I went to the appointment to discuss my recent x-rays (to see if the leads moved) and the doctor did not have them. He had a written report which was of no help. In an effort to help me with my never ending pain I am going to have an occipital nerve bolck at the end of September. I was really hoping that my new SCS would eliminate the need for blocks but that has not happened. However, I always get help from the blocks and/or nerve ablation so I am happy to have the procedure. I also started Topomax last night. I hope I do not have the weight loss side effect. If that happens I will have to get off of it. The doctor switched me from Flexeril to Soma at night for the spasms. Both of my SCS's cause major spasms for me! I will go back for SCS reprogramming in early December and see if I can get better coverage for my head pain. I am sure I will be feeling better soon!