Hi everyone!

I finally was seen at John's Hopkins Univeristy yesterday. YAY! They want to install a SCS next month and also want me to be a "trial" patient for them!

Want me to be their example of what does and does not work for RSD. I was very happy to know that all of my doctors are experts on our condition. I was taken very care of and treated with utmost respect. It was tremendous! I now have a new respect for doctors who actually research different conditions and seek the best treatment for their patients. Just incredible!

I am still a bit leery on the legality of it all. They will compensate me. Which I don't worry about (I would rather do it to help someone), I know it will be public. (No problem). No meds will be given. Still; there is a nagging doubt. I think fmichael would really help me with this!

Hope all goes well!

Kim