Guest guest Posted April 16, 2001 Report Share Posted April 16, 2001 I am participating in a fund-raiser for the CFF which is called Tea Time. It is similar to the Mother's Day tea that others have mentioned. What I like about it is that I have all the donations go right back to the CF Foundation office in Atlanta. That way, the people I send packets to know that I'll never know whether or not they donate. Since I am one of those people who hate to ask for money, this was easier for me. I still hate it and am not sending out many packets, but it's something. I don't know much about the CF Foundation other than what I have read on this list. The literature with the fund-raising materials claim that over 95% of the Tea Time proceeds go to research. I realize many of you have a bad experience with the CFF, but if it wasn't for material that they sent me, Mycah might not have been diagnosed as early as she was. I had to convince her doctor that's what she had, and it was their info that gave me that ability. Anyway, that's my story and I'm sticking to it. Lori in Florida Quote Link to comment Share on other sites More sharing options...
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