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.
Sunday, September 12, 2010
PKD Jewelry Fundraiser
Check out Ruth's Lemonade and Kidney's blog to see some nice pendant necklaces which are available to purchase. More than half of the proceeds from the sale of the necklaces will be donated to the PKD Foundation.
Bob, thank you so much for sharing the links!! Sending warm thoughts.
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