1. Scope of the project
  2. Why is this project important for the rare disease community?
  3. Objectives of the project
  4. Role of EURORDIS
  5. Outcomes of the project

Scope of the project

INNOVCare (Innovative Patient-Centred Approach for Social Care Provision to Complex Conditions) addresses the social challenges faced by rare disease patients and the gaps in the coordination between medical, social and support services in European Union Member States.

This EU-funded project will give voice to the social needs of people living with a rare disease. It will support the EU and Member States in implementing necessary structural reforms in social care systems by developing and testing a holistic, personalised care pathway.

Why is this project important for the rare disease community?

Rare diseases often do not have a satisfactory treatment or any treatment at all. As a result, the need for integrated care provision is crucial to alleviate the impact that a rare disease has on the daily life of the patient and their family. 

The innovative care pathway developed under INNOVCare involves linking health services to employment and the social and support services that a rare disease patient uses on a daily basis (school, transport, leisure services etc.), ensuring the transfer of information and expertise between service providers.

The care pathway also centralises the coordination of care through a resource centre for rare diseases and regional case managers, in an effort to relieve the burden of care management for people living with a rare disease and their families.

Objectives of the project

  • Assessment of unmet social needs of people living with a rare disease and their families in Europe and analysis of existing care models in a selection of EU Member States;
  • Proposal of an innovative care pathway bringing together national resource centres for rare diseases and regional case managers, in partnership with public bodies:
    • Implementation of a pilot of this pathway in Romania;
    • Evaluation of the socio-economic impact and a cost-benefit analysis of the care model;
    • Exchange of good practices between resource centres gathered in an European network of services;
  • Analysis of opportunities to upscale the model to other Member States and beyond rare diseases;
  • Strengthening partnerships between public, private and civil society organisations.


  • Communication, including the coordination of the internal and external communication of the project as well as the organisation of the ad-hoc advisory group;

  • State-of-the-art analysis of the social needs of people with rare diseases and of social care in Member States, through a European-wide survey (see results report and infographic) and the study of care pathways in a selection of Member States;

  • Facilitation of the creation and governance of a  European network of resource centres for rare diseases and the  organisation of meetings for exchange of good practices;
  • Representation of people living with a rare disease and their families in coordination with EURORDIS’ members and with EURORDIS Social Policy Advisory Group;
  • Ensuring the link between INNOVCare, the rare disease community, key EU rare disease projects and relevant stakeholders (through the new RD-Action and the Commission Expert Group on Rare Diseases).

Outcomes of the project


This project is co-funded by the European Union
This project is co-funded by
the European Union


The information contained in this publication does not necessarily reflect the official position of the European Commission.

Page created: 17/11/2015
Page last updated: 05/11/2019
La voix des patients atteints de maladies rares en EuropeEURORDIS Donnant la voix, à l'international, aux personnes vivant avec une maladie rareRare Disease International Pour rapprocher patients, familles et experts sur un forum modéré multilingue, où partager leurs expériences. RareConnect Le programme Rare Barometer est une initiative d’EURORDIS qui vise à réaliser des sondages pour transformer les expériences des patients de maladie rare en faits et chiffres à communiquer aux décideurs politiques.Rare Barometer Campagne internationale de sensibilisation organisée chaque année le dernier jour de février, la Journée Internationale des Maladies Rares est une initiative d'EURORDISRare Disease Day Participez au plus grand événement réunissant tous les acteurs des maladies rares en Europe lors de Conférence européenne bisannuelle sur les maladies rares et les médicaments orphelins (European Conference on Rare Diseases and Orphan Products, ou ECRD). L'ECRD est une initiative d'EURORDISEuropean Conference on Rare Diseases