Posted 2/26/2009 11:41 PM (GMT -7)
Have any of you seen a pain specialist? My GP is referring me to one. I have mixed emotions about this for one reason or another but am open-minded. I've been on vicodin for the last 3-4 months but it's effectiveness is rather insignificant (of late). I want to be more functional and get to the point where I can enjoy some aspects of my life? My concern is that the meds may make me feel better (less pain) but hinder my ability to function well at my job. I would love to hear experiences of Lymies that have used a pain specialist or center. What types of treatments were used? What were the results.
Thanks for you input.