Welcome to the NKF Action Center

The National Kidney Foundation (NKF) is the largest, most comprehensive and longstanding, patient centric organization dedicated to the awareness, prevention and treatment of kidney disease in the US. Together, we can enhance the lives of kidney patients by making our voices heard in support of the issues affecting funding, treatment, research and more. Join the effort today.

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Use Your Voice to Help Kidney Disease Patients

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Tell Congress to Act to Fund Kidney Disease Research and Programs! The latest data coming from CDC’s Chronic Kidney Disease Surveillance Project shows the number of Americans with CKD is higher than previously estimated. There is action Congress can take to support funding for research and programs that generate awareness and promote improved access to treatment for CKD.

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The Living Donor Protection Act will protect living organ donors and remove barriers to donation by prohibiting insurance companies from denying or limiting life, disability and long term care insurance to living donors, and from charging higher premiums.  It will also help to protect the jobs of living donors while they recover from donation.

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Tell your story and urge your U.S. Representative and Senators to reintroduce and sponsor the Living Donor Protection Act, provide lifetime access for immunosuppressive medications through Medicare, and create a demonstration program to improve early detection and management of chronic kidney disease (CKD).

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2016-summit

On March 7th, 150 advocates for the National Kidney Foundation, Alport Syndrome Foundation, American Association of Kidney Patients, Home Dialyzors United, Nephcure Kidney International, and Polycystic Kidney Disease Foundation will meet with their Representatives and Senators in Washington, DC to bring chronic kidney disease (CKD) to the forefront of health care policy discussion.

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Have end-stage renal disease (ESRD)

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Americans on the Kidney Transplant Waitlist

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People with ESRD who died in 2014

You are the strongest advocate for kidney disease patients, living donors, and their families

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