EURORDIS

Patient Advocacy Sponsor

EURORDIS-Rare Diseases Europe is a unique, non-profit alliance of over 700 rare disease patient organisations from more than 60 countries that work together to improve the lives of the 30 million people living with a rare disease in Europe.
 
By connecting patients, families and patient groups, as well as by bringing together all stakeholders and mobilising the rare disease community, EURORDIS strengthens the patient voice and shapes research, policies and patient services.
EURORDIS' mission is to work across borders and diseases to improve the lives of people living with a rare disease
EURORDIS' vision to enable better lives and cures for people living with a rare disease
Follow @eurordis or see the EURORDIS Facebook page. For more information, visit www.eurordis.org


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