Ann Johnson and Team Annie
Please click here to enjoy these pictures from a beautiful walk day at the 2011 Nashville Walk for PKD!
Learn More About PKD.
Don’t miss out on our series of quarterly webinars designed to provide education and information about various medical and lifestyle issues related to polycystic kidney disease.
Click here to visit our NEW learning center and to view our FREE educational webinars!
Make a difference in the lives of 12.5 million people.
Did you know that the lion’s share of money for PKD research comes from the federal government funding? More than 600,000 people suffer from PKD, yet it receives less in federal research funding than other far less prevalent genetic diseases. We need a volunteer to head up our Advocacy and Awareness Leadership position who will take an interest in how we as grass-roots citizens can help raise the standard of money allotted to PKD by the U.S. government. Could it be you? Our staff PKD Advocated in Washington D.C. is looking for volunteers to help promote this need to our government officials. Please think about devoting time to this very important issue.