Six Action Steps to Address Global Disparities in Parkinson Disease
Six Action Steps to Address Global Disparities in Parkinson Disease
A World Health Organization Priority
3 Minute Test to Diagnose Parkinson’s Disease
Joy Milne is known the world over as the woman who can smell Parkinson’s. PD Avengers President Larry Gifford talked with her and Professor Perdita Barron, the Director of the Michael Barber Centre for Collaborative Mass Spectrometry at The University of Manchester, who’ve been working side by side hand to nose for years identifying what exactly it is that Joy smells and if it can be used as a way to diagnose Parkinson’s.
Planning for Prevention of Parkinson’s
Join us at the Liberty Hotel in Boston, MA or online from Sunday, October 2nd to Monday, October 3rd to explore and help shape designs for the first therapeutic trials to pursue Parkinson's disease prevention. View the agenda updated with new advocacy, regulatory, and industry perspectives.
PD AVENGERS MEMBER SPOTLIGHT
When were you/loved one first diagnosed?
My name is Rob Warner and I was diagnosed with Early Onset Parkinson’s Disease in 2007 when I was 33 years old.
Why did you want to become a PD Avenger?
I can’t remember how I came across the book “Ending Parkinson’s Disease” but after reading it I wanted to March on Washington! Non-violently of course but I didn’t know how to do it. But when listening to Larry Gifford’s podcast, “When LIfe Gives You Parkinson’s” and hearing he had started the PD Avengers I knew I wanted to be a part of such an awesome organization whose main focus is to end Parkinson’s.
The Bill To End Parkinson’s
“The most comprehensive, boldest, widespread piece of legislation specific to Parkinson’s disease ever introduced in the history of the U.S. congress.” — Ted Thompson, SVP Public Policy, The Michael J. Fox Foundation
PD Avengers Assemble - July 2022
Updates on Paraquat Lawsuits, PMD Alliance’s “All In” Conference, the inaugural Improv for Parkinson’s Summit, Every Victory Counts guide now available in Canada thanks to a collaboration between Davis Phinney Foundation and Parkinson’s Canada and more.

