News and Information
Welcome to the Our Virtual Chapter!
Thank you for visiting our Web page! Part of the PKD Foundation's mission is to provide programs of support and education to patients as we work towards a treatment and a CURE for PKD. We currently have 60+ Chapters that support PKD patients and their friends and families in cities across the country yet, we understand that we cannot meet the needs of all patients with our volunteer led Chapters alone. That is why we are launching the Virtual Chapter! Beginning January 2014, patients from all cities across the United States can join together, virtually, in support of each other. That is really what the Virtual Chapter is all about!
As we work to ensure that all patients have a place to find the education and support they need, we do want to hear from you! Take our brief survey and tell us how the Virtual Chapter can better assist you.
Registration for spring Walks is now open.
If there is not a Walk in your area, the Virtual Walk is for you. Pick a day, time and location that works for you and Walk for PKD. If you are unable to walk, you can use the Virtual Walk to raise money and awareness for PKD.
For more information on the Virtual Walk, email us at firstname.lastname@example.org or check out us out at the Virtual Walk page.
PKD Foundation News and Announcements
May 13, 2015
Chef Michael Psilakis won part 3 of the Chopped All-StarsTournament and will be in the finale with the chance to win $75,000 for his charity of choice, the PKD Foundation. Food Network did an exclusive one-on-one interview with chef Michael after his big win about being on the show and why he's competing for the PKD Foundation.
Read the exclusive Food Network interview with Chef Michael Psilakis
Local Events and Meetings
Virtual Chapter Meeting Webinar
Keeping on Track With a Healthy Diet
Tuesday, April 21
Thank you to all of those that participated in our Chapter meeting! A special thank you to our speaker, Jacob Taylor, MS, RD, LS who presented on staying on track with nutrition.
We would love to hear your feedback on the Chapter meeting and suggestions for future meeting topics!
Meet Our Speaker
Jacob Taylor, MS, RD, LD is a clinical dietitian at Children’s Mercy Hospital and PhD candidate at the University of Kansas Medical Center where he conducts research under the mentorship of emeritus professor, PKD Foundation Founder and renowned PKD researcher Dr. Jared Grantham. He completed his undergraduate degree at the University of Tennessee in 2009 and his graduate degree at the University of Memphis in 2010 specializing in clinical nutrition. After completing his graduate degree, he traveled to Kansas City to complete his doctorate training at the University of Kansas Medical Center. Alongside Dr. Grantham, Jacob has focused his research efforts on controlling dietary factors known to affect ADPKD progression with the development and implementation of the Kansas PKD diet in a clinical study pilot.
Jacob also works clinically as a pediatric nephrology dietitian at Children’s Mercy Hospital where he works with children who have chronic kidney disease, kidney failure, and kidney transplants. He also conducts clinical research at Children’s Mercy Hospital focusing on improving nutrition care provided to children with kidney disease and has interests in conducting research examining the effects of diet and kidney transplant function in donors and recipients. He has presented his research at various conferences including the Annual Dialysis Conference and the Federation of American Societies for Experimental Biology
Visit our library of Virtual Chapter Meetings to view recorded presentations!
If you have questions or suggestions for future topics, please contact us at VirtualChapter@pkdcure.org.
Visit the Virtual Chapter Library to view the archived recording.
View the presentation slides.
Reading Nutrition Labels Handout
Learn More About PKD
Don’t miss out on our series of webinars designed to provide education and information about various medical and lifestyle issues related to polycystic kidney disease.
Click here to visit our learning center and to view our FREE educational webinars!
Unite to fight one of the most common genetic diseases worldwide. Polycystic kidney disease (PKD) affects millions of all ages and currently has no treatment or cure. You can help put a treatment within reach. Join the Run for PKD and raise funds and awareness to support the mission of the PKD Foundation. With your support, we can take steps toward a future without PKD.
Choose to participate in our Half Marathon Series, Marathon Series or participate in a local event while you fundraise for PKD! Learn more.
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Latest Free Webinar
Hear from our new Chief Scientific Officer David Baron, Ph.D., who is also a PKD patient. David shares what we have gained from our PKD research work to date and where we are headed with the Accelerating Treatments to Patients program.
PKD Discussion forums provide a place for patients, family and friends to make connections, ask questions and share stories and experiences.