Seth - Living with Primary Hyperoxaluria Type 1 (PH1)

This video is created for US audiences.

In this video Seth, as a combined liver/kidney transplant recipient, discusses his experience with kidney failure and being diagnosed with primary hyperoxaluria type 1 (PH1). PH1 is a rare inherited disease in which a defect in the liver causes overproduction of oxalate - a toxic metabolite - leading to irreversible damage to kidneys and other organs.

Seth and his caregiver and girlfriend, Sarah, discuss the importance of healthcare professionals considering genetic testing to enable accurate and timely diagnosis and visiting their doctor to stay on top of their health. Learn more by visiting: www.TakeOnPH1.com.

PH1-USA-00121