I have a friend in Idaho who's daughter has Cystic Fibrosis (CF). A year ago she crashed and had to have a double lung transplant. She has written a blog that chronicles her ordeals, her faith, her highs, and her lows.. That she is alive today is a miracle. I thought it good enough to post a link to her blog on our sideboard to the right. I think that for it to make more sense you should start at the older posts and follow them to the present. Her name is Jamie. If you know anyone who has Cystic Fibrosis, refer them to her site, it would be worth their time. She is more than willing to communicate with others about her illness, and has done so with many people.