The National Kidney Foundation has launched a new patient advocacy and engagement program to expand its grassroots network at the state level. The Kidney Action Committee is comprised of 60 patient liaisons, including one from each state, who are personally affected by kidney disease. These individuals will use their experience to advise government agencies, research organizations, and policy and health organizations on kidney disease.
They will also provide input on the development of NKF public policy positions and the implementation of kidney disease education programs.This new program builds upon NKF’s Advocacy Action Center —a group of over 60,000 people who advocate on behalf of kidney patients.
“We’re strengthening our national advocacy presence by expanding our multi-state efforts,” said Kevin Longino interim Executive Officer of the National Kidney Foundation. “These 60 individuals will be the face of NKF at the state level. It’s an important role, but we have very dedicated volunteers who are passionate about making sure the needs of kidney patients are addressed.”
Members of the Kidney Action Committee will promote NKF priorities locally and nationally through media interviews, visits with lawmakers, and special events.
“As someone affected by kidney disease, I know how crucial advocacy and engagement is to furthering our cause,” said Alexandra Harrison, a newly-elected patient liaison. “I’m looking forward to creating local momentum behind the key issues that will make a positive difference for kidney patients in California and across the country.”