Voices of PKD is a collection of testimonials and photos that tell the story of PKD through the eyes of the PKD community.
You can help give a voice to a widely unknown disease by sharing your story. Your experiences can paint a powerful picture of what it’s like to live with PKD.
"I was 42 when I found out I had polycystic kidney disease. Until that day, I’d never even heard of PKD. There wasn’t much information available to me at the time, either. What I understood was fairly simple: eventually, I might lose kidney function. Beyond that, I didn’t really know what living with PKD would mean."