PKD: When it comes to a hereditary disease you have no say in it | Green Table Talk

Jennen is joined by Judith and Luisa who live with polycystic kidney disease (PKD). In this episode both women talk about the long road to diagnosis, the importance of self-advocacy, looking for a living donor and working with the PKD community and others across Canada and around the world to raise awareness, improve care and find a cure. For more information about PKD visit To hear more about Luisa's journey and work as PKD Foundation Montreal Chapter lead, watch this episode of Bobby's Short Shorts To connect with Judith check out her blog: (en francais) or Facebook page: (bilingual) For information about the paired kidney donation program visit If you would like to explore living donation or become a non-directed anonymous donor visit