What do we do? If I took this to my doctor she'd probably admit me in a loony hospital..she would say I dont know nothing about that or she would say we dont test for that around here. Then where does that leave us. Right where we started from. Yes I'm sure we could send our blood away and have it tested or maybe fly to California to see the doc but who can afford that..I sure cant. I think its great that they are finding all this out and maybe in 30 yrs or so my grandchildren will be protected but I just get frustrated when I want someone to help us now. I'm not putting anyone down on the board for posting these things but wouldnt it be nice if our healthcare system could figure it out and make us all so were not in pain, etc.... I admit I get alittle overwhelmed with all this(blame it on the fibro fog)I just wish someone could find a cure.