NATIONAL ALLIANCES for rare disease patient groups
A selection of National Alliances for rare disease patient groups in Europe and worldwide - www.eurordis.org
MORE INFORMATION on rare disease information services can be found in the RARE DISEASE SITES section of the Eurordis website.
ASK YOUR DOCTOR Eurordis cannot respond to questions concerning the medical aspects of a rare disease. Eurordis does not employ qualified medical personnel or information specialists to give medical advice, diagnose illness, or offer referrals.
We strongly recommend that you seek the advice of your health care provider with questions regarding medical care.
If you need help finding a patient group for your disease, email us at eurordiseurordis.org