We are pleased to share some encouraging news regarding the treatment landscape for those living with ADPKD. Today, Otsuka announced results from their Phase 3 REPRISE trial of tolvaptan in patients with autosomal dominant polycystic kidney disease (ADPKD). This data was presented at the American Society of Nephrology (ASN) Conference...
Since 2007, the PKD Foundation of Canada has raised over $1M for critical PKD research, education, advocacy and awareness through our Walk to END PKD campaign! Truly an amazing feat for our grassroots organization.
Registration is open for the 2017 Walk to END PKD, the PKD Foundation of Canada's signature fundraising campaign.
We are thrilled to introduce the new name and new look for our signature fundraising event! The new name, Walk to END PKD (formerly Walk for PKD), better aligns with our mission to discover treatments and a cure for polycystic kidney disease and improve the lives of all it affects....
We are glad to share some great news for the Canadian PKD community, as tolvaptan receives positive results from an additional one year international trial. The trial outcome was positive for tolvaptan in the treatment of ADPKD. Also of note, the trial had participation from Canadian patients and nephrologists.
We’re very excited to share the pilot episode of our brand new PKD podcast, PKD Talks.
The PKD Foundation of Canada is pleased to share that a Canadian consensus has been published by nephrologists across the country. This consensus aims to give nephrologists evidence-informed recommendations to guide optimal management of adult patients with autosomal dominant polycystic kidney disease (ADPKD).
We have upcoming Polycystic Kidney Disease (PKD) Patient Forums in Winnipeg and Saskatoon! Join us to learn more about what a PKD diagnosis can mean for you or a loved one, how it can be managed and what resources and support systems are available. Our Executive Director, Jeff Robertson, and...
The fourth and final article in our National Post PKD series features Jan Robertson, a woman who is seeing new hope after years of living with polycystic kidney disease. Doctors discovered Jan had PKD more than 35 years ago, and she hasn’t stopped fighting since. Read more about Jan’s story, and...
Part three of our four-part National Post PKD series features a Nova Scotian woman, now living in Toronto, ON. Jil Eisnor was 20 years old when she discovered she had polycystic kidney disease, but she hasn’t let it stop her from living a normal life. Jil has the mutated gene, meaning...