August 19, 2014
As part of the PKD Foundation's Accelerating Treatments to Patients program, we fund PKD-related scientific meetings that bring experts together and provide continuing education for health professionals.
We were a major sponsor of the Federation of American Societies for Experimental Biology (FASEB) Science Research Conference on Polycystic Kidney Disease: From Molecular Mechanism to Therapy Aug. 3-8, 2014, in Italy. The international conference welcomed prominent scientists working in areas experiencing rapid scientific advances and conducting cutting-edge research.
July 16, 2014
Kriste Lewis, a 40-year old mom with polycystic kidney disease (PKD), has become a New Orleans Saints cheerleader.
Lewis, who is a dance instructor, decided to fulfill her lifelong dream when she turned 40 and tried out for the squad last April. She said she used her age and health issue as an inspiration.
"Fourteen years ago I was diagnosed with polysistic kidney disease," Lewis said. "Eventually my kidneys will shut down [and] I will be in need of dialysis and in need of a transplant."
"That had a lot to do with me auditioning as well," she said. "I didn't want to waste a day."
Read more about Kriste and watch her interview on ABC's "Good Morning America."
Voices of PKD
The Transplant Games of America are special to sisters JoAnn Villanueva and Suzanne Ruff, and their entire family. JoAnn has PKD, and Suzanne does not. In 2004, Suzanne donated her kidney to JoAnn. "The Games started as a way to show the world that transplants work," Suzanne said. "It is a celebration of life as donors and recipients come together."
Their first experience with the Games came in 1994 when their mother, Joan Gill, participated and won the bronze medal in golf in her age group. Joan received a transplant in 1988 after ten years on dialysis from PKD.