The EpiCARE Patient Group (ePAG, European Patient Advocacy Group) gathers Patient representatives and Patient Organisations in rare and complex epilepsies who will ensure that patient voice is heard and implemented throughout the ERN development process. Patient organisations can become ePAG member organisations and patients can become ePAG representatives. If you are interested in becoming a member organization or an EPAG representative then please contact us via email. For further information, please consult the EURORDIS website. The Patient Group enables Patient representatives to work together on common issues and deliverables, as well as being involved in all EpiCARE activities. The Patient Group has two Chairs, ePAG representatives and ePAG members.