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INTRODUCTIONWorldwide, about 18 million people are newly diagnosed with cancer annually (Ferlay et al., 2019). The confrontation with this life‐threatening disease is associated with a high level of psychosocial distress (Carlson et al., 2019). After the diagnosis treatment, short‐term decisions must be made. Oncological treatment is accompanied by various short‐ or long‐term side effects (Schirrmacher, 2019). Fear of recurrence or progression and depression are the most common issues of cancer survivors (Götze et al., 2019). Various types of psychosocial care are available to help patients cope with the sequelae of the illness. As an example, sharing experiences in cancer self‐help groups (CSHG) can promote realistic expectations about the medical treatment, and consequences of the disease thus may be interpreted in terms of problem‐oriented coping as well as social downward comparison (Taylor et al., 1990). Expecting that another person is worse off may help oneself to feel better. Cancer patients utilise various forms of peer support like face‐to‐face or online groups or one‐to‐one consultation. In this context, peer support can be understood as social relationships created and initiated by affected persons to offer mutual support (Dennis, 2003). In Dunn's approach, peer led CSHGs are defined as ‘peer‐supervised’ and in ‘face‐to‐face settings’ without any professional supervision (Dunn
European Journal of Cancer Care – Wiley
Published: Nov 1, 2022
Keywords: cancer; peer support; psychosocial support; qualitative methods; review; self‐help group
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