within the broader cultural tendency to understand bereavement within the logic of stages, including the perception of bereavement as a somewhat predictable and certainly time-delimited ascent from a nadir in death to a 'new normal' once loss is accepted. Drawing …
The symbolic affordances of a video-mediated gaze in emergency psychiatry
The path of least resistance? Jurisdictions, responsibility and professional asymmetries in pharmacists' accounts of antibiotic decisions in hospitals
My dirty little habit: Patient constructions of antidepressant use and the 'crisis' of legitimacy
State of the Art: A Decade of Health Sociology in Review
This paper reports on a review of health sociology in Australia from 1990 till present. The authors searched all the major databases for health social sciences including Medline, CINAHL, Sociological Abstracts and Australian Medical Index. Methodological difficulties in capturing all such work are outlined first. Examination of the citations revealed a significant increase in research and commentary in the discipline, and a continued (since the l…
Virtually He@lthy: The Impact of Internet Use on Disease Experience and the Doctor-Patient Relationship
In the current study, the author explores the complex effects and contradictory roles of the Internet as a source of empowerment and control, and as a site of 'risk management.' Drawing on a study of the Internet usage of Australian men with prostate cancer, the author investigates how access to information and online support affects men's experiences of disease and, in particular, the possible implications of Internet-informed patients for the d…
Medical specialists' accounts of the impact of the Internet on the doctor/patient relationship
In the context of health service delivery, deprofessionalization denotes a trend towards a demystification of medical expertise and increasing lay scepticism about health professionals, suggesting a decline in the power and status of the medical profession. This process has been linked to increasing consumerism, the rise of complementary medicine and the emergence of the Internet. Drawing on data from in-depth interviews with prostate cancer spec…
The eMale: Prostate cancer, masculinity and online support as a challenge to medical expertise
This article argues that experiences of, and attitudes towards, online communities are deeply embedded in understandings of masculinity, the perceived character of the Internet, and changes in the roles of the patient and the expert within decision-making processes. Drawing on the accounts of a group of Australian men with prostate cancer and prostate cancer specialists, this qualitative study explores experiences of online support groups. Result…
Reflections on the centrality of power in medical sociology: An empirical test and theoretical elaboration
This paper explores the contemporary relevance of sociological theorisations centred on medical power, including the medical dominance and deprofessionalisation theses. To achieve this it examines two issues that have been tentatively linked to the relative decline of the power and autonomy of biomedicine - complementary and alternative medicine (CAM) and the Internet-informed patient. Drawing on these two different but interconnected social phen…
Cancer Patients' Negotiation of Therapeutic Options in Pakistan
Cancer is the second leading cause of death in Pakistan. There is increasing evidence that patients are using a range of (biomedical and nonbiomedical) therapeutic options for cancer treatment. To date there has been no sociologically informed research into the engagement of cancer patients in Pakistan with available modalities. In this article, the authors present findings from the first such study. They purposively sampled 46 cancer patients fr…
Oncologists' and specialist cancer nurses' approaches to complementary and alternative medicine and their impact on patient action
The role of gender, environment and Individual biography in shaping qualitative interview data
Reflexivity is a key aspect of qualitative research. Considerable attention has been given to the ways in which gender mediates the production and analysis of qualitative data; however, much of this has been focused on qualitative interviews with women and the influence of the interviewer’s gender in this specific context. Very little work has been done on comparing different interviewer–interviewee contexts such as male‐to‐female, male‐to‐male o…
Exploring the Temporal Dimension in Cancer Patients' Experiences of Nonbiomedical Therapeutics
To date, research on complementary and alternative medicine (CAM) use by cancer patients has tended to provide a "snapshot" of experience, with little attention given to the evolution of experience over time. Drawing on data from solicited diaries, this article examines individual cancer patients' temporal experiences of CAM. Our findings suggest that experiences of CAM are variable over time and space, and furthermore, that the everyday act of "…
The role of the Internet in cancer patients' engagement with complementary and alternative treatments
This article draws on a study of 80 National Health Service cancer patients and their experiences of using the Internet within disease and treatment processes. It focuses on the role the Internet plays in the context of potential or actual engagement with complementary and alternative medicine (CAM). The results depart from previous conceptualizations of the Internet as a major source of CAM knowledge, and second, as a major pathway to patient CA…
The problematic nature of conflating use and advocacy in CAM integration: Complexity and differentiation in UK cancer patients' views
The integration of complementary and alternative medicine into cancer care is widely debated. Advocates of integration frequently cite the popularity of such therapies amongst patients in support of their case. However, little specific empirical attention has been given to how integration is actually regarded by these patients. Based on semi structured interviews with 80 cancer patients in the UK, this article examines the assumption of a link be…
Archiving Qualitative Data in Australia: An Introduction
