10/20/2026
In 2004, a 13-year-old boy came home with cola-colored urine. His parents, Bonnie and Ed Schneider, were told he had a rare kidney disease called IgA nephropathy, and that there was almost nowhere to turn.
So they built the place that didn't exist. 💙
If you or someone you love has IgAN, you may know that feeling of searching for answers and finding very few. For more than 50 years after IgAN was first discovered, there was no treatment made for it. Families were left to figure it out on their own.
That has changed. Today there are more ways to treat IgAN than ever before, and more people working every day to make sure every patient can reach the care they need.
If you have questions about your options, your nephrologist is a great place to start, and we're here to help you prepare for that conversation.
Our new short film tells the story of how we got here, from a microscope in Paris in 1968 to a kitchen table in New Jersey to a global community of patients, families, doctors, and researchers.
Whether you were diagnosed last week or years ago, whether you're the patient or the one sitting beside them at every appointment: You are not alone. ❤💙
Find support, resources, and community at IgA Nephropathy Foundation
Thank you to Vertex for making this film possible.
Watch it here: https://youtu.be/RvFmD45lG1A?si=lHQOps0Rsf2auFoO