Hey guys, sorry I'm late to this post. I've had this for 10 yrs 1 month now. I went to a bunch of Dr's that all said it was in my head and I just wanted a free high. I finally got sent to a PM Dr and he diagnosed me with CRPS type 1. It is a relief to find someone that says you really do have a problem and it's not all in your head or you are just a drug seeker. I've been on Amatryptiline and it caused mouth ulcers, and gabapentin which I didn't have any side effects from. Remember though we are all different, our CRPS is different too. I've been taking 6000mg of Vitamin C lately because I just had a C section 6 days ago and don't want this to spread from my left leg and right knee to my incision site. When I can I will start back on epsom salt soaks but can't till this thing heals. It hurts like the dickens but listen to the advice here and some of it will help you. Not all because mwe are all different. I wish you luck in finding a good PM dr. I will hopefully start back on treatment in January down in El Paso.