Living in pain with a 3kg kidney
“we wanted to share a story from one of our community members that addresses the issue of pain and demonstrates the complexities of the disease.
“we wanted to share a story from one of our community members that addresses the issue of pain and demonstrates the complexities of the disease.

By Helen A dozen years ago, Judi and I were two mums who shared a school run for our boys. Our biggest worry then, was

By Graham Bradley I discovered that I had PKD back in 1989 after a four-wheel driving adventure on Fraser Island. The rough terrain managed to
By Charmaine When my son was born, there were already tiny cysts growing in his newborn kidneys. I knew there would be a 50 percent
Guest Post- Janice Creenaune My name is Janice Creenaune and I have PKD. My mother has PKD. Her sisters had PKD and my daughter has
Guest Post – Vanessa Cullen Like many people with Polycystic Kidney Disease, I was not aware of having this affliction until my thirties and were
Guest Post By Alicia Faehrmann An old friend once asked me if I could have a superpower what would it be? And I replied with
Guest Post – Alicia When I was diagnosed with PKD almost 3 years ago at age 22, I took it as a death sentence. But

Guest Post by Jenni Miller I first heard of PKD in early 2003 when I met my father-in-law, Peter. He was on a dialysis machine

– Written by Vanessa Cullen With a life history of several serious health conditions I have always been forced to engage with my own health.