I was diagonosed with Mel in 2008, stage 1c, I had a WLE and no further treatment necessary. I do visit my derm every 3 months and they have found several basil cell carcimoma's which we treated and seem to be ok. I started to feel very fatigued a couple of months ago and went to the doctor in which she did blood work and everything came back fine. She then sent me for a MRI in which they found a mass on the liver which they cannot identify and are watching until march when I am supposed to have another scan. when they scanned my liver they saw a 4mm spot on my right lower lobe of the lung, sent me to a pulmonary doc and he did a baseline scan again and they found another 2mm spot on my left lung and a mass on my thymus gland. I never even heard of a thymus so I asked him about it and he said not to worry that we will just watch it and in 6 months rescan. I left there feeling very confused so I came home and researched this and from what I gather is scarey. I think I want a second opinion and not sure of what to do at this point. I have a spot on the right and a spot on the left lung and now a mass on the thymus gland, my nerves are shot and I hate the waiting game.