First of all, welcome here.

There's lots to wade through, I'm sure; and the way RSD/CRPS is treated varies so much, so so much over the world.

If you haven't gone to a pain specialist or clinic, I would highly recommend it. They *know* CRPS, they aren't "just" there for the pain. That is one big myth.

I had to get over that hurdle myself. Because it feels like you are running out of options, when they actually give you options not to just treat the pain but also potentially treat the condition itself.

I'm thinking bisphosponates for instance.

Anyway, I just wanted to quickly pop in here and say "hi"!

Good luck!!!
& Hang in there!!!

You are not alone in this.