Outcomes

 

Short-term:
• An IT infrastructure for the European Register for Multiple Sclerosis (EUReMS);
• An IT platform for collaboration and dissemination of knowledge on multiple sclerosis (MS);
• A critical mass of national and regional MS centers for collaborative and sustainable European research in this field;
• Contributions to EU policies.

Long-term:
• Higher awareness of MS among both clinicians and general public in the European Union;
• Improved knowledge and management of MS;
• Sense of community for affected people and their families.