Can anyone describe how bone mets feel like? Was the first pain you felt very strong? I am scared. Last summer they suspected mets in my pelvis bone and in one of the lower vertebras and in my shoulder blade. They wanted to take a biopsy in my pelvis bone, but I refused, because I felt no symptoms, and they said that if I had bone mets they wouldn't be able to do anything about it. The last few months I felt pain in my lower back. Not strong pain. It feels sore. Yesterday, when I got up from a chair I felt a sudden strong pain a little above my lower back, near the spine. It is still there. It is endurable, but it does bother me. It doesn't get better when I lie down. I will wait and see for a couple of weeks. If it doesn't get better or if it gets worse I might let them take a biopsy. But I don't know. What's the point when they can't do anything about it? You who have bone mets, do you get any treatment? What treatment? And does it do you any good? And what about side effects? My primary tumor was in my left submandibular salivary gland. That was 16 years ago. I had surgery and radiation treatment. vintage evening formal wears sales back to 1920s