ADPKD is the most common inherited renal disorder worldwide, impacting approximately 1 in every 500 Canadians. An estimated 45% to 70% of patients with ADPKD progress to end-stage renal disease by age 65 years.
"Hailey-Ann is a vivacious, four-and-a-half-year-old girl who loves life. When I was only 21-weeks pregnant with her, my pregnancy went from one of joy and wonder, to one of fear and uncertainty. That is because at my 21-week ultrasound with our high-risk team, they discovered that my unborn child would...
With 2018 drawing to a close, we hope you remember the PKD Foundation of Canada in your holiday plans and consider making a year-end gift to help advance Canadian research, advocacy and support for PKD Warriors like Hailey-Ann, and their families.
This past September, the University Health Network held a two-day PKD Scientific Conference to: Highlight recent research advances in PKD; Illustrate how this knowledge is being translated into improving risk prognostication and novel therapeutics in PKD; and Provide practical guidance on risk assessment and clinical management of PKD through interactive...
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.
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.
Welcome to the PKD Foundation of Canada's September e-News! We have provided information important to helping you take action in your journey with PKD.
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.
On April 18, 2018 we held the Quebec City PKD Patient Forum at the Château Bonne Entente with Université Laval Nephrologist Dr. Paul René de Cotret and PKD Foundation of Canada Executive Director Jeff Robertson.
Are you ready to take on the challenge? Help spread the word about PKD Awareness Day and what it's like to live with polycystic kidney disease! Record a short video with your smartphone and tell us your story...