News and Information
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
Chapter Educational Meetings
The PKD Foundation Memphis Chapter hosts monthly PKD information and educational meetings in conjunction with Jyothi Pinnaka, MBBS, MD, FHN, FASN and Transplant Nephrologist, Clinical Assistant Professor University of TN Health Science Center, Memphis.
Meetings are held the 4th Tuesday of each month at 2:30 p.m. at Dr. Pinnaka's office located at 6005 Park Ave, Suite 825B, Memphis, TN.
Tuesday, September 23
2:30 - 3:30 p.m.
Dr. Joythi Pinnaka
6005 Park Ave.Suite 825B
Memphis, TN 38119
To RSVP or for more information please contact Karyn Waxman 901.491.4799 or email email@example.com.
Virtual Walk for PKD
Walk your way in your local community
For more information, click here!
May 19, 2014
Presented by Howard R. Winokuer, Ph.D.
Dealing with the reality of PKD is a very difficult situation. It is challenging to know how to talk to your children, even young adults, about PKD. As a result of attending this webinar, you will understand how to talk with your teen or young adult about PKD. Our presenter for this webinar is Howard R. Winokuer, Ph.D. Fran Towey, Jr., and his daughter Katie will also join us to share their story of being diagnosed with PKD as a teen.
PKD Discussion forums provide a place for patients, family and friends to make connections, ask questions and share stories and experiences.