"

The project aims to establish a mechanism for timely, effective, and functional monitoring of the late effects of cancer in children and their families. The project's fundamental goal is identifying the most common complications after cancer treatment and finding ways to reduce or prevent them. Key project activities include: Survey and collection of patient data to identify the most common complications after treatment; Round table ""The role of CSOs and health institutions in the follow-up of persons treated for childhood cancer""; Organization of a two-day workshop for stakeholders from the health sector; Promotion and education about the late consequences of childhood cancer treatment among patients, medical staff and the general public; Creation of a publication on the most common late effects."