Our 2025 virtual PKD Patient Forum for Atlantic Canada featured a regional nephrologist sharing information and answering questions about Jinarc / tolvaptan for ADPKD, along with a regional PKD patient sharing the story of her personal journey with ADPKD and tolvaptan.
Watch this special roundtable discussion with Dr. Matthew Lanktree, Nephrologist, and Nick Ashawasega, ADPKD patient, where we explore the basics of genetic counselling and testing for PKD.
This month we have information on the 2025 Walk to END PKD season, this year's PKD Summit registration, food safety for the immunocompromised, and more!
For many people with PKD, the emotional side of the disease may be as challenging, and sometimes more, when compared to the physical side. Dr. Gavril Hercz brings a rare perspective as both a kidney specialist and psychotherapist.
This Diverticulitis Disease Awareness Week (U.K.), we’re raising awareness about the link between gut and kidney health in people with ADPKD.
Important message: A possible Canada Post disruption may delay mailed donations and receipts. To ensure your support reaches us without delay, please donate online at endPKD.ca/donate. Your gift matters now more than ever.
Food safety means handling, cooking, and storing food so it doesn’t make you sick. It matters for everyone - especially people with PKD and transplant recipients - because it lowers the risk of food poisoning. Here’s what it involves and why it’s important.
This month we have information about the Walk to END PKD, PKD nutrition when life gets busy, 50/50 raffles in Ontario and Nova Scotia, and more!
You've just been diagnosed with polycystic kidney disease (PKD). What happens next? Do the words hit hard, stirring up shock or fear? Does everything now make sense? Whatever the feelings, you're not alone.
This is a love letter to someone with PKD. (Maybe you.)