PanCare is a multidisciplinary pan‐European network of professionals, survivors and their families that aims to reduce the frequency, severity and impact of late side‐effects of the treatment of children and adolescents with cancer. PanCare is working to achieve equity of access to care for childhood cancer survivors across Europe, to perform collaborative research and to act as a resource of research based information concerning all late side‐effects of cancer treatment. An important aim of PanCare is to work with the European Community to increase awareness and research about childhood cancer survivors. 

The mission of PanCare is to ensure equal access to optimal long-term care and to improve quality of life for every child and adolescent in Europe after their cancer treatment.

 

Upcoming meetings/events

  • PanCareLife PanCare Studies on Fertility and Ototoxicity to Improve Quality of Life after Cancer during Childhood, Adolescence and Young Adulthood (Peter Kaatsch) 2013-18  

  • PanCareSurFup - PanCare Childhood and Adolescent Cancer Survivor Care and Follow-up Studies (Lars Hjorth)

  • Educational Booklet - Paediatric haematooncological educational booklet (Edit Bárdi)

  • ENCCA - European Network for Cancer research in Children and Adolescents (Riccardo Haupt)

FAQ about PanCare

PanCare Committees

  • Advocacy, Awareness and Visibility Committee
  • Membership Committee
  • Newsletter Committe
  • Fundraising Committee
  • Website committee
  • Election Committee
  • Audit Committee
Should you wish to know more about PanCare Committees and Working Groups, please click here

 

 

 

 

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