by PKD Foundation Staff | Mar 14, 2019 | Transplantation, Voices of PKD
To know me is to know my family and PKD: how PKD defines my family, but does not hold us back. How PKD is in our daily thoughts, but does not hold us back. How PKD challenges us, but does not hold us back. How PKD tests our strengths, but does not hold us back. I am a...
by PKD Foundation Staff | Feb 6, 2019 | Staying Healthy
Here at the PKD Foundation, we love seeing how engaged the greater community is when we reach out for your stories. In the past couple of weeks, we’ve been asking on social media for your best lifestyle tips and wanted to share a few of your best suggestions:...
by admin | Aug 10, 2018 | Voices of PKD
After being placed on the waitlist, receiving the call for a kidney transplant is a happy occasion for many PKD patients. The chance that PKD, with its genetic nature, might not end with a transplant can lead a family down the path all over again. Join guest blogger...
by admin | Jun 29, 2017 | PKD Will Not Beat Me
In a split second our world and our health can change dramatically. We can go from being healthy to severely ill, thinking we are fine while relaxing on the couch and then spiking a fever and dry-heaving while calling 911. This happened to me at the beginning of May,...
by admin | Jun 1, 2017 | PKD Will Not Beat Me
I flew to my birthplace of York, Pa. at the beginning of May to say my goodbyes to my paternal grandmother, who passed on April 11, 2017, and to support my family. I stood in the mausoleum where my grandmother was laid to rest and read her name plate in disbelief –...
