‘You don't get told anything, they don't do anything and nothing changes’. Medicine as a resource and constraint in progressive ataxia
Article first published online: 24 OCT 2012
© 2012 Blackwell Publishing Ltd
How to Cite
Daker-White, G., Kingston, H., Payne, K., Greenfield, J., Ealing, J. and Sanders, C. (2012), ‘You don't get told anything, they don't do anything and nothing changes’. Medicine as a resource and constraint in progressive ataxia. Health Expectations. doi: 10.1111/hex.12016
- Article first published online: 24 OCT 2012
- Manuscript Accepted: 18 SEP 2012
- chronic illness;
- clinical uncertainty;
- existential uncertainty;
- limits of medicine;
- rare diseases
Progressive ataxias are neurological disorders affecting balance, co-ordination of movement and speech.
A qualitative study was undertaken to discover patients' experiences of ataxia and its symptoms.
Thirty-eight people with ataxia recruited from patient support groups and two hospital outpatients departments.
Cross-sectional qualitative study with thematic analysis.
These accounts highlight the limits of medicine in the context of a rare, incurable and disabling disorder, and the embodied uncertainties brought by slowly progressive diseases that lie at the boundaries of mainstream medical knowledge. The existential crises faced by people with ataxia are seemingly magnified by sometimes idiopathic aetiologies and the limited number of inherited conditions identifiable by the available genetic tests. Interviewees were drawn into a medical system that was focused mainly on the diagnosis process, with widely varying results. However, when asked, most had rather valued the provision of disability aids and physical therapies. Only one informant reported overcoming the myriad uncertainties of progressive ataxia, and their account supported the notion of ‘biographical repair’ in chronic illness.
Clinical uncertainties in ataxia constrained people's attempts to deal with their condition. The construction of the proactive, informed, medical consumer who is assumed to be a partner in care is problematic in the context of a rare and difficult-to-diagnose disease for which there is usually no cure. Service providers should be mindful of the need to manage patient expectations in relation to diagnosis and cure. More focus might usefully be placed on the provision of physical therapies and disability aids.