Some of you may recognize me from the TOS forum. I am finally making my way over here to try and learn about CRPS II as I have recently had that added to my diagnosis. I am still not sure if that is what I have as one of my Dr.'s disagrees. At any rate, I was hoping to get some information from some of you here.

I have been reading some of the threads and find them to be very informative and helpful, but would like to also ask about personal experiences that some of you might be willing to share.

For instance, is anyone seeing a Dr. in the Santa Rosa, San Rafael, San Francisco area that they could recommend??

Also , what kind of med.s are you taking and what types of P.T. are you doing??

I was diagnosed with Tos in 2003 after an injury in 2002, had a decompression surgery in Nov. 2005 and have been doing Peter Edglows home program since. My meds. are Neurontin, Norco, Effexor, diazapam and MS Contin.

I am wondering about adding an anti -inflamatory to my med.s even though there is some tyelno int the Norco, which I take almost daily.

Thanks so much for your help!!
G ~