Team Teddy Bear is the team our family has formed for the annual Walk for PKD. I initially created this blog as a way to track our fundraising progress, but have since expanded it to share our experience with Polycystic Kidney Disease and just about anything else going on in our lives. First time visitors may wish to read Our PKD Story which relates our personal experience with PKD. Please do feel free to leave a comment on anything - even just a quick hello letting us know you stopped by.
Saturday, August 16, 2008
more press for our cause
Laurie Hlavarty, the Healthy Living/Families editor at the Poughkeepsie Journal contacted me via email yesterday evening stating that she plans to run some sort of article relating to PKD and our walk sometime in September. That's all I know at the moment, but I'm very excited. Earlier this week, the paper ran an article about a man from Red Hook who participated in a four-way kidney swap down at New York-Presbyterian Hospital.
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