Multiple sclerosis and quality of life: A qualitative investigation

Journal of Health Services Research and Policy

Volumn 7, Issue 3, 2002, Pages 151-159

  Somerset, M ^a   Sharp, D ^a   Campbell, R ^a  

^a UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

QUALITY OF LIFE;

ADULT; AGED; ARTICLE; CHRONIC DISEASE; CLINICAL ARTICLE; DISABILITY; FEMALE; HAPPINESS; HUMAN; INDEPENDENCE; INTERVIEW; MALE; MULTIPLE SCLEROSIS; PRIORITY JOURNAL; QUALITATIVE ANALYSIS; QUALITY OF LIFE; SOCIAL BEHAVIOR;

ATTITUDE TO HEALTH; CAREGIVERS; CHRONIC DISEASE; COST OF ILLNESS; DISABLED PERSONS; GREAT BRITAIN; HUMANS; INTERVIEWS; MENTAL HEALTH; MULTIPLE SCLEROSIS; PATIENT PARTICIPATION; PERSONAL AUTONOMY; PROFESSIONAL-PATIENT RELATIONS; QUALITY OF LIFE; SOCIAL SUPPORT;

EID: 0036313827     PISSN: 13558196     EISSN: None     Source Type: Journal    
DOI: 10.1258/135581902760082454     Document Type: Article

References (32)

1. Neuropsychological aspects of multiple sclerosis
2. Multiple sclerosis: Assessment of disability and disability scales
3. The use of brain magnetic resonance imaging in multiple sclerosis
4. Interferon beta produces only small benefits in multiple sclerosis
5. Population based cost utility study of interferon beta-1b in secondary progressive multiple sclerosis
6. Treatment of multiple sclerosis with interferon beta: An appraisal of cost-effectiveness and quality of life
7. Burden of illness of multiple sclerosis. Part II: Quality of life
8. Exploring differences between subgroups of multiple sclerosis patients in health-related quality of life
9. Quality of life in multiple sclerosis: Measuring the disease effects more broadly
10. The psychosocial aspect of multiple sclerosis
11. Characterization of major depression symptoms in multiple sclerosis patients
12. Multiple sclerosis, depression, and suicide
13. Risk factors for suicide in multiple sclerosis
14. Helplessness, self-efficacy, cognitive distortions, and depression in multiple sclerosis and spinal cord injury
15. The relationship of appraisal and coping to chronic illness adjustment
16. The role of coping in adjustment to multiple sclerosis-related adaptive demands
17. Coming to terms with chronic illness: The negotiation of autonomy in rheumatoid arthritis
18. Care or empowerment? A disability rights perspective
19. Emancipating disability studies
20. The development of WHOQOL in the UK
21. Sampling for qualitative research
22. Emerging criteria for quality in qualitative and interpretative research
23. Reading and evaluating qualitative research studies
24. A hierarchy of reactions to disability
25. Health appraisal models in multiple sclerosis
26. Physician recommendations and patient autonomy: Finding a balance between physician power and patient choice
27. The relationship of social comparison to rheumatoid arthritis symptoms and affect