Portland ChapterConnect. Support. Educate.

With the help of PKD Foundation Chapters in cities across the country and beyond, the PKD Foundation provides a forum for patients who want to join in the fight to find a treatment and cure for PKD. Just contact us at portlandchapter@pkdcure.org to find out how you can make a difference in the lives of thousands in the U.S. and millions worldwide.


 News and Information News and Information

Thank you for joining us at the Portland Walk for PKD!

The Walk may be over but fundraising will remain open until Dec. 31. Click the button below to make a donation to the Portland Walk today!

 Donate today!

What can we do for you?

The Portland Chapter is here for YOU! Our Volunteer Coordinators plan education, support and fundraising events to support PKD families in the Portland area and to support the Mission of the PKD Foundation. It is very important to us to know how we can be of service to you and your family. Please connect with us if there is anything we can do for you. YOU are always welcome!

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PKD Patient Handbook

June 2015

The newly updated PKD handbook is now available! The revised handbook has undergone extensive reviews and updating by PKD experts. Topics include PKD signs and symptoms, diet and nutrition, kidney failure, transplantation and more.

Download your digital copy today!


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Calendar Local Events and Meetings

Meeting Chapter Meetings 

Chapter meetings are another opportunity for you to have your questions and concerns about PKD addressed. We will do our best to provide you with answers or direct you to someone that can assist you. Everyone is welcome! 

We do not have any meetings scheduled at this time but we would still like to hear from you. If you have any questions concerning support meetings, please email our Volunteer Chapter Coordinator Alex at portlandchapter@pkdcure.org.   

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 Portland Walk for PKD

Walk for PKD    


Thank you to all who joined us for the Portland Walk for PKD!

 We had a great time! Check out some of our favorite memories from the Walk here.



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Resources Resources

Sign Up to Receive Information From Your Chapter

Next Webinar Wednesday

Webinar Wednesdays with CSO David Baron, Ph.D.Genetics of PKD

Wednesday, Nov. 18, 12 - 1 p.m. CDT

PKD Foundation Chief Scientific Officer David Baron, Ph.D., will explain the genetics of ADPKD and ARPKD. He will include a overview of some of the genetic research currently being conducted.


Next Free National Webinar

Dr. David BaronThe sequence of drug development

Wednesday, Dec. 2, 2015, 7 to 8 p.m. CST

Presented by: David Baron, Ph.D., PKD Foundation CSO

Why does a drug therapy take so long to find? Hear from PKD Foundation Chief Scientific Officer David Baron, Ph.D. as he uses his decades of experience in drug development to explain the process as it relates to PKD. Also included will be a discussion of clinical trials – why they are important and how to find out about them.

Register now

Watch previous webinars here.


PKD Connection

Discussion Forums

PKD Discussion ForumsPKD Discussion forums provide a place for patients, family and friends to make connections, ask questions and share stories and experiences.

Join the Conversation

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Your Organization

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©2015, PKD Foundation ·The PKD Foundation is a 501 (c)(3), 509 (a)(1) public charity.

©2015, PKD Foundation ·The PKD Foundation is a 501 (c)(3), 509 (a)(1) public charity.