Welcome to the

Salt Lake City

community

With the help of our communities in cities across the country and beyond, we provide a forum for patients who want to join in the fight to find treatments and cure for PKD.

Connect with us to find out how you can make a difference in the lives of thousands in the U.S. and millions worldwide.

Get Involved

Are you interested in helping us grow the Salt Lake City Community?

We are looking for volunteers to help us offer more opportunities in your local area. If you are interested in this opportunity to volunteer and further our shared vision to #endPKD, please complete our volunteer form and let us know how you would like to get involved. 

If you have questions, please email us at volunteers@pkdcure.org

abbreviated lockup of PKD Connect Conference 2023 (PKDCON 2023) with PKD Foundation logo and illustration of Denver Colorado mountains

Registration for PKD Connect Conference (PKDCON) is open!

PKDCON brings together every part of the PKD community to provide education, research updates, resources, and networking opportunities. In-person and virtual options are available. Learn more and register today.

PKD Foundation Centers of Excellence badge in PKD Foundation purpleThe PKD Foundation is excited to announce Centers of Excellence. If you are looking for the right healthcare providers to help you manage living with PKD, visit our Centers of Excellence page to learn more about this program and to find a Center of Excellence or a Partner Clinic.

Now, as always, the PKD Foundation is committed to our mission of giving hope, advocating for patients, and building a community for all impacted by PKD. We'll continue supporting our community by providing important resources and timely updates on social media. If you have questions or need help navigating this unprecedented health crisis, we are here for you. Email or call (844) PKD-HOPE.

This could be you!

PKD Connect Ambassador

Interested in volunteering in the Salt Lake City Community? Complete our Become a Volunteer form or email volunteers@pkdcure.org.

Lindsay Roper

Walk for PKD Ambassador

In October of 2016 my 2 month old daughter was diagnosed with ARPKD. The PKD Foundation was a great resource for our family as we began learning about the disease and our daughter’s future. I volunteer with the PKD Foundation to bring families together, create hope, and to someday find a CURE. Come walk with us!

Page last updated December 2022

English Spanish