News and Information
What can we do for you?
The Seattle Chapter wants to hear from YOU! Please take our SURVEY and let us know what programs interest you the most.
I look forward to hearing from you!
Seattle Chapter Coordinator
Hello, my name is Lara Macklin and I am excited you stopped by! As your Seattle area Chapter Coordinator I would like to thank you for taking the time to visit our site as this is where your local connection to the PKD Foundation begins. We are here to educate, inspire and support your efforts in managing PKD by connecting with others in the area, to learn about similar experiences, local resources and success stories. I can almost guarantee you will make some new friends as well! We are passionately dedicated to helping the Foundation find treatments, and ultimately a cure for PKD, so that no one has to suffer the full effects of this disease. There is also an on-line support group site to allow for open conversations about PKD, ask questions and share thoughts with other Seattle locals. The site will be moderated and all posts should be relevant to PKD. If you would like to join this group please click on the link below and subscribe. We look forward to "meeting you" on-line!
Thanks to Northwest Kidney Centers! NKC is a major supporter fo the Seattle Chapter. They always have a team at the Walk for PKD and invite us to their many events. While we all hope to never need their dialysis service, it sure is nice to know they're there AND will take good care of us! Thanks NKC!
Registration for fall Walks is now open. With more than 50 Walks across the country and the Virtual Walk, we can all unite to fight PKD.
We had an amazing time at the Transplant Games of America! Thank you to everyone that stopped by our booth and shared your transplant story with us. Congratulations to everyone that participated in the games!
Local Events and Meetings
The Seattle Chapter generally meets the first Saturday of each month. For more information, please email Lara at email@example.com.
Seattle Walk for PKD
Sunday, October 26
For more information, click here!
Presented by Neera Dahl, M.D., Ph.D., Assistant Professor of Medicine (Nephrology) at the Yale School of Medicine
Join us for an interactive discussion about PKD including a general overview of both ADPKD and ARPKD, common symptoms and frequently asked questions. Great for newly diagnosed patients as well as those who want to support a friend or family member with PKD.
PKD Discussion forums provide a place for patients, family and friends to make connections, ask questions and share stories and experiences.