Don’t rule me out
Tell Congress that kidney patients have the same right as anyone to choose private insurance coverage.
Thirty-one million Americans are living with chronic kidney disease, including more than 650,000 individuals who have kidney failure and rely on dialysis or transplantation to survive. As the nation’s largest nonprofit organization serving people with, and at-risk for, kidney disease, the American Kidney Fund is a strong and independent voice to increase awareness of kidney disease and advocate for policies that improve access to health care and that strengthen quality of care for individuals with kidney disease. We work with Congress, the administration, federal agencies, and state governments to advance legislation and regulatory policies important to kidney patients and their families.
Our Advocacy Network plays a vital role in influencing public policy that helps ensure access to quality care for kidney patients, as well as educating communities about kidney disease, its causes, and how to prevent it. Learn more about advocacy and how you can make your voice heard.
Keeping policymakers informed is critical in the fight against kidney disease. Add your voice to thousands of other voices in our Advocacy Network and help us make a difference!
There is strength in numbers. More than 5,100 passionate patients, friends, loved ones and kidney care professionals in our Advocacy Network are making a huge difference on Capitol Hill and in their own communities. Together, we are fighting for policies that help patients. Add your voice to our Advocacy Network by joining today.
In the ongoing debate over third-party premium payments, it is easy to lose sight of the most important aspect: the patient. When AKF is unable to help low-income kidney patients to maintain their insurance coverage, the effect on patients can be devastating. Learn more about our position.
Decisions made by Congress and government agencies affect the quality of care that dialysis patients receive, the amount funding for kidney disease research and the payment of health care providers. We continuously monitor regulations and legislation that affect kidney patients and their families, and—together with like-minded organizations and our Advocacy Network—we work with Congress, the administration, federal agencies, and state governments to advance our legislative and regulatory policy agenda. Read about the issues we are monitoring and working on this year.