What a terrible experience for you! I'm glad your Dr is now intervening to get you to people who can properly help you. I've had the same experience of emergency staff unwilling to give pain meds because they think this normal looking man is just an addict. I've learned since that episode to bring my pain meds with me to prove I'm not seeking narcotics.
Before I was diagnosed and even after, I had severe pains in my wrists and hands that no Dr. could figure out why. I even had custom made hand and wrist braces just so I could do my job operating sawmill contol panels. The company even re-built my control panel to my design with light touch buttons so I could work it.
The pain at times was so severe it was like having broken bones in my hands or wrists at times. This severe pain would come and go with absolutely no pattern disernable but other levels of pain were always present. When I was put on prednisone it reduced the pain by around 1/3rd. When I was put on remicade 3 years ago, it immediately reduced the symptoms to maybe 10% of when it was at it's worst and even would go away completely for days at a time. Eventually as I continued on remicade (every 8 weeks) the effects of the remicade would only last 7 weeks then 6, now it only lasts 4 weeks but even when it returns it's at a lower level of pain than before remicade (usually). Unfortunately my government only will allow crohn's patients treatment every 8 weeks. Lately I've been wondering what I can switch to to get better bone pain relief, beyond the 4 weeks. I'm not sure humera does the same for pain but your post make me wonder if Cizma may be what I need to try next. You've given me a little hope, thank you and best of treatment to you Rob