Went to my neuro regarding the brain lesions. He was a very nice man and listened to everything. Took detailed notes. I told him all my symptoms and he reviewed my films. He came back in with this confused look on his face. He said that he has not seen this very often but was just talking about this with another doctor that day. He said my lesions "could" be early MS but probably not. I need to have another MRI in six months. We started talking about CFS and he said that he was talking to the head of Neuro and another doctor today and there was an article regarding "non-specific" brain lesions in CFS patients. The head of the department is doing some research on it because they are starting to see more and more of these lesions in people who also have or will have a diagnosis of CFS and FM. He said he is going to do some research but suggested my next stop be a Rhumetologist because my symptoms are defenetely not caused by the lesions, but the lesions are a symptom of the problem. I feel like this was good info that maybe Neuros are looking into this too.