Thanks so much for all of your kind words and advice. The pins and needles went away so I dont think they had anything to do with the RSD- Since most pains usually stay I can see how we all can jump to RSD conclusions so fast. I have not had that rebound feeling with the Roboxin so that was good too.

I went to a new neuro and she didnt believe I have RSD b/c she couldnt see anything = I was sooo frustrated with her I just couldnt take it. When I told her my RSD spread after my hip replacement she kind of rolled her eyes like it doesnt spread like that!! I could go on but I am not going to relive it. I am staying with my old neuro...

I am really trying hard to create new pathways in my brain- using visual imagery and extreme distractions to my pain. There is a whole science to this- Retraining the brain kind of thing- I also bought a natual seratonin that I am going to try because I cant tolerate the SSRIs

So thats my story for today- could change tomorrow-lol

Deb