Literature DB >> 26621264

Lay knowledge, social movements and the use of medicines: Personal reflections.

Nicky Britten1, Kath Maguire2.   

Abstract

This article consists of two personal reflections about the changing status of lay knowledge over the last 20 years. The first reflection is by Nicky Britten from the perspective of a sociologist working in medical schools whose interest in this topic was motivated by my own personal experience of health care and of teaching general practitioners. Starting with the problematic deficit model of 'ignorant patients', I trace the literature on patient-centredness, shared decision-making, lay knowledge, public involvement in research and social movements. Looking at medicines use in particular, I deplore the continued hegemony of the concept of compliance in the face of extensively documented problems with the licensing, regulation, prescribing and monitoring of medicines. I argue that lay knowledge is now taken more seriously, not so much because of advocacy by clinicians and academics, but because of social movements and social action. We may have moved from 'anecdotes' to 'lived experience' but there is still a way to go, particularly when it comes to medicines use. I end with a possible future scenario. The second reflection is by Kath Maguire and is a response from the perspective of someone who came to work in this field with the express purpose of improving engagement with lay knowledge. It questions my own 'layness' and explores the issues raised by Nicky Britten using the lens of lived experience. Finally, it questions the paradigm of social movements and highlights the importance of developing different ways of listening.
© The Author(s) 2015.

Entities:  

Keywords:  experiencing illness and narratives; illness behaviour; patient–physician relationship

Mesh:

Year:  2015        PMID: 26621264     DOI: 10.1177/1363459315619021

Source DB:  PubMed          Journal:  Health (London)        ISSN: 1363-4593


  8 in total

1.  "I know best:" women caring for kin with dementia.

Authors:  Ester Carolina Apesoa-Varano
Journal:  Soc Sci Med       Date:  2020-05-05       Impact factor: 4.634

2.  Understanding each other in the medical encounter: Exploring therapists' and patients' understanding of each other's experiential knowledge through the Imitation Game.

Authors:  Rik Wehrens; Bethany Hipple Walters
Journal:  Health (London)       Date:  2017-08-03

Review 3.  Bipolar patients and creative online practices: Sharing experiences of controversial treatments.

Authors:  Claudia Egher
Journal:  Health (London)       Date:  2019-03-28

4.  Public involvement in research about environmental change and health: A case study.

Authors:  Kath Maguire; Ruth Garside; Jo Poland; Lora E Fleming; Ian Alcock; Tim Taylor; Helen Macintyre; Gianni Lo Iacono; Andrew Green; Benedict W Wheeler
Journal:  Health (London)       Date:  2019-03

5.  Experience as knowledge: Disability, distillation and (reprogenetic) decision-making.

Authors:  Felicity K Boardman
Journal:  Soc Sci Med       Date:  2017-09-08       Impact factor: 4.634

6.  Patients' and clinicians' perceptions of oral anticoagulants in atrial fibrillation: a systematic narrative review and meta-analysis.

Authors:  Yeyenta Mina Osasu; Richard Cooper; Caroline Mitchell
Journal:  BMC Fam Pract       Date:  2021-12-22       Impact factor: 2.497

7.  Revisiting Candidacy: What Might It Offer Cancer Prevention?

Authors:  Samantha Batchelor; Emma R Miller; Belinda Lunnay; Sara Macdonald; Paul R Ward
Journal:  Int J Environ Res Public Health       Date:  2021-09-27       Impact factor: 3.390

8.  Epistemic solidarity in medicine and healthcare.

Authors:  Mirjam Pot
Journal:  Med Health Care Philos       Date:  2022-08-31
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.