Hi everyone, I am just here to introduce myself I guess. My name is bryan, I have been told I have crps for months now by a few doctors and a physical therapist. Just today though I have been "officially" diagnosed by a wcb doctor. I've read up on it... and it seems my crps is different than alot of people. My foot is like burning cold... not hot. Feels like my foot has permanent frost bite It sucks. I live in central Alberta, and I'm definitely not looking forward to the long winter again. Cold aggravates my foot making it feel impossibly colder than it already does. All I know is that I am going to have to deal with this one day at a time, and keep trying new treatments until I find one that hopefully will work for me.