All Stories

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