Well, I have received the reports I asked for - the letters to my GP, the ct reports and the ct images themselves. In one way it's made me angrier than before because five of the affected sites are clearly listed in one report but the oncologist claimed he didn't know where they were.
In another way, it's put my mind at ease, seeing for myself the extent of the mets. It took quite some doing, staring at images of normal liver CT scans on google and then comparing them to mine, but I did it and can see for myself that the three mets there have more than halved, which I'm chuffed to bits about.
I haven't yet investigated normal bone images VS my bone images - this is a job for this weekend.
The reports also mention a couple of other things - non-cancer related - that they couldn't be bothered to tell me about but which explains quite a few recent niggling little things so my mind is at ease knowing these symptoms are not related to cancer.
