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Background Previous studies suggest that adolescents with JIA cope relatively well with the consequences of their painful and potentially incapacitating illness, and that, with regard to their psychosocial functioning, there seem to be few differences between them and healthy teenagers. The discrepancy between these findings and clinical experience gave us reason to search for a more subtle care and research method directly related to the adolescent patients' own experience. In this study, it is assumed that a person consists of different self-positions, ordered into a flexible and varied hierarchy that can alter over time, and in accordance to the demands of diverse contexts. Chronic illness could possibly lead to a more one-sided organization of a person's experience.

Psychological impairment in adolescents with JIA: should we continue the search for evidence?