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The EPDA is the only European Parkinson's disease umbrella organisation. Our members are national Parkinson's disease organisations from 36 countries across Europe and we advocate for the rights and needs of more than 1.2 million people with Parkinson's and their families.

The EPDA vision

Our vision is to enable all people with Parkinson’s in Europe to live a full life while supporting the search for a cure.

The EPDA mission

In order to make our vision a reality, we aim to become the leading voice for Parkinson’s in Europe by providing innovative leadership, information and resources to:

national Parkinson’s organisations European policymakers healthcare professionals people with Parkinson's and their families treatment industry the media

We hope to raise the profile of Parkinson’s and enable people living with the disease to be treated effectively and equally throughout Europe.

What does the EPDA aim to do?

By working with our members – who represent the needs of individual people with Parkinson’s and their families at a national level – the EPDA aims to:

positively influence Parkinson’s stakeholders to challenge existing mindsets, shift attitudes and remove the hurdles that prevent PwPs from receiving early and appropriate treatment as well as individualised care increase public and political awareness of Parkinson’s as a priority health challenge support the development of national Parkinson’s organisations throughout Europe help reduce stigma and remove discrimination against people with Parkinson’s

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