Hi dr smith, we have tried, I used to live in the UK for 15 years and took dyhdracodeine or df118 as it's also known. I took 20mg a day and for 15 years had no problems whatsoever, now bowel blockages, no personality issues etc. Then I had the head on car accident that changed my life (not my fault) and came home to Australia. Aus don't do df118. They stopped it in 2002 and we moved back in 2005. So we began a trial of what works etc, the long and the short of a number of drugs, so many I can't recall but here's a few, tramadol makes me vomit violently, durogesic patches I'm allergic to the adhesive, and a number of non opioids that didn't do anything. I used to have rhyzotomies every 6 months from 2006 but they stopped once I had the seizure. So now I have the stim implant and I just use the slow release oxy, which, doesn't give me the short temper, it's the endone and oxy norm fast acting for break through pain that do. We have also tried endep 25mg and 10mg but I have bad side effects that result in tremors and since the seizure, also a no go. tried Valium which made me feel sleepy and given I was working at the time I needed my brain switched on so had to stop, then they put me on Xanax but I heard such horror stories I stopped and went through 4 days of withdrawals and given I was only taking .5mg I'm never putting myself through that again. The sad thing is they really helped considerably. So, I'm really hoping they can get this stim sorted and I can get my life back med free. Yay, I'm seeing the rep and PM on Wednesday 22 and believe they will discuss the paddle implant. Any things you can suggest?