About Us
With more than 35,000 members from every state in the country, Dialysis Patient Citizens (DPC) is working to improve the quality of life for all dialysis patients through education and advocacy. We are the largest nationwide, non-profit, patient-led organization with membership open to dialysis and pre-dialysis patients, transplant recipients, and family members. Our mission and policy priorities are guided solely by our membership and Board of Directors, which is comprised entirely of dialysis patients and kidney transplant recipients.
DPC also has a robust partners-in-care program, uniting dedicated kidney health care professionals who share DPC’s mission of promoting patient empowerment and quality kidney care for all.
Mission and Charter
Dialysis Patient Citizens is a patient-led, non-profit organization dedicated to improving dialysis citizens’ quality of life by advocating for favorable public policy.
Vision
To ensure optimal dialysis care through continual improvement of public policy.
DPC wants to give a voice to dialysis patients.
One of DPC’s goals is to provide dialysis patients with the education, access and confidence to be their own advocates. Through our grassroots advocacy campaigns, Patient Ambassador program; Washington, DC patient fly-ins; conference calls and briefings, DPC works to train effective advocates for dialysis related issues. DPC is here to rally patients to have their voices heard.
Patient-Led Organization
The intent of DPC is to reflect the voice of the patients. Our Board of Directors is composed of people with end-stage renal disease. We also rely on input from our membership to determine both our education and advocacy priorities. DPC members are invited to complete education and advocacy surveys to help shape DPC’s focus and determine the organization’s priorities.