Find support, or help research
People near you who know what living with Huntington's disease is like, and ways you can help find better treatments.
Support groups in Italy
- Associazione Italiana Corea di Huntington – Napoli ODVPatient association in Italy for people with Huntington's disease and their families; member of European Huntington Association.All of Italy
- Associazione Italiana Corea di Huntington – Roma ODVPatient association in Italy for people with Huntington's disease and their families; member of European Huntington Association.All of Italy
- Associazione Italiana Huntington Emilia Romagna – AIHER ODVPatient association in Italy for people with Huntington's disease and their families; member of European Huntington Association.All of Italy
- Huntington OnlusPatient association in Italy for people with Huntington's disease and their families; member of European Huntington Association.All of Italy
- Lega Italiana Ricerca Huntington e malattie correlate (LIRH)Italian foundation (league) for research on Huntington's disease and related disorders, also supporting families; member of the European Huntington Association.All of Italy
- NOI HuntingtonPatient association in Italy for people with Huntington's disease and their families; member of European Huntington Association.All of Italy
Contact details come from each group's own page and are checked every 3 months.
Help research
You do not need to join a trial to help. Below are the programmes we found in Italy and how to reach them. You contact them yourself: Frontlight does not collect or pass on your details.
Give blood or tissue for researchResearchers use stored samples to find what causes Huntington's disease.
Share your health dataA registry collects health data, without your name, so research teams can study many people at once.
Take part as a healthy volunteerStudies need people without Huntington's disease to compare with. Family and friends can help.