Well, yesterday I had my 7th esophageal dilation since August 07. I also have to have another one in a month. I finished my radiation in June 07. The radiation caused my upper esophagus to shrink causing a severe stricture. My GI doc said that he is hoping my esophagus will eventually stay in place, but he said it could go the other way too. I am very concerned that if it goes the other way I will never be able to eat again at all. It could also mean that I will be on a peg tube for the rest of my life. It really scares me to think of that happening! I am still on the peg tube but never use it except during the few days after the dilations because my throat and esophagus are so sore I can barely swallow. I am hoping that the outcome of my dilations will be a positive one. Just looking for emotional support, encouragement and for stories from others that have had these problems with their esophagus. Thanks!