Childhood cancer affects the whole family and can have a lasting impact on parents of childhood cancer survivors (CCS). The authors aimed to describe parents’ perspectives of currently experienced disadvantages and of their support needs during treatment, after treatment, and today; to identify characteristics associated with disadvantages and support needs; and to describe the use of existing support services.
In this population-based study, the authors identified parents of CCS through the Swiss Childhood Cancer Registry (SCCR). Parents completed a questionnaire on perceived disadvantages (e.g., job-related, financial, etc.), support needs (e.g., job-related, financial, etc.), and socio-demographics. Cancer-related characteristics were available from the SCCR. The authors used multivariable multilevel logistic regression to identify characteristics associated with disadvantages and support needs.
As a result, an average of 24 years after diagnosis, one-fifth of parents reported disadvantages, and 7.1% reported support needs. Many parents desired more support during or after their child’s cancer treatment. Parents whose child experienced late effects or was dependent on parents reported greater current need for more support. Almost half of parents reported having used existing support services.
Many parents need more support during and after active treatment of their child’s cancer, and some experience support needs and disadvantages long into survivorship. Better promotion of existing services for parental and familial support and setting up new services, where needed, may help parents in the long term.
Ovaj članak pruža isključivo informativnu podršku i nije zamjena za profesionalni medicinski savjet, dijagnozu ili liječenje. Za medicinske odluke uvijek se posavjetujte sa svojim zdravstvenim djelatnikom.
Ovaj sadržaj nastao je tijekom projekta EU-CAYAS-NET, sufinanciranog u okviru programa EU4Health u razdoblju 2022-2025 (ugovor o dodjeli bespovratnih sredstava br. 101056918).
