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Voices of PKD

Voices of PKD is a collection of testimonials and photos that tell the story of PKD through the eyes of the PKD community.

You can help give a voice to a widely unknown disease by sharing your story. Your experiences can paint a powerful picture of what it’s like to live with PKD.

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Featured Voice

PKD

Angela Pickard and Bradley Stewart, Chatham ON | Voices of PKD

"I was born in 1974 and diagnosed with autosomal recessive polycystic kidney disease (ARPKD) shortly after birth. My life expectancy was only a few years."