Thank you for the welcome to this forum. My husband has struggled with this disease for nearly a decade and what might be worse than the pain, is the view that people have with this disease, just like they do with Chronic Fatigue. They don't see a scar or a physical reason and they don't believe you are really in pain. They just think you are being lazy or imagining it. We have this trouble with my husband's family especially. What they don't see is a man who lies in bed at night, hurting in every part of his body, and nothing brings relief. It is a kind of pain that is raw and constant. I'm also glad that some medications are being researched for use for Fibr. patients. I will be reading all of your threads to see if I can discover something new (or old) that might help him. Thank you again.