PKD International
We are a global alliance of patient organizations dedicated to a cure for Polycystic Kidney Disease (PKD).
Our mission is to improve the lives of an estimated 12.5 million affected by PKD worldwide, and their families and care-givers. We will do this by uniting patients, families, scientists, and healthcare professionals committed to ending PKD.
Support our European PKD Awareness and Fundraising Campaign
PKD International is a non-profit, non-governmental association (NGO) based in Geneva, Switzerland.
PKD Patient Groups, individuals and clinicians, scientists and other healthcare professionals worldwide are invited to join PKD International.
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Volunteers needed for ADPKD pediatric clinical trial
8 August 2017Volunteers are needed to participate in a clinical research trial for Pediatric Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD).
Posted In: Research -
ADPKD Controversies Conference Report published
25 April 2015KDIGO Controversies Conference Report on ADPKD has been published.
Posted In: International, KDIGO -
European ADPKD Forum Report Launched
29 January 2015Launch of the EAF Report on Autosomal Dominant Polycystic Kidney Disease (ADPKD).
Posted In: Europe -
Expert group formed to improve the management of ADPKD throughout Europe
31 May 2014A new multidisciplinary group of leading medical and patient group experts was formed.
Posted In: Europe -
KDIGO Controversies Conference held on ADPKD
26 January 2014The first-ever Controversies Conference organised by KDIGO on ADPKD was held in Edinburgh
Posted In: KDIGO -
Raising awareness of PKD across Europe
17 March 2013Leading patient groups join forces on World Kidney Day in a new drive to tackle an important yet neglected genetic kidney disease.
Posted In: Europe
