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The site melissa talked about is at MSN it is under the search head of Cystic Fibrosis 2 Chat. I love the site they allow people to be their selves and don't bitch and whine either.Angie living with CF not letting CF Live with me
Thanxs I found the group waiting for me to be accepted the post are great there really nice people who listen and not judge you.Kathy 18 w/CF Diabetes MRSA
Wow I haven't posted in a while and now my website is the talk of the boards. Thanks guys. What happened to make people want to go there. If this Angie is on this website I haven't had her be a problem. I;m the manger and if there is a problem it is dealt with privatly to whre no one can butt in and cause more problems. We do get into some good debates but nothing bad. Just saying. Thanks guys for spreading the word for my group's site.Amanda
Angie,Hi my name is kelli and im 23 with cf. Could you email me that cfchat address.Here's my email address DitsyBlondChick1@aol.comI am really interested in that cf chat .Thanks,Kelli
CysticFibrosis2chat@groups.msn.comJust copy and paste. A very nice web site great chats and discussions not judgingAngie 43 living life to the fullest w CF
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