Hi, I have been a member of an LC support group on AOL for years. Everything there has changed so much, except the wonderful people. I have just had my annual Ct Scan and going through the wonderful W___time to find out what is going on. My main purpose now is to let the newbees know that there is hope and to stay positive...I'm talking big right now, cause I don't get my results until the 20th. I lost my best friend to lc after 26 months. She was dx'd after me. Her sister now has adenocarcinoma in both lungs. We all live on the same culdesac. I now have Ct scans once a year.it is always scary, cause there is so much pain in the surgical area. Here to share, give hope. Jan