For anyone living in Europe who might not know this, on the Euro HD Project
website there is a section for Patients and relatives to contact the project
and ask questions:
http://www.euro-hd.net/html/network/communication/contact

This link is to a form that allows you to anonymously contact EHDN for
advice and for help in getting in touch with experts on HD.

Who can get in touch with the European HD Network?

If you are..
a patient suffering from HD?
at risk for HD?
a relative of an HD patient?

Do you want to..
contribute to a better understanding of HD?
make yourself available for studies in HD?
participate in drug trials in HD?

COOOOL IDEA!