With increasing survival rates in pediatric oncology, the medical and
psychosocial costs of cure are becoming apparent for the child and his
family. The focus of our concern is now how to prevent and to reduce
these adverse late effects of cancer and its treatment. To reduce the
late psychosocial consequences for the child and its family a booklet
was written for parents. We decided to address parents because of the
young age of many children when treatment is completed, the essential
role of parents in alleviating late effects for the child and his sibl
ings, and the possibility to discuss the whole range of psychosocial l
ate effects: those for the patient, the siblings, and for the parents
themselves. The booklet acknowledges the specific emotional problems i
n patients, parents, and siblings that results from surviving childhoo
d cancer and provides information and support on how to deal with them
. The booklet can enhance open communication with the health care team
about late consequences. In this way the booklet supports the further
integration of medical and psychosocial aftercare.