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Abstracts

Quality of life in leaders and members of peer-led aphasia support groups – preliminary results of a systematic approach

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References

  • Attard, M., Lanyon, L., Togher, L., & Rose, M. (2015). Consumer perspectives on community aphasia groups: A narrative literature review in the context of psychological well-being. Aphasiology, 29, 983–1019.
  • Corsten, S., Schimpf, E., Konradi, J., Keilmann, A., & Hardering, F. (2015). The participants’ perspective: How biographic–Narrative intervention influences identity negotiation and quality of life in aphasia. International Journal of Language & Communication Disorders, 50, 788–800.
  • Engell, B., Hütter, B.-O., Willmes, K., & Huber, W. (2003). Quality of life in aphasia. Validation of a pictorial selfrating procedure. Aphasiology, 17, 383–396.
  • Hilari, K., & Northcott, S. (2016). “Struggling to stay connected”: Comparing the social relationships of healthy older people and people with stroke and aphasia. Aphasiology, 31, 674–687.
  • Rotherham, A., Howe, T., & Tillard, G. (2015). “We just thought that this was Christmas”: Perceived benefits of participating in aphasia, stroke, and other groups. Aphasiology, 29, 965–982.

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