Read Katie Hood's Blog on The Huffington Post: The Patient Empowerment Revolution
In the wake of Google co-founder Sergey Brin's disclosure that he carries a genetic mutation increasing his risk for Parkinson's disease, Katie Hood blogs on the potential of genetic research to empower all of us to take ownership of our medical futures.
Katie Hood Appointed to NINDS Council
Katie Hood, chief executive officer of The Michael J. Fox Foundation for Parkinson’s Research, is one of four new members appointed to the NINDS Council, the major advisory panel to The National Institute of Neurological Disorders and Stroke (NINDS). She will serve through July 2012.
Save the Date: Research Roundtable in Chicago on October 21
The Michael J. Fox Foundation invites you to attend a Research Roundtable presentation titled "The MJFF Funding Philosophy and Research Portfolio Highlights."
