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Latest Blog Posts Tagged "Newsletters"

All in the Family

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.

The Kids Are All Right: Young Team Fox Members Get Creative 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.

A Note from Our CEO: How Genetic Research Illuminates the Path to Cures

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?

Going the Extra Miles with Team Fox

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.

Building the Base of Movement Disorder Specialists

November 16, 2017

MJFF and the Edmond J. Safra Foundation is funding two initiatives to bring more movement disorder specialists into the field.

A Note from Our CEO: Driving Research with Patient Power

November 14, 2017

The Sherer Report from the Fall/Winter 2017 edition of The Fox Focus, our biannual newsletter.

"Participating in Studies Gives One a Sense of Power"

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.

Getting Precise about Precision Medicine in Parkinson's

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.