Welcome to the
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.
Walk Volunteer Needed!
We are in search of a key volunteer to lead efforts for the Nebraska Walk for PKD. This volunteer leader role is vacant and the continued success of the Nebraska Walk for PKD relies on leadership in this role and in your area. If you are interested in this opportunity to volunteer and further our shared vision to #endPKD, please reach out.
Email us at email@example.com with the subject line: Nebraska Walk Volunteer Interest and we would be happy to talk with you!
Are you interested in helping us grow the Nebraska 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 firstname.lastname@example.org.
The 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.
If you’re looking for a shoulder to lean on or want to help others from the safety of your home, our Peer Mentor Program is a great resource:
PKD Connect Ambassador
I live in Omaha with my two daughters. I learned about PKD 15 years ago when my father was diagnosed. My focus will be on PKD advocacy, and will keep the chapter informed of important legislation.
Page last updated December 2022