YOU DESERVE EQUAL ACCESS TO KIDNEY TRANSPLANTS
Although a kidney transplant is not a cure for kidney failure, it is considered the best treatment for it. Generally, people who have successful kidney transplants often enjoy a better quality of life than what is possible on dialysis.
The truth about kidney transplant access in America
Even though Black and Hispanic/Latino Americans are more likely than white Americans to develop kidney failure, also called end-stage renal disease (ESRD) or end-stage kidney disease (ESKD), they are often on the kidney transplant waitlist the longest.
- Black Americans are about 25% less likely to be placed on the kidney transplant list than white patients.
- Once on the list, Black patients often wait more than three years for a kidney, compared with about two years for white patients.
- Hispanic/Latino patients also face delays, often waiting months to years longer than white patients for a deceased donor kidney.
- Based on a University of California Irvine study, Hispanic patients are less likely to receive a kidney from a living organ donor than white patients.
- Although Black people make up about one-third of those on the waitlist, they receive only about 14% of living donor kidney transplants.

2025 AKF Living Donor Protection Report Card
Where Americans live can affect their ability to give the gift of life
AKF's State of the States: 2025 Living Donor Protection Report Card evaluates each state and the District of Columbia on how well their existing laws encourage living organ donation and reduce barriers for living donors.
Access to kidney transplant
Reasons for differences in Kidney Transplant
Medical bias
Some medical rules and tests have made it harder for people of color to be referred for a transplant.

- eGFR calculations: For many years, kidney function tests (eGFR or estimated glomerular filtration rate) included race, which made Black patients' kidneys look healthier than they were. This delayed referrals to kidney doctors for thousands of people. Since 2021, race is no longer used in eGFR calculations.
- BMI limits: Some programs use strict body-mass index (BMI) cut-offs, even when weight alone may not predict the success of a transplant.
- Other assumptions: Health care professionals may make decisions based on genetics or outdated rules instead of a person's overall health and support system.
- Immunologic compatibility testing bias: Tests used to match organs are often based on genetic information from mostly white donors. This makes it harder for people of color to find a close match and can cause longer wait times for a kidney transplant.
Implicit bias
Implicit bias are thoughts or feelings about people you don't realize you have. Hidden feelings, beliefs or stereotypes can affect how health care professionals talk about transplant and which patients they refer to a kidney doctor. These biases can lead to fewer referrals and slower progress for people of color. Examples include:
- Assuming some patients won't be able to take medicines on time or keep follow-up visits after surgery
- Believing people from certain communities won't have enough support at home to manage recovery
- Spending less time explaining transplant options or answering questions for patients of color
- Expecting worse results based on race or ethnicity rather than looking at a person's health and support system
Financial barriers
Finances often influence who is referred, evaluated and able to stay on a transplant list.
- Limited or no health insurance may keep people from seeing a specialist or getting listed
- Out-of-pocket costs, including travel, lodging, or lost wages, can discourage evaluation
- Some people worry they cannot afford the medicines needed after a transplant
Systemic barriers
Access to transplant care depends on more than medical need. Structural issues, such as the location of transplant centers, housing, transportation, and language support, can make it harder for Black, Hispanic/Latino, and other minority patients to get timely evaluations. None of these challenges should stop you from seeking a transplant. With the right support and information, you can take the steps needed to be evaluated and move toward a kidney transplant.
How to improve your chances of receiving a kidney transplant
One of the best things you can do to improve your chances of a kidney transplant is to plan ahead. If you have kidney disease, it is possible you may never have kidney failure. But because transplants are a complex process, it is a good idea to prepare in case you experience kidney failure.
Learn about the transplant process: The first step is to learn as much as you can about how kidney transplants work, including preemptive transplants (getting a transplant before starting dialysis) and living donor transplants. Tell your doctor you want to know what you need to do to get a kidney transplant.
Learn about the waitlist: Once you are in Stage 4 chronic kidney disease (CKD), work to get on the waiting list. The first step is to ask your kidney doctor (nephrologist) for a referral to a transplant center for a transplant evaluation. If your doctor says no, get a second opinion
Get an estimate for kidney transplant wait: The Scientific Registry of Transplant Recipients (SRTR) Kidney Transplant Waiting Times tool shows how long people with health experiences similar to yours have typically waited for a deceased donor kidney. The estimates are based on 2024 data and include time on the waitlist, whether active or inactive. They're not exact predictions, but it can give you a better picture of what to expect.
Speak up for yourself: Doctors sometimes think their patients are not eligible when they really are. The transplant center does the evaluation, not your kidney doctor or regular doctor, so keep advocating for yourself. If the evaluation finds that you are not eligible, find out what you need to do to become eligible. You can also list at more than one transplant center, and eligibility requirements can vary from one center to another, which may improve your chances of being listed.

Spread the word about living kidney donations
Another way to shorten your wait is to talk with your family and friends about living kidney donation. Tell them you may need a kidney transplant eventually and that you want to start preparing. Share all the information you have and tell them you don’t need a kidney right now, but want to start thinking about it early. You may have a family member or friend who is willing to give you the gift of life by becoming a kidney donor.

Resources
Resources and tools
Learn about preventing and managing kidney disease.
- Talk to Your Doctor Guide
- Home Dialysis Decision Aid
- Talk with your patients about home dialysis: Learn the OARS technique
- Your guide to kidney transplants
- Post transplant toolkit
- Genes to Generation: Know your family’s health history
- Talk With Your Patient about Clinical Trials
- Talk To Your Doctor about Clinical Trials
- Organ and Tissue Donation Myths Debunked
Get involved and join the fight
Join AKF's movement for kidney health equity. Learn how to become a Kidney Health Coach, apply for grants, partner with us, train as an advocate, or share your story to help prevent kidney disease and support communities.
