PF,

I hope you get LDN ASAP. I believe it saved me. I sound like the LDN nag, but I cannot help it, because I know it works, is non-invasive, cheap and has no down side compared to other treatments.

The only semi-pain relief I had was hydrocodone, but I did not want to take it because of the Tylenol, plus I was not allowed to take it at work when I needed it the most. No doctors would give me anything else other than neurotin, which lessened the electrical pain, but did nothing for the cold burning pain or the deep bone pain. But it wasn't just the severe pain that motivated me to get LDN anyway I possibly could, but my unruptured brain aneurysm. I felt that I had to attack CRPS so that I could have brain surgery.

Now that I can walk with a cane I have scheduled an appointment for a second opinion with a top neurosurgeon. LOL It was easy peasy to see any number of stellar neurosurgeons, but finding a good CRPS doctor to give me LDN-forget about it!