Maggie I did as you suggested and spoke to my GP. He's the only one that has actually shed light on my condition. I guess the medical practitioners thought I got what was happening but I now have a better understanding. The pains in my Ti and T8 were the result of poor bone condition which came from the last bout of cancer that affected my spine when first diagnosed. I know it sounds weird that between 2009 and 2011 evidence of cancer in those areas were disappearing due to my chemo and my supplements (I didnt take any secondary chemo pills or Tamoxifin etc) but I guess the fragility of my spine still remained therefore the collapse of those columns in T1 and T8. My Oncologist increased my Targin, left the Gabapentin as it is and I was given a bone injection at RPH. Dr Ari and I will monitor weight as it's just piling on. He seems to think the Tamoxifin doesnt put on any weight. I'm wondering why he would say that and ignore the obvious. Surely I'm not the only woman concerned about the issue that the landscape of my body, particularly my face is changing. I'm giving one month and if nothing changes I'm coming off Tamoxifin and continuing hardcore on my Isotonix supplements. Don't worry I'm diarising everything. Thanks Maggie. I'm so glad I spoke to my GP. For my spasms he's prescribed my Valiiuim gee what's the other name for it? Ah! Diazapam. Its to help with the muschle spasms. You know a few of the ladies here are on similar treatments I best write the name of their meds and discuss it with my GP.I don't know if I want to go thru my oncologist. i'LL speak to my GP. Well gotta go Maggie. Chat soon I hope. Lots of love, Donna