Thanks Jewells

Your info is always great! I am so pleased for Jeffrey - and hope to giving a similar story after the surgery !!

I think there are 2 different stimulators? I'm not sure - but I think the research I did showed me there were a couple? but I could be wrong. I reckon the consultant probaly is going worse case scenario becuase he knows I can't travel well, so that will always be a large factor in anything I decide on (it's about an 8 hour round trip to see him which then usually puts me in bed for a couple of days after because of the pain).

I had a look at the website - looks great! I have checked some of it out before but not in as much depth. My dr said the same thing about the brain, and given that she's just told me she doesn't feel there is anything she can do for me she told me to just go for it - it would be pretty hard for my RSD to get worse!!

Thanks so much for all your help! I know this should be an easy decision, it's just I find it hard!!

Love to you and Jeffrey!!

Rosie xxxxxxxxxxxxxxxx