Thanks for the response. I think the first main priority was to get my broken bone healed. When that happened then they started focusing on the excess symptoms. I just felt like the neurologist wasn't listening to me and immediately rode off CRPS in general. Like he was insisting it couldn't be that right away. When I do research myself I have all the classic symptoms, just not to the severe magnitude of some people. Like is it common the longer you have it the worse it gets? I'm so young. Should I get diagnosed? Because I can live with the symptoms but they are there.