A discourse analytic study of ME/CFS (Chronic Fatigue Syndrome) sufferers' experiences of interactions with doctors
Datos Bibliográficos
| ID | 4228950 |
|---|---|
| Autores | Jennie Guise (University of Abertay Dundee, UK,), Chris Mcvittie (0000-0003-0657-7524, Queen Margaret University), Andy Mckinlay (University of Edinburgh) |
| Año | 2010 |
| Volumen | 15 |
| Número | 3 |
| Páginas | 426-435 |
| Fecha de publicación | 2010-04-01 |
| Peer Reviewed | Sí |
| Open Access | Sí |
| Tipo | ARTICLE |
| Revista | Journal of Health Psychology (JOURNAL) |
| Identificadores de la revista | ISSN: 1359-1053 • E-ISSN: 1461-7277 |
| Editorial | SAGE Publications Inc (PUBLISHER) |
| DOI | 10.1177/1359105309350515 |
| PMID | 20348363 |
| OpenAlex | W2136031857 |
| Idioma | EN |
| Citas recibidas | 13 |
| Referencias citadas | 32 |
The aetiology, symptoms, diagnosis and treatment of ME/CFS are controversial. Doctors and sufferers often have opposing perspectives, leading to problematic clinical interactions. We use discourse analysis to explore ME/CFS sufferers' descriptions of interactions with medical professionals taken from an asynchronous, online sufferers' support group. Participants described themselves as experiencing limited medical care and attention but restricted criticisms to 'legitimate', pragmatic or ancillary matters such as a clinicians' unwillingness to prescribe untested treatments. Participants also described themselves as active in seeking a resolution to their problems. They thus attended to possible negative attributions of being 'complaining' or unmotivated to seek recovery
Attribution · Chronic fatigue syndrome · Discourse analysis · Psychiatry · Psychotherapist · Fibromyalgia and Chronic Fatigue Syndrome Research · Medicine · Psychology · Clinical Psychology · Social Psychology
The interactional history of examples and parentheses
“Normally I Always Ask Briefly…”
Doing Recovery Online
From Social Isolation to Becoming an Advocate
The real me shining through M.E.”
Grieving Online
Compelled loneliness and necessitated social isolation
Austerity and identity formation
Attributions, distress and behavioural responses in the significant others of people with chronic fatigue syndrome
Expanding the Political Psychology Toolkit
Understanding medical students' views of chronic fatigue syndrome
A relational analysis of an invisible illness
The need for a standardized conceptual term to describe invalidation of patient symptoms
Social Psychology and Discourse
Discourse and Cognition
The Chronic Fatigue Syndrome
Chronic Fatigue Syndrome
Lectures on Conversation
Stories’ of chronic fatigue syndrome
Legends on the net
Computer-Mediated Communication
For she who knows who she is
Sharing Experiences of Contested Illness by Storytelling
Using the Online Medium for Discursive Research About People With Disabilities
"I'm a Bit Concerned"--Early Actions and Psychological Constructions in a Child Protection Helpline
Extreme Case Formulations
E-Scaped Medicine? Information, Reflexivity and Health
Extreme case formulations
Narrative Identities and the Management of Personal Accountability in Talk about ME
Moaning, whinging and laughing
Illness Intrusiveness in Myalgic Encephalomyelitis
Patient School as a Way of Creating Meaning in a Contested Illness
Doing things with illness. The micro politics of the CFS clinic
Chronic Fatigue Syndrome in Male Gulf War Veterans and Civilians
The Local Production of Knowledge
What is it like to have ME
Myalgic Encephalomyelitis and the medical encounter1
Doctor in the house
| Obras citantes distintas | 13 |
|---|---|
| Citas por año | 0,93 |
| Intervalo de citas | 2012 - 2024 (13) |
| Velocidad de citación | recent |
| Altamente citado | No |
| Tipos de cita | Neutras: 13 |