Hi cattys,
I'm so glad you asked. Never worry about asking me any questions. How's your leg, by the way. I know you were supposed to go to the doc Monday.
I've had the pump for almost two and a half years and I still LOVE it. It works really well for me. They usually increase it every time I go to have it refilled which is now, every two months. It got to where I was going for refills every month because they kept increasing it so the pump would empty faster. (I hope this makes sense) So, she ordered a higher concentration (double what it had been) and for now, I won't have to go back for two months. As the increases occur, that time in between will diminish and I guess she'll order a higher concentration again.
It's been absolutely the BEST thing I have ever done for the RSD. I have morphine and bupivicaine in it. The bupivicaine is almost like having a constant block in a way. It's not as strong, but it's still kind of like a block. I've noticed that since the pump, my legs aren't as purple and don't turn as hot as they did. I never thought that the pump would help that. I also noticed that I'm not sweating as much. I'm sure all of this has to do with the bupivicaine.
Are your docs talking about a pump for you? Before I had mine put in, he did a trial. My trial was one injection (I guess of morphine) right into the spinal area and then I had to chart my pain levels for the next day. I stayed in the hospital for about fifteen hours and went home that night. I've heard of other trials where people have a temp pump that they go home with. It's a longer trial. Kind of like the stim trial I had. Maybe you had the same type of trial for your stim. Any other questions, please let me know. I'd be happy to answer any that I can. Hope your leg is feeling better.
Sharon