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Blog

Courtney Gibson, ON | Patient Story

"Hi, my name is Courtney Gibson. I’m 28 years old, and this is the story of how a complete stranger gave me a second chance at life. When I was born, doctors told my parents I would never walk, talk, or sit up on my own...

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Kim Holowatiuk, AB | Voices of PKD

"Living with Stage 5 polycystic kidney disease (PKD), I’ve experienced a huge loss of muscle mass, balance, and strength. The fatigue alone has been incredibly discouraging. I used to be very active—even an athlete—so feeling so limited now has been frustrating and disheartening."

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PKD Awareness Day 2025

Let's get lit up for PKD Awareness Day 2025. Here you'll find information about landmark lightings, flag-raisings and how to get involved!

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News

Monthly News

News

March 2024 issue | PKD e-News

In our e-News this month: March is Kidney Health Month! Voices of PKD from Karen; Kidney Nutrition: making substitutions in recipes for PKD; upcoming PKD nutrition webinars in English and French; upcoming webinar on PKD and mental health; new resources for having conversations about PKD.

February 2024 issue | PKD e-News

Welcome to the February e-News from the PKD Foundation of Canada! You'll find useful information to help you take steps in dealing with polycystic kidney disease.

January 2024 issue | PKD e-News

Welcome to the January e-News from the PKD Foundation of Canada! You'll find useful information to help you take steps in dealing with polycystic kidney disease.

December 2023 issue | PKD e-News

Welcome to the PKD Foundation of Canada's December e-News! We have provided information important to helping you take action in your journey with PKD.

November 2023 issue | PKD e-News

Welcome to the PKD Foundation of Canada's November e-News! We have provided information important to helping you take action in your journey with PKD.

October 2023 issue | PKD e-News

Welcome to the PKD Foundation of Canada's October e-News! We have provided information important to helping you take action in your journey with PKD.