Choose your country from the menu http://www.euro-hd.net/html/network/locations and select the respective coordination centre. There you find contact details (names, address, e-mail, and phone numbers). Alternatively, you may use the contact form provided on http://www.euro-hd.net/html/network/communication/contact.

You can make an appointment either by referral from your general practitioner or by directly contacting a neurologist via your language coordinator (www.euro-hd.net/html/network/project/langcoord).

Independent advice about HD can be obtained from the lay organisation of your country. Choose your country from the menu http://www.euro-hd.net/html/network/locations and select the respective HD Association. A list of national HD lay organisations is provided on www.euro-hd.net/html/disease/links/hdas.

The EHDN hosts the largest European HD study, which is called REGISTRY (www.euro-hd.net/html/registry). REGISTRY is accessible at many study sites across the continent. To find out if there is a site near you, please visit the location (www.euro-hd.net/html/network/locations) section of this website and approach your local public contact. You can also contact your language coordinator (www.euro-hd.net/html/network/project/langcoord) who will be able to update you on research activities within your region. It is also possible for you to contact your local lay organisation (www.euro-hd.net/html/disease/links/hdas) to find out more about participating in research. Click here for more information and links to HD research (http://www.euro-hd.net/html/disease/links).

There are several lay organisations that provide support for individuals and families affected by HD. These organisations can be reached via your general practitioner or HD specialist. There is a list of HD support associations on the EHDN website. To access them, click on the link www.euro-hd.net/html/disease/links/hdas