Exploring expressions of abandonment and rejection that emerged from group therapy with fibromyalgia patients

Fibromyalgia is a complex syndrome of diffuse pain associated with non-restorative sleep, fatigue, numerous tender points, depression and other conditions that often does not respond well to treatment posing a dilemma to health professionals. The aim of this study was to explore expressions of abandonment and rejection that emerged from group therapy with eleven fibromyalgia patients at the former Princess Alice Orthopaedic Hospital, Cape Town. It focused on abandonment/rejection by caregivers during childhood, death as a form of abandonment, abandonment/rejection in adulthood by family, spouse and family-in-law, by friends, colleagues and employers, by government and society, the hospital and doctors, and by fellow group members and the facilitator. The study is exploratory, interpretative and explanatory in nature with a purposive non-probability sample. The qualitative research method was used to gain insight into the subjective experiences of the lives and illness of the participants. The method of data collection was mainly the tape recorded and transcribed words of the participants over thirty-three group therapy sessions in eleven months and observations by the researcher as full participant observer. The data was sorted and analysed into emerging themes, patterns and categories. All participants had had repetitive experiences of abandonment/rejection, which they had denied, suppressed and avoided, as it was too painful. Due to a lack of inner and external resources, or any intervention, feelings of abandonment, fear and anger were internalized as an unresolved reservoir of emotional pain. This seemed to have escalated into an eventual expression of physical pain (somatisation). From the findings of this study, there appears to be a relationship between adverse psychosocial factors and stress, particularly experiences of abandonment/rejection and fibromyalgia. However, due to the qualitative nature and small sample, the findings cannot be extrapolated and generalized to the broader population of fibromyalgia patients, and quantitative studies are needed for verification.

Grantor dc:publisher.institution

Department of Social Development

Year dc:date.issued

2003

Author dc:creator

• Van der Walt, Ria

Advisor dc:contributor.advisor

• Graser, Roland

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/11427/6941

OAI identifier oai:identifier

oai:open.uct.ac.za:11427/6941