The prospect of the digital archiving of qualitative data for re‐use and analysis by other researchers is now a distinct reality in Australia following the development of similar facilities in the UK, the US and Finland. While these archives are now well‐established and have become reasonably well‐accepted among the scholarly community, their development has not been uncontroversial and has stimulated much debate about the desirability and feasib…
Intuition, Subjectivity, and Le Bricoleur: Cancer Patients' Accounts of Negotiating a Plurality of Therapeutic Options
Cancer patients are now combining complementary and alternative medicine (CAM) with biomedical cancer treatments, reflecting an increasingly pluralistic health care environment. However, there has been little research done on the ways in which cancer patients juggle multiplicity in claims to expertise, models of disease, and therapeutic practice. Drawing on the accounts of cancer patients who use CAM, in this article I develop a conceptualization…
The inequalities of medical pluralism: Hierarchies of health, the politics of tradition and the economies of care in Indian oncology
Evidence-based healthcare in practice: A study of clinician resistance, professional de-skilling, and inter-specialty differentiation in oncology
Oncology clinicians' accounts of discussing complementary and alternative medicine with their patients
The profile of complementary and alternative medicine (CAM) has risen dramatically over recent years, with cancer patients representing some of the highest users of any patient group. This article reports the results from a series of in-depth interviews with oncology consultants and oncology nurses in two hospitals in Australia. Analysis identifies a range of self-reported approaches with which oncology clinicians discuss CAM, highlighting the po…
I'd forgotten about me in all of this: Discourses of self-healing, positivity and vulnerability in cancer patients' experiences of complementary and alternative medicine
Drawing on in-depth interviews with Australian cancer patients, this article examines their experiences of utilizing complementary and alternative medicine (CAM) within disease and treatment processes. Results illustrate the complex and often contradictory roles played by CAM within patients' therapeutic trajectories. On the one hand, their accounts illustrate the liberating and positive impacts of CAM engagement, including perceived increases in…
The Prevalence and Politics of HIV/Aids in Zimbabwe: Examining the Ideological, Political and Historical Factors Behind the ‘Decline
The reported reduction in the prevalence level of the Human Immunodeficiency Virus (HIV) in Zimbabwe has been represented as one of the most significant and rapid declines within any population since the epidemic emerged as a public health issue. This paper explains how this development has been reported, challenged and eventually owned by many of the diverse stakeholders who constitute Zimbabwe's overall AIDS response. The Zimbabwean government …
Masculinity, moralities and being cared for: An exploration of experiences of living and dying in a hospice
The Reconfiguration of Expertise in Oncology: The Practice of Prediction and Articulation of Indeterminacy in Medical Consultations
Evidence-based medicine has enhanced the predictive capacity of biomedicine in population terms, but it has also introduced new challenges for patient care and biomedical expertise. In this article we examine the negotiation of prediction and indeterminacy by oncology clinicians, exploring the ways in which they report delivering prognosis and engaging with indeterminacy in conversation with their patients. We examine oncologists' strategies for …
Evidence produced by qualitative investigations on type 2 diabetes: A review of the literature
Type 2 diabetes has a major impact on patients lives and the healthcare network. Given the growth in qualitative information on diabetes, it becomes important to systematize this knowledge. A meta-study on diabetes was conducted through analysis on 42 articles that were made in journals at the periodicals portal of the Coordination Office for Advancement of Higher-level Personnel (Capes). We found that the studies reviewed had a good theoretical …
On the meanings and experiences of living and dying in an Australian hospice
Drawing on qualitative interviews with patients near death, in this article we explore people's experiences of living and dying in a hospice in-patient unit. The results illustrate the tensions and complexities of entering into the hospice environment and how its character (i.e. people, interactions and spaces) shapes experiences near death.The results illustrate the hospice in-patient unit as playing a vitally important role in supporting the en…
The art of letting go: Referral to palliative care and its discontents
On Euthanasia, Resistance, and Redemption: The Moralities and Politics of a Hospice
Euthanasia/assisted dying, the desire to hasten death, and religious supportive care at the end of life are controversial issues that have been heavily debated within the academic and medical communities. Little research has been done on hospice patients' views, despite hospices being political spaces, espousing a range of perspectives on assisted dying, religiosity, and "good deaths." In this article I document the presence, articulation, and si…
The rise of cancer in urban India: Cultural understandings, structural inequalities and the emergence of the clinic
Cancer services in India have evolved and expanded significantly in recent years, with a surge in the availability of biomedical oncological treatment facilities for certain cohorts of the Indian population in urban areas. Despite significant and sustained economic development in many areas of India, major issues persist in the delivery of cancer care, even in the context of relatively prosperous urban populations. This article explores the dilem…
Sociology (53 works) · Psychology (51 works) · Medicine (48 works) · Political science (40 works) · Social Psychology (31 works) · Social science (23 works) · Law (21 works) · Qualitative research (21 works) · Epistemology (19 works) · Nursing (18 works)