Up for a PKD Challenge?

“By a show of hands, how many people know what PKD (polycystic kidney disease) is?” This is how I begin most of my speeches. I have asked that question at over 80 events. I continue to be amazed as I scan the room and so few hands are raised. This shows me how vital...

The Bloody Truth

It was several years after my transplant as I sat in a lecture at Johns Hopkins University School of Medicine with a room full of med students. I looked up at the overhead projector and saw the MRI of my kidneys before they were removed. My nephrologist, Dr. Watnick,...

Have Meds, Will Travel

Organization helps me stay positive. Especially when it comes to organizing all my medicine. I don’t prepare for a trip like a normal person, say someone with two kidneys.  This past weekend I had an assembly line party of pill packing and the party consisted of my...

Knowledge

Knowledge, the “K” in my PKD! Rather than fear, try and understand! This is what I live by. When first learning of PKD, or after living with it for almost 20 years, like myself, it can seem scary. I have learned that the more knowledge I have gained, the more...

A+ for the Affordable Care Act

At the end of every PKD Educational Seminar I have attended, there was always one question that broke my heart. A mother or father would raise a hand and say: “I am afraid, for health insurance reasons, to get my child tested to determine if they have PKD.” I would...