Is it or isn't it inflammatory?

Hi everyone hope you all are good,

havent been on the forum for a while due to health probs and medical appointments....and fatigue. I am very confused at the moment because all the stuff I have read on fibro so far says that it is not inflammatory yet I have recently went down bad with Costochondritis and have and inflammatory problem in my ear that is causing a pulsing kind of tinnitus. I have left one doctor who tried to say my chest pain was from MY BRAIN and was found out of hours on two occasions to be pretty bad costochondritis. I spoke to a female doctor over the phone two days ago and she told me that fibro is an inflammatory condition :O, after i said i have costo and i thought fibro wasnt supposed to be inflammatory, so why so many sites of inflammation, not even going to talk about the bladder. I have pretty much had it up to my neck and submitted lots of times due to attitude of doctors, ive been getting complicated migraines acting as tias and the doctor i wont be going back to told me medically unexplained symptoms no more testing. Sweet huh.
Like many of us I have hypothyroid and also psoraisis which are both autoimmune in nature and i wondered if anyone who has more knowledge could explain why im coming down with more and more symptoms. Im now referred for a MRI to exclude MS and other causes of neurological symptoms and due to see an ENT specialist. Is this the normal path for fibro? I have never had bloods taken for RA or Lupus and wonder if my full blood count would have shown signals of anything going on. Bloods are fine at moment thankfully. Much much frustrated and confused. Sorry for venting but I am trying to get on top of someething that has had me at its mercy for two years.

Hope everyone else is coping better than me . Hugs

hi sobermommy a tia is transient ischemic attack or mini stroke (reversible) had two episodes within a month, neurology said complicated migraine, had numbness down one side numb tongue and face but idk cos now my ears are starting to rumble and pulse and ive seen menieres associated with fibro so i guess im jumping to conclusions i hope i havent had a tia or have MS but youre right ya know they should have done bloods but they wont im in uk and nhs is all cost effective, i have pain in my hips on awakening and i think its all connected, i had other kinds of chest pain apart from the costo and had treadmll testing and echo done nothing found, fibro is a beast and very challenging

Hugs to you hun ty for replying