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“I Wish Someone Had Once Asked Me How I’m Doing”: Disadvantages and Support Needs Faced by Parents of Long-Term Childhood Cancer Survivors
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“I Wish Someone Had Once Asked Me How I’m Doing”: Disadvantages and Support Needs Faced by Parents of Long-Term Childhood Cancer Survivors

This publication focuses on the parents’ perspective of childhood cancer survivors (CCS) and how cancer affects the whole family. Initially, the authors describe the parents' perspective by looking into the disadvantages and of their support needs during treatment, after treatment, and today. Secondly, the article focuses on the characteristics associated with disadvantages and support needs and lastly, with the use of existing support services.

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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.

Continue reading · Psychosocial Care“I Don’t Take for Granted That I Am Doing Well Today”: A Mixed Methods Study on Well-Being, Impact of Cancer, and Supportive Needs in Long-Term Childhood Cancer SurvivorsNowadays, most children can be cured from cancer and become survivors. This means that more survivors experience physical, social, and emotional difficulties after being cured. Still, few survivors get care that goes beyond the medical impact of cancer. The social and emotional wellbeing of survivors is often not addressed by healthcare professionals. Knowing about the unmet needs of survivors can give healthcare professionals important information on how to help survivors and also address their social or emotional problems and/or concerns. In this study, the authors have explored in-depth the experiences of survivors living in Switzerland on their wellbeing, impact of cancer and unmet needs in care. Results show that the majority of survivors has many unmet needs and indicates the current lack of specific psychosocial care. Hopefully, these findings will encourage healthcare professionals to develop services and provide care tailored to survivors’ unmet needs.

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