I have gone through the “let’s rule these things out” process with my PCP. I am now on thyroid meds and using a CPAP, but my symptoms persist. I have had imaging test done, but nothing found to explain the pain (no MRI yet).
So I received the, “It sounds like Fibromyalgia.” I don’t have the tender spots that I believe are associated with Fibromyalgia. I took it upon myself to explore further. I made an appointment with a neurologist.
I have anxiety over waiting two and a half months, for a 40-minute appt, to be brushed off. I cannot stop thinking about, “Will he listen, will he actually listen to all I am saying?”
How do I get my mind to quiet down and trust in the process?