The Italian Committee of Parkinson’s Associations was born from the need to join forces among the many national associations that are dedicated to support of Parkinson’s patients and their families.

It is no-profit and no-partisan, it aims to concretely improve the lives of people with Parkinson’s and their caregivers through:

• Coordination of as many existing Parkinson’s organization (association and ETS, social cooperative, University and Research Centre, Company, Workgroup, I.C.C.R.S., International Fundations (143 Italy + 26 Europe)
• Planning and implementation of communication and training tools to support sharing best practice, local activities, experiences, projects and resources
• Promotion of virtuous member projects making them available on national level, facilitating collaborations, partnerships, raising funds and optimizing resources
• Conduct a National pathology census
• Promote patient advocacy campain and petitions by social platform as Change.org and Facebook

The Committee is structured into a Directive Council made up of the President, Vice-President, Secretary and three managers, the operational headquarters of the Committee is in Verbania (VB

The Committee is organized into regional sections and, where not present, through partnership with other nolAmbassadors and Dopamine Hero who act as linkers and POPs (point of presence).

As provided in the STATUTE by article 5 “Endowment Fund”, the Committee is also authorized to receive sponsorships for projects and services.

Active member of:

Our projects:

National coordinator of
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