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PDF Research Advocates Guide $16 Million in Parkinson’s Research Funding

Recently, two Parkinson’s Disease Foundation (PDF) volunteers helped guide $16 million in government funding for Parkinson’s disease (PD) research.

This spring, Sam Erwin, M.S., M.A., of West Des Moines, IA, and Paul Zimmet, D.D.S., of Reston, VA – both PDF Research Advocates, people living with PD and US Army Veterans – served as consumer reviewers of research funded by the US Department of Defense (DoD).

They reviewed applications from scientists seeking funding through DoD’s Neurotoxin Exposure Treatment Parkinson’s Research program (NETPR). Working alongside scientists, Ms. Erwin and Dr. Zimmet shared their insights as to how the funding could be spent to effectively to advance science and improve the lives of people with Parkinson’s disease.

This is the first time individuals from PD community have participated as consumer reviewers.

“In light of PDF’s decade-long commitment to patient engagement, we are thrilled to see government organizations such as DoD taking steps to involve people living with Parkinson’s in research that impacts their disease. We applaud DoD, along with Ms. Erwin and Dr. Zimmet for working together to ensure patient priorities are part of research to end Parkinson’s,” said Veronica Todaro, M.P.H., Vice President, National Programs, PDF.

“As a person living with Parkinson’s who has served as a PDF Research Advocate for more than seven years, this experience reminded me that we as patients can make a real impact on research,” added Dr. Zimmet. “When it was time to make decisions about research proposals, my voice was not only heard, it was listened to and it was counted."

Ms. Erwin added, "It was exciting, as a PDF Research Advocate, represent my state, my military branch and most importantly, women with Parkinson’s disease. I was able to bring these various perspectives to the table when sharing my insights on which research is most important to those of us living with Parkinson's."

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Parkinson’s Foundation Announces New Genetic Initiative Connecting Parkinson’s Genetic Data with Clinical Care
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MIAMI & NEW YORK—March 6, 2018—The Parkinson’s Foundation today announced a new initiative offering genetic testing and counseling to Parkinson’s patients within its Center of Excellence network.

Delegates From The Parkinson’s Community Converge On Capitol Hill To Advocate For Critical Research Funding
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—2018 Parkinson’s Policy Forum Co-Sponsored by the Parkinson’s Foundation and the Michael J. Fox Foundation for Parkinson’s Research—

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