'Eating disorders are not about food, they're about life': Client perspectives on anorexia nervosa treatment.

Poor success rates and high levels of dropout are common features in the treatment of anorexia nervosa. Using semi-structured interviews, this study elicited the views of 12 women who were recovered, or in recovery, for anorexia nervosa and had received treatment. Results derived from a thematic analysis revealed the women's high degree of dissatisfaction with treatment and their perception that the treatment system is overly focused on, and driven by, food and weight.

"If I see somebody…I'll immediately scope them out": anorexia nervosa clients' perceptions of their therapists' body.

Although people with eating disorders are known to observe and assess body related stimuli, research has yet to explore these behaviors in the therapy room. Consequently, practitioners do not know if their bodies are having an impact on their clients or the therapy process. This lack of knowledge is problematic given the poor recovery rates and high levels of drop-out in eating disorders treatment.

Eating disorder counsellors with eating disorder histories: a story of being "normal".

Debate exists in the eating disorders field about the fitness to practise of counsellors with eating disorder histories (Johnston, Smethurst & Gowers, 2005). Yet despite widespread acknowledgement of the demanding nature of eating disorder counselling in general (Zerbe, 2008), almost no research exists about the actual experiences of recovered eating disorder counsellors in particular. Using semi-structured interviews this study aimed to address the research gap by investigating the experiences of 7 counsellors with eating disorder histories.

A qualitative exploration of carers' and 'patients' experiences of fibromyalgia: one illness, different perspectives.

Objectives: Previous research has largely focused on the lived experience either of those who have fibromyalgia syndrome (FMS) or their spousal carers. This study aimed to explore the lived experiences of both those with FMS and their spousal carers.

Methods: Participants were aged between 38 and 65 years and all came from the south-west of England.