I've been rooting around the Fibro 101 thread and reread the link on Myofascial Pain Syndrome. I'm quite sure I have this too because when I get a massage, I'm lumpy and Victoria has to gently work on those spots to try to smooth out the muscle. The massages really help me.
Anyway, there is a 2009 update of symptoms on that link and it sure sounds like a lot of us! The person who wrote this site is a researcher for fibromyalgia and chronic myofacial pain syndrome. She is not a doctor. She feels that fibro and MPS are two separate illnesses. I've seen other sites that say they are beginning to believe these are connected. Actually, I really don't care. Just find a way to fix it! 
But, the information here sounds like us so I wanted to share it with you.
http://www.sover.net/~devstar/phsympt.htm
Sherrine