Came across this today and thought it had some good ideas.
The Give List
On April 23, 2003, Colin was born with cystic fibrosis. After undergoing surgery for a ruptured bowel at two days old and spending a month in the hospital, we attended our first CFF walk only two weeks later. We've never stopped fundraising since then. This (occasionally posted to) blog highlights some of the things we do to raise money and some of the news on the progress of cf research.
Catching Up after a successful Wine Event
It's been a while since I posted anything. The wine event had us really busy and then it was right into the holidays. The wine event was a fantastic evening. Attendance wasn't what we had planned, but in hind-sight, this is a good thing. We had a packed room. The sommelier, Arthur Black, went out of his way to travel up from Indianapolis to be present for the event and give it some prestige. We had the opportunity to go out to dinner with him the night before and it was interesting and entertaining. I'm not a big wine lover myself, but the way he described the wines we tasted and the things he pointed out showed me a whole new side of wine. Back to the event, the turnout was great and the attendees were generous, which was a lt to ask given recent economic events. There were a couple of surprises in the Bid for a Cure following an amazing speech by Rosie Woods. Rosie is 45+ and has cf. Back when she was a child, she was the poster child for CFF one year. Like all parents at that time, hers were told she wouldn't see ten years old. At her age, it's a fantastic case for never giving up hope. Check out some pictures from that night.
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more about "2008 Uncork A Cure Wine Event", posted with vodpod
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