All Stories

  1. Why time matters at work
  2. Quietism is a new form of gender discrimination used to silence women
  3. A Racialized Capitalism Perspective on the Work and Employment of Black and Minoritized Ethnic Workers Living With Sickle Cell Disorder
  4. Editorial: Voices from the frontline: the lived experiences of healthcare professionals in the workplace
  5. Is the workplace about to get better or worse for disabled people in the United Kingdom?
  6. Editorial: Intersections of ageing and disability during the COVID-19 pandemic
  7. Bridging the Gap
  8. Sickle Cell Disease and Its Psychosocial Burdens in Africa
  9. Social Determinants of Severity in Sickle Cell Disease
  10. The Critical Importance of Global Collaboration in SCD Advocacy and Management
  11. The indignities of shielding during the COVID-19 pandemic for people with sickle cell disorders: an interpretative phenomenological analysis
  12. Philosophical and practical challenges of Ubuntu
  13. Representing disabling experiences: Rethinking quality of life when evaluating public health interventions
  14. Social Science Research and Sickle Cell Disorders
  15. Social Science Research and Sickle Cell Disorders
  16. Black sickle cell patients’ lives matter: healthcare, long-term shielding and psychological distress during a racialised pandemic in England – a mixed-methods study
  17. Repercussions of overturning Roe v. Wade for women across systems and beyond borders
  18. “I want to become someone!” gender, reproduction and the moral career of motherhood for women with sickle cell disorders
  19. Let's Get Back to Normal? COVID-19 and the Logic of Cure
  20. An African Path to Disability Justice: Community, Relationships and Obligations
  21. 3. An African Ethics of Social Well-Being: Understanding Disability and Public Health
  22. "Let's get back to normal!" COVID-19 and the logic of cure
  23. An African Ethics of Social Well-Being: Understanding Disability and Public Health
  24. On the possibility of a disabled life in capitalist ruins: Black workers with sickle cell disorder in England
  25. Who Gets Cured? COVID-19 and Developing a Critical Medical Sociology and Anthropology of Cure
  26. ‘They Can Replace You at Any Time!’: (In)Visible Hyper-Ableism, Employment and Sickle Cell Disorders in England
  27. Biosocial Model of Disability
  28. Competing ethics in a pilot strategy to implement parasitology training and research in post-Ebola Sierra Leone
  29. Intersectionality and employment in the United Kingdom: Where are all the Black disabled people?
  30. “You have to find a caring man, like your father!” gendering sickle cell and refashioning women's moral boundaries in Sierra Leone
  31. Time to apply a social determinants of health lens to addressing sickle cell disorders in sub-Saharan Africa
  32. Biosocial Model of Disability
  33. Incidental Findings of Sickle Cell Trait From an Everyday Diabetes Test: Should General Health Care Providers and Testing Centers Report, Retest, or Refer?
  34. The Routledge Handbook of Disability Activism
  35. Disability Futures
  36. Introducing Disability Activism
  37. Rights to social determinants of flourishing? A paradigm for disability and public health research and policy
  38. Do disabled people need a stronger social model: a social model of human rights?
  39. Ethnicity, disability and chronic illness
  40. Ethnicity, disability and chronic illness
  41. Ethical (dis)enchantment, afflictive kinship, and Ebola exceptionalism
  42. Cash not care: the planned demolition of the UK welfare state
  43. Public health, research and rights: the perspectives of deliberation panels with politically and socially active disabled people
  44. Practices and discourses of ubuntu: Implications for an African model of disability?
  45. Practices and discourses of ubuntu: Implications for an African model of disability?
  46. Emancipatory Engagement and Co-Production: Disability Research for Activism
  47. Resignifying the sickle cell gene: Narratives of genetic risk, impairment and repair
  48. Implications for public health research of models and theories of disability: a scoping study and evidence synthesis
  49. SITES OF EXCEPTION. HIV Exceptionalism: Development through Disease in Sierra Leone. By Adia Benton. Minneapolis: University of Minnesota Press, 2015. Pp. xii + 176. $79, hardback (ISBN 9780816692422); $22.50, paperback (ISBN 9780816692439).
  50. The New Humanitarianism
  51. Neoliberal policy, chronic corruption and disablement: biosecurity, biosocial risks and the creation of ‘Ebola survivors’?
  52. War and Embodied Memory
  53. Disabled People in Conflicts and Wars
  54. Book Review of Disability Research Today: International Perspectives
  55. Radicalising Disability
  56. ‘Who's the guy in the room?’ Involving fathers in antenatal care screening for sickle cell disorders
  57. Fathers and Sickle Cell Screening
  58. Gun violence
  59. Native American communities on health and disability: borderland dialogues
  60. Mixed-Methods Approaches in a Post-Conflict Ethnographic Case Study with War-Wounded People
  61. Limitations of Individualistic Peacebuilding in Postwar Sierra Leone
  62. A Comparative Analysis: Everyday Experiences of Disability in Sierra Leone
  63. Paying for stories of impairment – parasitic or ethical? Reflections undertaking anthropological research in post-conflict Sierra Leone
  64. Review of Barron and Ncube, Poverty and Disability
  65. Emotion and Embodiment in Sierra Leone
  66. Coming to terms with inequality and exploitation in an African state: researching disability in Sierra Leone
  67. Book reviews
  68. Practices of responsibility and nurses during the euthanasia programs of Nazi Germany: A discussion paper
  69. Nursing, obedience, and complicity with eugenics: a contextual interpretation of nursing morality at the turn of the twentieth century
  70. The complexity of nurses' attitudes toward euthanasia: a review of the literature