Janice M. Morse

Qualitative Significance
Qual Health Res 2004 14: 151-152. [PDF]  

Jenny Cheung and Peta Hocking

The Experience of Spousal Carers of People with Multiple Sclerosis
Qual Health Res 2004 14: 153-166. [Abstract] [PDF] [References]  

Karen Lowton

Only when I Cough? Adults’ Disclosure of Cystic Fibrosis
Qual Health Res 2004 14: 167-186. [Abstract] [PDF] [References]  

Linda Rozmovits and Sue Ziebland

Expressions of Loss of Adulthood in the Narratives of People with Colorectal Cancer
Qual Health Res 2004 14: 187-203. [Abstract] [PDF] [References]  

Mary Ann Meeker

Family Surrogate Decision Making at the End of Life: Seeing them Through with Care and Respect
Qual Health Res 2004 14: 204-225. [Abstract] [PDF] [References]  

Pia Åsbring and Anna-Liisa Närvänen

Patient Power and Control: A Study of Women with Uncertain Illness Trajectories
Qual Health Res 2004 14: 226-240. [Abstract] [PDF] [References]  

Heather Schacht Reisinger

Counting Apples as Oranges: Epidemiology and Ethnography in Adolescent Substance Abuse Treatment
Qual Health Res 2004 14: 241-258. [Abstract] [PDF] [References]  

P. Lynne Johnstone

Mixed Methods, Mixed Methodology Health Services Research in Practice
Qual Health Res 2004 14: 259-271. [Abstract] [PDF] [References]  

Marilys Guillemin

Understanding Illness: Using Drawings as a Research Method
Qual Health Res 2004 14: 272-289. [Abstract] [PDF] [References]  

Irena Madjar

Book Review
Qual Health Res 2004 14: 290-291. [PDF]  

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