I think it depends on the Dr. I get more , better care from my pcp then I did from my rhuemotolist and pain management. Right now I only see my pcp every 3 months. He keeps me stocked up on medication and gives me shots whenever I need it. Hugs and Prayers

A rheumatologist diagnosed (finally) me. I have never seen a specialist. My PCP is wonderful and I believe she knows enough to have informed compassion. My head trauma also messed up my brain chemicals. For 17 years I farmed the pharm--told I'd never function without pills. I stress to all--be proactive in your pharmaceutical care. I was late to the game on that one.

I see a Rheumatologist for fibro. I am seeing an integrated medical doctor next month. They help heal the body as a whole not just a symptom. Looking for her to help me with supplements and see if I can go a more natural route in dealing with the fibro. It took me a while to find her as we did not have one in our area until recently. I see my PCP for regular issues and Celiac.

I see a pain management specialist for my treatments. over the years I had primary care doctors prescribe medications. I also see a physical therapist (at my own request) and try to research as much as I can on the condition to benefit myself. Knowledge is power.

Soulshine. In reference to the pain patches. I alternate for the best results with patches and topicals. My Dr. prescribes me Lidocaine patches 5% at first now 10%. I also use Rx topical pain cream called Difleconac. Both effective. I also like topical creams with Arnica and Topricin. CBD also has a topical ointment with eucalyptus that is awesome. I may still have pain but it is dull vs severe. Sometimes even pain free. Along with sublingual CBD. For the PTSD the CBD oil and a beta blocker is what I am curently on. I have bad panic attacks due to the death of my daughter. I can take it as needed and it's non narcotic. I had to find my accurate dose. But it really works for me.
Hope this helps 🙂