Living with PKD can be both emotionally and physically difficult. Knowing you are not alone can have a positive impact on your condition. Connecting with others who are going through a similar experience can give you the confidence to better manage your PKD.
Whether you’re sharing your story, listening to someone else’s, or catching up on the latest scientific breakthroughs in the understanding of PKD, being part of a community can be inspiring and healing. Get connected today, and explore some resources and patient-focused organizations within the PKD community.
This is not an exhaustive list. Please note that Otsuka does not control or influence any of these websites.
Foundations and informative sites
Education and advocacy for kidney patients in the United States
Provides charitable assistance to dialysis patients who need help with the costs of treating kidney failure
A service of the US National Library of Medicine, with information on over 900 diseases
Peer support and information for kidney patients
Dedicated to PKD research and education
Global alliance of patient organizations worldwide, dedicated to finding a cure and offering disease education for PKD