I just handed him a long list of symptoms and said I think I have CFS. He ordered a series of blood tests to rule out other things. They took 5 vials of blood. I told him I had been diagnosed with FM by one rhuemy and then after that another dx me with familial mediterranean fever but said he thought I did not have FM. This doc today was a PCP. He said that no one in his practice has been dx with CFS. Is this something that is hard to get diagnosed? Do docs not want to see this, I got the feeling like it was a rare thing. He said after the blood work then we would go from there. He metioned seeing a infectious disease doc and a "fuzzologist" (spelling?) which he explained that was a muscle doc. He did up my zoloft, but did not give me anything for pain or sleeplessness. I am feeling a bit better today than I have been, but still wish he had of at least gave me something for the aches and pains until we can know something. I felt he is a good doc, but I did not get to explain myself or really tell what has been going on. I guess I will probably get that opportunity in the near future.