Re: CMP question
Yes, the CMP in my screen name is because I have chronic myofascial pain and have had it for several years. I also have other medical issues that contribute to my chronic pain, but my CMP is pretty severe and widespread, and is what tends to be the most debilitating for me.
I would be glad to answer any questions you might have and if you get a chance to take a look at my story in the other sub-board, please do. It gives some brief info on CMP and what it is about. I can tell you right off the bat, that it is a very misunderstood disease and there are many in the medical community who do not acknowledge it as a real diagnosis. But I am living proof that it really is and that it can be very painful.
Welcome aboard, and as I said, please feel free to ask anything you would like. I don't have all the answers, but I will do my best. Take care, CMP/MM