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Susan, AB | Voices of PKD

"Hello, my name is Susan. My journey with PKD began in my 20’s, when I was told I had a few cysts on my kidneys. I was told that having a few cysts was not unusual, and not to be concerned."

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December 2015 PKD e-News

Support    There’s Still Time to Make Your Year-End Gift!  With 2015 drawing to an end, we wish to express our heartfelt thanks to you, our donors, for helping to make this another memorable year for the PKD community.

October 2015 PKD e-News

Awareness  PKD Foundation of Canada Holds First-Ever PKD Advocacy Day at Queen’s Park As part of our ongoing advocacy activities, the PKD Foundation of Canada held their first-ever PKD Advocacy Day at Queen’s Park on Wednesday, October 7th. Our Executive Director, Jeff Robertson was joined by Board Chair, Joseph Brant...

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