
Stephanie
IgAN, Rare LifeIn the spring of 2020, after a hike with her husband and kids, Stephanie’s legs swelled unfathomably. She took a video of herself pressing her fingers into her legs, showing how her fingers would sink into the skin.

Stuart
IgAN, Rare LifeTen years after being diagnosed with IgA nephropathy, a rare kidney disease, Stuart’s kidney function had depleted significantly. Today, after a lifesaving kidney donation from his wife, Stuart gives back to the kidney community through advocacy

Gisela
IgAN, Rare Life“How do you know you have IgA nephropathy?” asked Gisela’s nephrologist skeptically. Gisela was 30 years old, talking to a nephrologist for the first time in a decade. Read and watch her story.

Lillie
IgAN, Rare LifeLillie – living with IgA nephropathy, and her mom Carrie, talk about life with rare kidney disease.