Patient Power and Control
A Study of Women with Uncertain Illness Trajectories
Datos Bibliográficos
| ID | 5454746 |
|---|---|
| Autores | Pia Åsbring (Karolinska Institutet), Anna-Liisa Närvänen (Linköping University) |
| Año | 2004 |
| Volumen | 14 |
| Número | 2 |
| Páginas | 226-240 |
| Fecha de publicación | 2004-02-01 |
| Peer Reviewed | Sí |
| Open Access | Sí |
| Tipo | ARTICLE |
| Revista | Qualitative Health Research (JOURNAL) |
| Identificadores de la revista | ISSN: 1049-7323 • E-ISSN: 1552-7557 |
| Editorial | SAGE Publications Inc (PUBLISHER) |
| DOI | 10.1177/1049732303260682 |
| PMID | 14768459 |
| OpenAlex | W2140045187 |
| Idioma | EN |
| Citas recibidas | 24 |
| Referencias citadas | 46 |
The authors interviewed 12 women diagnosed with chronic fatigue syndrome and 13 with fibromyalgia with the aim of determining the strategies they perceive themselves as using to gain control over their situation during the health care process. The results highlight various strategies that the women report applying to find a way of managing the illness and to influence caregivers. They describe, for example, how they try to gain control over their situation by acquiring knowledge about the illness. The women also describe various power strategies they use in their interaction with the caregivers to take command of their situation, namely exiting, noncompliance, confrontation, persuasion/insistence, making demands, and demonstrative distancing
Disease · Distancing · Fibromyalgia · Health care · Illness behavior · Persuasion · Psychiatry · Sociology of health and illness · Clinical Psychology · Computer Science · Fibromyalgia and Chronic Fatigue Syndrome Research · Health, psychology, and well-being · Medicine · Mental Health and Psychiatry · Psychology · Social Psychology
Integrating social representations of nature in the study of tick-borne diseases risk
Meanings of Feeling Well for Women With Fibromyalgia
Power as equal ability, knowledge and resistance
Dismissing chronic illness
Factors impacting the illness trajectory of post-infectious fatigue syndrome
Making Sense of Gynecologic Cancer
The biopolitics of CFS/ME
Women in health
Medication and the patient–doctor relationship
Personal Agency and Community Resilience
An exploratory study of the experience of fibromyalgia diagnosis in South Africa
Online Health Information Seeking in the Context of the Medical Consultation in Switzerland
Nothing and Everything
Circuit Breaking
Staying Healthy From Fibromyalgia Is Ongoing Hard Work
Living With and Treating Rare Diseases
Occupational Overuse Syndrome
Doctor-Patient Relationship Between Individuals With Fibromyalgia and Rheumatologists in Public and Private Health Care in Mexico
I Had to Make Them Feel at Ease
A Psychological Perspective of Eye Floaters
Rhetorical work and medical authority
Illness experience in fibromyalgia syndrome
Words about body and soul
From embodiment to evidence
Chronic illness – a disruption in life
The Chronic Fatigue Syndrome
The american college of rheumatology 1990 criteria for the classification of fibromyalgia
Stress
The Discovery of Grounded Theory
Chronic Illness and the Quality of Life
Health, Illness and the Social Body. A Critical Sociology (Book)
Modernity and Self-Identity
Claiming Power in Doctor–Patient Talk
Patients' Views of Medical Practice
Original Article
Strategies for empowering women's voices in the medical culture
The sociology of chronic illness
Consumerism in Medicine
Unending Work and Care
Modifying the treatment
Negotiating Reality
Chronic Fatigue, Chronic Fatigue Syndrome, and Fibromyalgia
Public Challenge of Physician Authority
Basics of Qualitative Research
Going to See the Doctor
Seeking Validation
Women's Experiences of Stigma in Relation to Chronic Fatigue Syndrome and Fibromyalgia
Patients with medically unexplained symptoms
The meaning of medications
Ideal versus reality
Empowering patients
Patients' perceptions of medical care in chronic fatigue syndrome
Suffering, hope and diagnosis
Medicalization and Social Control
The Definition of the Situation
Exploring the Meaning of 'Dissatisfaction' with Health Care
Myalgic Encephalomyelitis and the medical encounter1
| Obras citantes distintas | 24 |
|---|---|
| Citas por año | 1,33 |
| Intervalo de citas | 2008 - 2026 (19) |
| Velocidad de citación | current |
| Altamente citado | No |
| Tipos de cita | Neutras: 23 |