And he has changed my MTX to Sulphasalazine to see how this suits me. He is still not convinced I have RA except for the fact that I have inflammation and swelling in my hands, as seen on the ultra sound scan. My bloods are not showing this, so he says it's sero negative RA, for the moment.
He seems to think that a lot of pain could be due to my fibromyalgia, I have to up the dose of my pregabalin from 150mg per day to 200, I have tried this before up to 300mg, but they just made me a zombie, will try the new dose and see what happens.
It's all getting to me now, the pain is excruciating in my hands, I just can't seem to get any relief. I can't take strong pain meds so I am left with paracetamol. I so hope the Sulphasalazine works for me.
Sorry for the moan, cheesed off with it all