Why We Run…

We have decided to join the Run for PKD to help raise funds for polycystic kidney disease. Our grandfather has battled with the disease for many years and our mom has also been diagnosed. Since it is a genetic disease, it will continue to impact our family. We hope that with every step we run on October 10 in the Hartford Half Marathon, we will be one step closer to a cure. Thank you for your support!

Polycystic kidney disease is one of the most common life-threatening genetic diseases, affecting more people than Down syndrome, cystic fibrosis, muscular dystrophy and sickle cell anemia - combined. Currently there is no treatment and no cure… But there is hope.

The PKD Foundation is here to ensure that someday, no one suffers the full effects of PKD. The PKD Foundation aggressively seeks to convert:

• Ignorance into knowledge through high quality patient education materials

• Despair into hope through communications, support groups and research advances

• Isolation into community by involvement in more than 70 PKD Foundation chapters and by lobbying congress

• Ideas into reality through the research the Foundation funds and through clinical drug trials

• Basic science into therapies through ‘translational’ grants and the Foundation’s work with FDA

• Small dollars into large dollars by leveraging grants into expanded PKD National Institute of Health (NIH) research through ‘passionate advocacy’


And it is your financial support that makes this all possible. Please help me make a difference by making a donation today!