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"My name is Karen, and this story is about my journey with polycystic kidney disease (PKD). I was diagnosed at the age of 18. I knew it was a condition that not only threatened my own health, but also had the potential to be passed...
Read moreDo you talk about PKD within your family, or are those conversations that you try to avoid? In this blog, we explore the intricacies of planning for important family conversations about PKD, so that you can turn apprehension into unity, mutual support and informed decision-making.
Read moreIntroducing our new patient education resource: Having a Conversation with Your Adult Children about Your PKD Diagnosis. This comprehensive, printable PDF includes a wealth of content that we hope you will find helpful in having conversations about PKD.
Read moreWe are so excited that our Board of Directors has selected Kathleen Barnard as our new Executive Director! Kathleen is a seasoned, community-focused senior executive with nearly 20 years of experience leading strategic initiatives and programs for nonprofit organizations.
Read moreWelcome to the PKD Foundation of Canada's November e-News! We have provided information important to helping you take action in...
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Welcome to the PKD Foundation of Canada's September e-News! We...
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