It's been a while since I've posted something so I thought I say hello to all you fellow FIBROMITES. HI! Been taking the cymbalta and it has helped me to some degree, (6 weeks now). Besides the constant sweating that comes with taking this med I have noticed a slight increase in of energy. Still the pain and muscle spasms continue to hurt and burn like heck! Im wondering if I request my doc to up the dosage, if it would help. Any advice wouold be appreciated! Night. Tanya PS. back in school again, one day out of the week I'm volunteering at the habitat of humanity and I begin a PT job at Hogares Inc., as a BM working with children and adolescents. I hope I have not biten off more than I can choose. Thinking & planning for my little man's future. Have to try and beat this thing one last time!!! Wish me luck!!!!