Hello. So nice to meet you all. I suppose, like everyone here, you get a sense that inspite of being alone mainstream, you are not the only one that feels this way. Two months ago the Chief of Infectious Disease, who had diagnosed me three years ago with CFS, informed me there was "nothing they could do for me". Sick and tired of being sick and tired (smile). I tried to contact two local support groups but it never came to fruition. My first thought was "everyone is too tired". I am delighted to learn of you and look forward to helping make a difference. Thanks for renewed hope.