Team Teddy Bear

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.

Monday, June 18, 2012

Rockland Boulders PKD fundraising event

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  The Hudson Valley Chapter of the PKD Foundation presents a night with the Rockland Boulders!   Join us on the evening of ...
2 comments:
Saturday, September 17, 2011

one week until the 2011 walk

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The 2011 Walk for PKD is only one week away. Thanks to your generosity, our team has already raised more than $2500 to help in the fight...
2 comments:
Sunday, July 24, 2011

2011 Walk Letter

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The Hudson Valley Walk for PKD is coming up two months from today. Following is the letter that I sent out to friends and family about a we...
1 comment:
Monday, July 18, 2011

another link in the chain

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A few months back, I posted about Barbara, who is Jeanne's kidney donor, and Karen, who is Barbara's daughter. I am grateful that ...
Saturday, June 25, 2011

four months later

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Today marks four months from the day of my surgery - and about 10 weeks since my last blog post. I'm happy to report that everything ...
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Monday, April 4, 2011

followup #3

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I had another followup visit with Dr. Del Pizzo today. He's happy with how the wound is healing. I will need to continue to pack the w...
Saturday, April 2, 2011

A week without a doctor's visit

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Yes, it is true. My family managed to make it a whole week without a single one of us visiting a doctor! No clinic visits, no surgeons, no...
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Bob
Verbank, New York, United States
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