EURORDIS – Rare Diseases Europe

Global Genes Global Advocacy Alliance member focused on rare disease support, education, advocacy, or research. EURORDIS – Rare Diseases Europe is a non-profit alliance of over 1000 rare disease patient organisations from 74 countries that works across borders and diseases to improve the lives of all people living with rare diseases. Directory information only; not medical advice, legal advice, or endorsement. Services and eligibility should be confirmed with the organization.