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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."
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common, life-threatening genetic diseases, effecting 600,000 Americans and 12.5 million people, worldwide. ADPKD affects more people than Down syndrome, cystic fibrosis, muscular dystrophy and sickle cell anemia combined. PKD affects men, women and children of all races and ethnic origins.
Common symptoms of ADPKD include high blood pressure, pain in the back, side or stomach, blood in the urine, kidney stones, frequent urinary tract infections, a family history of kidney problems, heart problems or strokes
Autosomal recessive polycystic kidney disease, ARPKD, is a rare genetic disorder, occurring in approximately 1 in 20,000 individuals. It affects boys and girls equally and often causes significant mortality in the first month of life.
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