Each year, approximately 100 advocates from the National Kidney Foundation and allied patient organizations arrive on Capitol Hill to advocate for kidney patients. This year, advocates from the Alport Syndrome Foundation, American Association of Kidney Patients, Nephcure Kidney International, and PKD Foundation will join our members to meet with their Senators and Representatives.
Our advocates will educate their legislators about chronic kidney disease (CKD), and build support for legislation to promote early detection and treatment of CKD (H.R. 3867), the Living Donor Protection Act (H.R. 1270), and appropriations funding for kidney disease programs and research.
Help us make a bigger splash on Capitol Hill!
Please write and tweet to your legislators to support your patient advocates in D.C. Show your legislators that there are thousands of Americans who believe more progress on CKD is needed.
Thank you for your support and please share this email with your friends and family!
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