Anyone been diagnosed with myofascia pain syndrome (MPS)? I suspect that a great deal of my pain is from MPS. Check out this website for one of the best descriptions of these problems:www.sover.net/~devstar/Devin Strlanyl is also the co-author of "FMS and Chronic Myofascia Pain Syndrome," the most comprehensive book I have ever read on the subject. I was shocked when I first read the info on this website. It described my pain exactly and treatments that my doctor has never mentioned. He tells me I have a chronic pain disorder and have to learn to live with it. I am looking for a new doctor...one that will be more open to discussing treatments and at least giving me some answers for things I come up with in research. I live in pain 24/7 and am always looking for answers.I did find through this website several recommended doctors in my area. One is chief of rheumatology at a local hospital and when I searched on his name I found a number of articles and papers he has written on FMS and MPS. I called and left a message today for an appointment. It seems to take a long time in the Dallas/Fort Worth area to get theumatologist appointments, but I will wait as long as it takes to get in with a doctor that knows what he is doing!Paige