All Stories

  1. Psychiatrization, assertions of epistemic justice, and the question of agency
  2. De-psychiatrizing our own research work
  3. Leerstellen der gegenwärtigen Psychiatriekritik
  4. Politicising crisis support: learning from autonomous self-organising in Bochum, Germany
  5. The Routledge International Handbook of Mad Studies
  6. Afterword
  7. The international foundations of Mad Studies
  8. Patient and public involvement in research
  9. Experiential knowledge in mental health policy and legislation: can we ever change the agenda?
  10. Commentary on: Happell, B. & Scholz, B (2018). Doing what we can, but knowing our place: Being an ally to promote consumer leadership in mental health. International Journal of Mental Health Nursing , 27, 440-447
  11. Recovery, mental health and inequality. Chinese ethnic minorities as mental health service users
  12. Scenarios for the future of mental health care: whose interests, whose perspectives, whose future?
  13. Supporting the sustainability of Mad Studies and preventing its co-option
  14. In dialogue with conventional narrative research in psychiatry and mental health
  15. Establishing first-person knowledge of madness: Must This Undertaking Elide our Differences?
  16. Psychiatry disrupted: theorizing resistance and crafting the (r)evolution
  17. Die epistemische Dominanz unterbrechen – Anforderungen an die Forschung
  18. Between exclusion and colonisation: seeking a place for mad people’s knowledge in academia
  19. Mental health service users in research: critical sociological perspectives
  20. “But what if nobody's going to sit down and have a real conversation with you?” Service user/survivor perspectives on human rights
  21. Taking part in a pharmacogenetic clinical trial: assessment of trial participants understanding of information disclosed during the informed consent process
  22. Development of the ITHACA Toolkit for monitoring human rights and general health care in psychiatric and social care institutions
  23. Resisting Variables - Service User/Survivor Perspectives on Researching Coercion
  24. Roles
  25. The importance of user controlled research on coercion
  26. What we talk about when we talk about disability: