Guest guest Posted March 26, 2003 Report Share Posted March 26, 2003 Toni's chat has ended. The other CF chat is up and running and very popular . The details are below.We have patients of all ages attending, parents of CF folks and lots are great support and information - and fun things too. We had a lung trivia night last night which is always a lot of fun. ~~~~CF CHAT~~~CF CHAT~~~EVERY DAY NOW~~~CF CHAT~~~CF CHAT Cystic Fibosis 2 Chat Welcome to patients, siblings, parents, support persons. Discuss all that concerns you. New medicines, new therapies, doctors, CF centers, lung involvement, weight issues, lung transplant, working, parenting etc. Now we can chat everyday!!! Here are the MSN CF2 CHAT TIMES: EVERYDAY: 2 PM Central, 3PM Eastern EVERYDAY: 8 PM Central, 9 PM Eastern How to get there: MSN Groups> Health & Wellness> Support Groups> Heart & Lungs> Cystic Fibrosis 2 Chat or http://groups.msn.com/CysticFibrosis2chat/homepage Hosted by Berrie, 20ywcf Joanne M. Schum Cystic Fibrosis Bi-lateral Lung Recipient September 12, 1997 University of North Carolina Hospitals Chapel Hill Residence: Upstate New York email: luckylungsforjo@... " Taking Flight - Inspirational Stories of Lung Transplantation " Compiled by Joanne Schum Authored by lung recipients around the world http://www.trafford.com/robots/02-0497.html http://www.trafford.com/ Joanne Schum twoluckylungs@... Bi- lateral Lung Tx 9/12/97 Quote Link to comment Share on other sites More sharing options...
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