Media and News

Luisa Miniaci-Di Leo, Montreal QC

"In October, two cysts on my left kidney ruptured.  Had it not been for some PKD patients encouraging me, I would never have written this. They suggested I write down my journey because they too have been through this before. They wanted me to educate those who do not understand...

2022 PKD Summit

The PKD Foundation of Canada was proud to host it's second annual Virtual PKD Summit this November! The summit consisted of 4 evenings with educational events catered towards PKD patients and their loved ones, on November 16th, 17th, 23rd and 24th.

November 2022 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.

#GivingTuesday

#GivingTuesday is November 29th 2022! Help give a voice to a widely unknown disease. Donate this #GivingTuesday to the PKD Foundation of Canada, the only national organization solely dedicated to fighting PKD through research, education, advocacy, support and awareness.

October 2022 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.

Voices of PKD: Eric Hampel

"My PKD journey, like many people’s, started when I was 18 with the ultrasound to diagnose whether I had inherited PKD. My Mom’s side of the family had been identified as having PKD since my late grandfather had a stroke in his 20s and passed away in his mid-30s (both...

Voices of PKD: Kelly Konieczny, AB

"Hello, my name is Kelly Konieczny. I am a daughter, sister, auntie, wife and mother in my family and a friend to many. I live in a small farming community in Alberta and am currently on medical leave from an Educational Assistant position I held for 25 years. This is...

August 2022 PKD e-News

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

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