PKD Foundation

Overview

The PKD Foundation is the only organization, worldwide, dedicated to promoting research to find a cure for polycystic kidney disease (PKD) and improving the care and treatment of those it affects. Our vision is that “no one suffers the full effects of PKD.”

Mission

To promote research to find a cure for PKD and improve the care and treatment of those it affects.

History

The PKD Foundation was established in 1982 by Joseph H. Bruening and Jared J. Grantham, MD, and is headquartered in Kansas City, MO.

Program

Scientific Research, Public Awareness and Patient Education, Government Relations.

Impact

In 2007, the PKD Foundation will fund more than $4.2 million in vital PKD research and lobby the federal government for millions more. In addition to funding research, the PKD Foundation provides a forum for patients, family and friends through more than 70 volunteer-led Chapters across the country and the world and holds the annual Walk for PKD, held each year on the third weekend in September, and the National Convention on PKD, the only conference in the world for PKD patients and medical professionals.

Chief Executive

Dan Larson

Countries of Operation

United States

States of Operation

Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming, American Samoa, Federated States of Micronesia, Guam, Marshall Islands, Northern Mariana Islands, Palau, Puerto Rico, Puerto Rico, U.S. Minor Outlying Islands, Virgin Islands of the U.S.