The whole thing about people who make full recoveries and people who only make partial recoveries from this horrible illness is still very vague. For example, when I read things on the internet the consensus seems to be that full recovery is unlikely but having known a couple of people who have had the illness. They have recovered completely after a couple of years. The question here is are there various forms of the illness and have these people had true CFS? Its almost like the diagnosis of Irritable Bowel Syndrome. If the doctors don't know the problem they put you in this hole. I have been given a diagnosis of Post Viral Fatigue Syndrome after I had a Hep A injection and a period of stress. This has lasted 10 months so far and progress is slow. The symptoms have included nausea, bloating, tingling, headaches, brain fog and lack of concentration but so far no fatigue as such. These symptoms have been debilitating in there own right. The other thing I have found is high levels of Copper from a hair sample. Do other people have this particular problem? I would love to think that this is the cause of all my problems but I think that is unlikely. Are there people on here who can say they have made full recoveries?