Ideal versus reality
Physicians perspectives on patients with chronic fatigue syndrome (CFS) and fibromyalgia
Dados Bibliográficos
| ID | 4593702 |
|---|---|
| Autores | Pia Åsbring (Karolinska Institutet), Anna-Liisa Närvänen (Linköping University) |
| Ano | 2003 |
| Volume | 57 |
| Fascículo | 4 |
| Páginas | 711-720 |
| Data de publicação | 2003-08-01 |
| Peer Reviewed | Sim |
| Open Access | Sim |
| Tipo | ARTICLE |
| Periódico | Social Science & Medicine (JOURNAL) |
| Identificadores do periódico | ISSN: 0277-9536 • E-ISSN: 1873-5347 |
| Editora | Elsevier BV (PUBLISHER) |
| DOI | 10.1016/s0277-9536(02)00420-3 |
| PMID | 12821018 |
| OpenAlex | W2041195282 |
| Idioma | EN |
| Citações recebidas | 46 |
| Referências citadas | 33 |
Categorization · Chronic fatigue · Chronic fatigue syndrome · Disease · Etiology · Fibromyalgia · MEDLINE · Physical therapy · Psychiatry · Sick role · Fibromyalgia and Chronic Fatigue Syndrome Research · Health, psychology, and well-being · Medicine · Psychology · Psychosomatic Disorders and Their Treatments · Internal Medicine
Mapping the Social Organisation of Neglect in the Case of Fibromyalgia
Contesting Lyme Disease
Patient-made knowledge networks
Examining the psychology of practitioners, institutions and structures
Epistemic injustice suffered by patients with rare diseases, poorly understood diseases, and underdiagnosed diseases, and the epistemic advantage granted by these diseases
Medication and the patient–doctor relationship
Do Metaphors Matter? Fibromyalgia and Women's Embodiment
Questioning Biomedicine's Privileging of Disease and Measurability
The Social Course of Fibromyalgia
Social support needs for equity in health and social care
Factors impacting the illness trajectory of post-infectious fatigue syndrome
The association between Post-Covid syndrome and self-stigma among the adult Israeli population during the Covid-19 pandemic
Fatigue as a Major Predictor of Quality of life in Women with Autoimmune Liver Disease
The circuit of symbolic violence in chronic fatigue syndrome (CFS)/myalgic encephalomyelitis (ME) (I)
A Qualitative Natural History Study of ME/CFS in the Community
Diagnosis
Causes of Death Among Patients With Chronic Fatigue Syndrome
Bodies in lockdown
Dismissing chronic illness
Facing ignorance
Views from the Margins
Gatekeeping disability income support
Betwixt and between’; liminality in recovery stories from people with myalgic encephalomyelitis ( ME ) or chronic fatigue syndrome ( CFS)
Approaching recovery from myalgic encephalomyelitis and chronic fatigue syndrome
Patient Power and Control
Understanding medical students' views of chronic fatigue syndrome
Self within a climate of contention
I am not the kind of woman who complains of everything
Out of Chaos-Meaning Arises
Living With a Contested, Stigmatized Illness
Medical Residents' Experiences With Medically Unexplained Illness and Medically Unexplained Symptoms
Doctor-Patient Relationship Between Individuals With Fibromyalgia and Rheumatologists in Public and Private Health Care in Mexico
Rhetorical work and medical authority
Complex syndromes, ambivalent diagnosis, and existential uncertainty
Exploring the altered daily geographies and lifeworlds of women living with fibromyalgia syndrome
The tired hero and her (il)legitimation
Creating meaning in fibromyalgia syndrome
Quest, chaos and restitution
Difficult encounters with a hemophilic patient
The pain of being misunderstood
What is it like to have ME
Electronic Support Groups, Patient-Consumers, and Medicalization
I Never Wanted to Be a Quack
Debating the legitimacy of a contested environmental illness
Compelled loneliness and necessitated social isolation
Illnesses you have to fight to get
Chronic illness – a disruption in life
The Chronic Fatigue Syndrome
The american college of rheumatology 1990 criteria for the classification of fibromyalgia
Chronic Fatigue Syndrome
Deviance and medicalization
The Presentation of Self in Everyday Life
The Discovery of Grounded Theory
Outsiders
Medical and sociological typologies
Disease and illness Distinctions between professional and popular ideas of sickness
Getting Rid of Patients
Basics of Qualitative Research
Basics of Qualitative Research
Women's Experiences of Stigma in Relation to Chronic Fatigue Syndrome and Fibromyalgia
Doing things with illness. The micro politics of the CFS clinic
Patient characteristics negatively stereotyped by doctors
Profession of Medicine
Doctor-patient negotiation of cultural assumptions
Clinical uncertainty
Uncertainty and Professional Work
| Obras citantes distintas | 46 |
|---|---|
| Citações por ano | 2,09 |
| Intervalo de citações | 2004 - 2026 (23) |
| Velocidade de citação | current |
| Altamente citado | Não |
| Tipos de citação | Neutras: 45 |