The Parkinson’s Disease Foundation (PDF) is a leading national presence in Parkinson’s disease research, education and public advocacy. We are working for the nearly one million people in the US who live with Parkinson’s disease (PD) by funding promising scientific research to find the causes of and a cure for Parkinson's while supporting people with Parkinson’s, their families and caregivers through educational programs and support services. Since its founding in 1957, PDF has funded over $80 million worth of scientific research in Parkinson’s disease, supporting the work of leading scientists throughout the world.
At the heart of PDF's work is the participation of people with Parkinson's. Whether it is through our People with Parkinson's Advisory Council, which advises us on all projects, or the Clinical Research Learning Institute, which trains people with PD to play a part in clinical research - the perspective of people living with Parkinson's ensures that our work is on target and meets the needs of the community.
Research
Central to the mission of the Parkinson’s Disease Foundation (PDF) is funding research of the highest caliber. Through our diverse research programs, there is a single underlying objective: to identify and support the most promising Parkinson’s disease science.
Education
The mission of the Parkinson's Disease Foundation is not only to pursue the cure for Parkinson’s but also to provide assistance to the people who live with the disease. A top priority for PDF remains the dissemination of accurate, accessible information about Parkinson’s to people with the disease and their families. Through our innovative educational programs, PDF remains a trusted source of Parkinson’s information. Through outlets such as our Parkinson’s Information Service (PINS), a “one-stop shop” for the Parkinson’s disease community, our team of information specialists can answer questions about Parkinson’s via our toll-free helpline, (800) 457-6676, and our “Ask the Expert” web service.
Advocacy
For more than a decade, the Parkinson’s Disease Foundation has assumed the role of public advocate on behalf of, and in collaboration with, people with Parkinson’s, their families and caregivers. One example is thorugh training people with Parkinson’s to educate and empower the broader community about the importance of Parkinson’s clinical research through our Clinical Research Learning Institute, an annualmulti-day educational seminar.