I am new to this forum (first post) and for that matter, relatively new to the world of this wide-spread muscular pain and debilitating fatigue. In the last four years or so, I've been seen by so many doctors and tested for so many different things. I may even have in my medical record a misdiagnosed clinically determined dx of Myasthenia Gravis. Granted, the fatigue part has only become a major part of the picture in the last 18 months. Before that, my biggest complaint was extreme muscle tightness. And I wonder now, if what I would have always desribed as tightness, others would desribe as pain. And the moments that I am feeling normal just seem to complicate things as I, even now, ask myself is this for real? Anyhow, just wanted to expess my joy in finding this thread and the wealth of associated informative content. Even if I discover that my health issues are not exactly related to ME/CFS, I am sure to find some worthwhile information here. Thanks to the information I found on this page, http://phoenixrising.me/treating-cf...nding-a-chronic-fatigue-syndrome-mecfs-doctor I discovered that I live only about eight miles from a Fibromyalgia & Fatigue Center. I can't remember the last time I actually looked forward to the next day as I will certainly be calling them tomorrow. Lastly, I do realize there are those who go years and years feeling like their life is in a downward spiral with no end in sight with an illness like this, and I promise to pray for you.