Below are a number of resources about the 2025 KDIGO ADPKD Guideline.

2025 KDIGO ADPKD Guideline | Webinar

The video recording from our March 26, 2025 webinar - a discussion between Canadian nephrologist Dr. Matt Lanktree, and PKD Foundation of Canada board member and ADPKD patient Henry Osei-Agyekum - is now available to view anytime on our YouTube channel.

You can find the downloads page for the 2025 KDIGO ADPKD Guideline here.

You may not want to read the entire 900-page guideline... but you might enjoy the 10 one-page infographics and summaries of each chapter.

They can be found on the same downloads page as the full guideline.

Dr. Lanktree and Henry didn't use a slide deck for their roundtable, but we prepared one, if you would find that helpful.

The slide deck is organized by guideline chapters, with common questions that patients ask us about each topic.

Throughout the month of March 2025 we shared daily blogs on the individual chapters of the KDIGO ADPKD Guideline.

Topics included:

• Overview of ADPKD
• PKD Genetics
• Early Signs of PKD
• PKD Stages and Labs
• Individual Prognosis
• Hypertension
• Cysts and Kidney Stones
• Polycystic Liver Disease
• Nutrition
• Tolvaptan

You can find all of the blogs on our new online PKD community, My PKD.

If you're already a member of My PKD, login and click the button to find the master list of March blogs.

Click the button to request to join My PKD today!

Patients, family, friends, organ donors and healthcare providers are all welcome on our free, private, and confidential community platform.

Thank you to everyone who completed a survey after the event - your feedback is important to us. We want to present events that will be valuable for the PKD community.

Feel free to reach out anytime to share further questions or feedback with us.

Did you know that resources like our learning events, peer support and our online PKD community, My PKD, are only made possible through donations and funding?

Your gift helps connect patients and families with the resources they need. Please consider making a donation today.

Working for a cure,

Your friends at the PKD Foundation of Canada

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