volume 2, issue 8, PS433 2007
DOI: 10.1097/01.jto.0000283343.74967.96
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Abstract: The data from these focus groups should be viewed in light that the patients participating were all well enough to do so. Needs of people with more advanced disease (and their carers) may be different. Conclusions: This study contributes to increased understandings of the patient experience, and that of informal carers, to assist in the provision of information for decision making and in supporting patients in coping with NSCLC. These findings will also contribute to understandings of the experiences of NSCLC …

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