What does it do?

  • It was created to care for all children affected by liver disease or who are liver transplant patients.
  • Its main activity is to provide psychological support, accommodation for affected families, awareness campaigns and an information and training centre for relatives who have to live with this disease.
  • The association wants to stand by their side in this process, represent and defend their rights and needs and promote actions and resources that help to improve their quality of life and that of their families.

What countries does it work in?

  • It is a national association and operates in Spain.

Other information of interest

  • One of its main functions is psychological support. It provides counselling and emotional support as well as therapies to treat anxiety and depression for both patients and their families.
  • They organise initiatives to promote communication and coordination between different hospitals that treat childhood liver disease.
  • They also collaborate so that the Paediatric Hepatology services have enough human, technical and material resources needed to carry out their work properly.

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