A few days ago I saw my rheumatologist for bone scan results, expecting to be told there were things up with some of my joints, and maybe be prescribed a new anti-inflammatory, as the last two hadn’t made much difference. What I ended up finding out was that I’ve got a few things up with my joints/bones, but what’s probably been causing my increasingly numerous symptoms these last six months is the fact I have fibromyalgia.
I wasn’t completely blind-sided by this, since I’d looked up the symptoms days ago and myself, my partner, and the friend I complain about my symptoms to all agreed that sounded exactly like what was happening to me. One site in particular made at least part of me pretty certain, as their list of symptoms when fibromyalgia is aggravated covered the rest of my symptoms. The only things holding me back from being completely certain were that I don’t know what is defined as “widespread pain”, and when I tried pressing on the “tender/trigger points” they didn’t feel any more tender than usual (I would’ve used my partner as a comparison, but his pain tolerance is very different to mine). So I thought maybe I didn’t have it, or maybe I was pressing wrong, and went back to rolling my eyes at my partner suggesting a brain tumor as the cause.