I was so fed up with telling doctors I thought I have it in both hands and then getting nothing for a response, that I email begged my PCP for hand xrays on Thursday, had the xrays on Friday and the radiologist’s report on Saturday, and yes I am not crazy, I have it in both hands. I feel vindicated, but not victorious. Why? Because I also know I have it in my gut, my eyes and my eyebrows. There is no scientific way to prove these complaints are CRPS related, but damn they make my life miserable. I was just lucky that I had a fall in 2015, because there were hand xrays to compare. No CRPS, back then nothing.

I truly believe if I had never taken LDN I would be in a nursing home waiting to die.
My reason for writing this post is to tell you, don’t give up. And if you think it is CRPS, it probably is.