Keep checking back on this board; it is a tremendous resource for all.

As CRPS is a very "individual" condition, we'll provide lots of support and encouragement, but can only tell you what works for us. What works for you is what you need to discover. There can be a fairly long discovery period with this goofy problem!

Getting under this as quickly as possible gives you by far, the best potential for best results. I had my foot in a camwalker for 3 months before we discovered that mine was CRPS. That was not a good start! We all have our unique stories.

Personally, neurontin (gabapentin) is the cornerstone of my medications. It helps me tremendously. But again, what works for some may or may not work for the other. There is usually some experimentation needed with meds and then with their dosage titrations up and down. I was on percocet for a long time, but didn't like the dependency issue and so I weaned myself off that after about a year (that was not easy, nor fun!)

I have had a lot of trouble sleeping since my diagnosis. What works best for me is some trazadone an hour before bed. Not a lot, just enough to help me sleep. Sleep is so very important to handling chronic pain! Ask your doctor about what might be appropriate for helping you sleep. A reasonable nights sleep makes the next day seem much more tolerable.

Keep good records in a notebook or on your computer so you know where you've been with all of this.

Good luck!