Hi all. I apoligise for taking soo long to thank you for the support and helpful links, I really do appriciate the effort everyone puts into this site. This is the forth time I have written this and I type with 1 finger ( they should make bigger keyboards for people with acromegaly. I think I use the backspace button more than any other).lol.. Honestly my computor kept crashing. I had to reformat the harddrive and start from scratch. If only it were that easy to fix us. lol.. Yes I did have surgery ,about 8 years ago. After the post op tests the Endo said the surgery was a waste of time and that I would have to have radiation and injections every 8 hours, and I would also need to have my gall bladder out. I asked lots of questions and got no answers. He told me that he knew what he was doing so I didn't need to. He said if I didn,t do as he said that I would be dead in 5 years and crippled before that. I walked out and haven't been back. I come here every now and then, when I am feeling sorry for myself. It reminds me that I am not the only one with this f..........g thing. I also check to see if anyone has come up with a miracle cure or something. That is why I was asking about Pegvisomant . It sounded good in the article I read. Thanks again Ian... | 