Latest Blog Posts Tagged "Newsletters"
June 06, 2018
Mike's father, Neil, lived with PD for a decade before passing away in 2012. His family came together to honor his memory through commitment to supporting research for a cure.
June 04, 2018
There's no age minimum (or limit) to join Team Fox. With 100 percent of proceeds going to speed a cure for Parkinson's, children and teens can make a real difference for the PD community.
May 31, 2018
At MJFF, we are investing tens of millions of dollars in genetic research. But how does a genetic finding become a direction to a new treatment?
November 20, 2017
In recent years, the PD community has led a groundswell of support and participation for Team Fox athletic events in their communities.
November 16, 2017
MJFF and the Edmond J. Safra Foundation is funding two initiatives to bring more movement disorder specialists into the field.
November 14, 2017
The Sherer Report from the Fall/Winter 2017 edition of The Fox Focus, our biannual newsletter.
June 02, 2017
Sue Lifschiz of Santa Rosa, California was diagnosed with PD in 2002. She joined PPMI to find a biomarker for earlier diagnosis and better disease tracking.
May 31, 2017
Prescribing therapies based on one's genes, environment and/or lifestyle - rather than a one-size-fits-all approach - can help people find treatments that work for them.
May 25, 2017
CEO Todd Sherer, PhD, talks research updates and the impact of MJFF during this critical juncture in Parkinson's research.
May 10, 2016
The Sherer Report from the Spring/Summer edition of The Fox Focus, our biannual newsletter.