Just wanted to say I'm sorry to hear of your intense pain. I empathize as I suffered for over a year praying every night to please let the pain go away and let me die in peace. All my joints froze on me, had the left side shuffle thing going on. do not know if it was ms related. I'm in midst of diagnostics. My pain was helped by neurotin low dose, but it stopped working last July. I only hope you listen to you body, as I found complete bed rest, and I incorporated a 1 mo juice fast, with a bit of chx or scallops low/no fat regime. (had to as i passed out i was so weak, drs doing nothing) This was opposite of what drs had advised. Keep telling me exercise would either make me better, or I'd get worse without it. I had to fire and walk out on a couple of pt. find a good one to work with, I did. Build u strength back as you feel comfortable. Hope u find a pain med that works for u.. Likely start a über low dose as u can always add. Different manufacturers, same drug, different reactions.

Pardon if Ive rambled.. I wouldn't wish that type of pain on my worst enemy. There's a new pain management treatment, non drug, was offered me but my pm dr said not to. It was 2 hr drive for me so I didn't enlist. Be happy to share info with you if u like. (have to locate email) the natl lyphoma society hooked me up to the procedure. My reg drs rot.

Do hope you find relief soon. Kat