|
|
SALT LAKE CITY CHAPTER - Providing Hope and Support
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 raise find a treatment and cure for PKD.
Chapter Coordinator: Karen Ungerman and Amy Folker
SaltLakeCityChapter@pkdcure.org
If you would like to contact the Salt Lake City Chapter by phone, please call 1-800-PKD-CURE.
|
Connect with other PKD patients and families in your area.
Currently we do not have any meetings scheduled. Check back often for updates or contact Karen Ungerman at SaltLakeCityChapter@pkdcure.org for more information.
Join in a variety of fun events.
|
|
National Convention on PKD - Summer 2009
The National Convention on PKD is the only opportunity, worldwide, for PKD patients, their families and and medical professionals to learn about PKD and connect with others in the PKD community.
In 2009, the convention will be held in two locations:
Chicago, IL and San Diego, CA
Visit www.pkdcure.org for more information!
|
Learn More about PKD.
Webinar on PKD: "Basics of PKD"
Tuesday, October 14th, 2008 at 8:00pm (ET)
The PKD Foundation will host its first webinar Tuesday, October 14 at 8pm (ET). This free webinar “Basics of PKD” is open to everyone. The presentation will be conducted by Dr. Ron Perrone, Associate Chief, Division of Nephrology of Tufts Medical Center (Boston) and Chair of the PKD Foundation Scientific Advisory Committee. A question and answer period is also included. This will be the first in a series of quarterly webinars designed to provide education and information about various medical and lifestyle issues related to polycystic kidney disease.
For more information on this Free Educational Event and to Register please click HERE.
Make a difference in the lives of 12.5 million people.
There are jobs for everyone, big and small. Just contact us at SaltLakeCityChapter@pkdcure.org to find out how you can make a difference in the lives of 12.5 million people!