Kidney Today Blog

In honor of PKD Awareness Day, Mary Biafra Denmark shares how she learned she had the genetic mutation for PKD

An overview of five treatments for kidney disease recently approved by the FDA

AKF Ambassador Ariana Barton shares her journey living with IgA nephropathy, a rare kidney disease

A Q&A with Alonzo Mourning about APOL1-mediated kidney disease

As part of our 2024 Kidney Action Week™ (KAW), AKF's Office of Government Affairs hosted three sessions on March 19, KAW's Community Action Day.

To help spread awareness for people living with the rare genetic disease and for people who may be at risk, here are 10 facts about Alport syndrome.

February 28 (or for Leap Year, February 29) is Rare Disease Day, a day recognized across the globe that is dedicated to spreading awareness of the 300 million p...

As we count down the days until the start of the American Kidney Fund's fifth annual Kidney Action Week, we are previewing a few of the exciting sessions t...

We are so proud of the impact AKF made in 2023 on the lives of people with kidney disease, who are at the heart of everything we do. In 2024, as always, people ...