Kidney Today Blog

AKF new Board of Trustee member, Lydia Landesberg, shares how her family came together to support each other after they discovered several family members had a ...

On Sept. 21, AKF hosted its first Rare Kidney Disease Advocacy Day on Capitol Hill, connecting patient advocates from the IgAN Foundation, health care professio...

Sept. 4 is Polycystic Kidney Disease (PKD) Awareness Day, and while it is the most common form of genetic kidney disease, you may not know much about it. Here a...

In this guest post, IgAN Foundation ambassador Michelle Minkoff Carlson shares lifestyle changes she made to manage her IgA nephropathy and protect her transpla...

Find out about six provisions in the New Era for Preventing End-Stage Kidney Disease Act that will help people with rare kidney diseases.

Employees at Heart+Mind Strategies participated in a fitness challenge to fundraise for a charity of the winners' choosing. We were delighted when Marjie S...

Living with a rare disease that few people know about or understand can be challenging. Get tips on making your voice heard.