Below you'll find a list of all posts that have been tagged as “National Kidney Registry”
By Martha Gershun, Guest Blogger As a living kidney donor, I often hear from people who have recently been diagnosed with End Stage Renal Disease (ESRD) or have a relative who is a kidney patient. These patients have usually been given little information about the advantages of living kidney donation and almost no guidance on how to maximize their chances of finding a donor. Many providers, who are highly experienced in the medical and surgical …
Written by Martha Gershun, Guest Blogger A bipartisan Congressional leadership team from both houses introduced new federal legislation on April 27 designed to protect living organ donors and promote organ donation. The Living Donor Protection Act (H.R. 2923) was introduced by Congressman Jerrold Nadler (D-NY), Congressman Troy Balderson (R-OH), Congresswoman Lisa Blunt Rochester (D-DE), Congressman Jim Costa (D-CA), Congressman John Curtis (R-UT), Congresswoman Diana DeGette (D-CO), Congresswoman Mariannette Miller-Meeks (R-IA), Congressman Gregory F. Murphy, M.D. (R-NC), …
By Rachyl Pines, PhD, Postdoctoral Fellow Dr. Waterman and Dr. Pines are the research committee leads for the National Kidney Registry (NKR), a non-profit organization whose mission is to “save and improve the lives of people facing kidney failure by increasing the quality, speed and number of living donor transplants in the world as well as protecting all living kidney donors.” Learn more about this organization by clicking here. The NKR has been a leader …
It’s one of the frustrations of the kidney shortage that many people want to donate a kidney to a loved one but can’t, because their blood type is not compatible with their intended recipient. If they donated, their kidney would be rejected. In the past, living donors who did not match their recipients simply couldn’t donate at all. The failure to realize those donations was – and is – a true loss of potential kidneys …