Rare Kidney Diseases: Challenges, Opportunities, and Alport Patient and Family Perspectives

Living with a rare kidney disease can be isolating and difficult. Join us for a frank discussion about the challenges involved in researching rare diseases, the changing landscape in this space, and some exciting new developments on the horizon in Alport research. Hear from patients and families navigating Alport Syndrome and learn more about their experiences living with this disease. Don’t miss this unique opportunity to better understand rare kidney diseases and get to know others in the community!

Speakers: Dr. Moumita Barua, Lisa Bonebrake, Liz Pederson, Thierry Klesse

In collaboration with the Alport Syndrome Foundation

The Kidney Foundation would like to thank our sponsors for making the 2024 Kidney Foundation Webinar Series possible.