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Polycystic Kidney Disease (PKD) affects 600,000 Americans and 12.5 million children and adults, worldwide. There is no treatment or cure, but there is hope.

The PKD Foundation is the only organization, worldwide, dedicated to promoting research to find a cure for polycystic kidney disease (PKD) and improving the care and treatment of those it affects. Our vision is that “no one suffers the full effects of PKD.”

The reason PKD was chosen this year is because I (Paula Sue Swope) have personally experienced this genetic disease. My maternal grandfather passed away from PKD. So have my Mother (on peritoneal dialysis for 18 years) and her sister (received a donor kidney). My uncle is still alive with the help of a donor kidney.

Nov 3, 1998, I gave a kidney to my sister. Today, my kidney is helping her lead a normal life. She will always take anti-rejection medication and she suffers from complications from the diseased kidneys she still has and from the medications she takes. She has two children; a daughter 18 and a son 16. I pray they don’t have the disease but, if they do, I hope the PKD foundation has found a cure or a treatment.

Thank you for helping the Gaited Gala donate to this foundation.

Paula Sue Swope

Me with my two sisters; Vicki and Karen.
Visit the PKD web site!

http://www.pkdcure.org/

 

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