Thanks to all of you for previous encouragement to see a rheumy who treats FM. I finally received the diagnosis I've been searching for these past 7 years -- fibromyalgia and Mayofacial Pain (sp?). I'm not surprised I have FM (I knew it years ago), but I am surprised to find a doctor whose diagnosis wasn't "everything is normal," "there's nothing medically wrong with you," "I don't know," or my personal favorite, "lose weight and exercise." YIPPEEEEEEEE! She's putting me on meds to help me sleep and continuing with the Vioxx and wants me to do water aerobics and take some supplements. Anything else I can do from you veterens? What is MP? Thanks again. I encourage anyone still undiagnosed to keep trying -- it's such a relief and a personal validation to have an official NAME attached to why you can't do things, etc.