I won't write my whole saga, just to say my GP is thinking I have fibro and CFS, after first him and a specialist suggesting it was psychological of course!
Possibly I do have fibro and CFS, but I feel everything is more indicative of RA. Except for inflammation markers in my blood work.
On the day of my most recent lot of bloods, my nurse (Dr was away which is good because I am NOT a fan), felt and noted obvious joint swelling, stiffness and restriction in my hands, yet the CRP blood work still came back with no indication of inflammation! They didn't recall for ESR this time so CRP is all I have to go on. But of course this rules out Rheumatoid arthritis. My questions are, those of you who are diagnosed with Fibro, what do your inflammation markers look like? Positive, normal, negative? And have you any sign of positive RhF in your bloodwork?
What are your Ferritin levels like?
Have you had all the key body points of pain examined?
I am just sick of flare ups debilitating me, sick of being treated like I know nothing and am crazy, that my bloods are false positives and not being examined as I'm under the impression I should be in order to make a definitive diagnosis.
Any thoughts or info would be much appreciated 🙏💚