Meet Nick Ashawasega

Credit: PKD Foundation of Canada

“I was five years old when I first noticed the blood in my urine. Polycystic kidney disease. My family had no idea what that diagnosis meant, no idea what we were supposed to do. There was no playbook for raising a young indigenous child with PKD.”

What’s your story?

Listen to Nick’s PKD story here, then read the rest:
https://www.patientvoice.io/shorts/li…