I am about to start Humira and am keeping everything crossed (well if I could actually physically cross stuff I would! ) that it will be the one that works for me.
I am guessing that most of my pain is from the inflammation of the RA attacking my joints and when the Humira starts to work the pain will reduce. I know my knees (especially the one that has had a TKR twice) may never be pain free, but I wonder mainly about my shoulders (elbows, wrists and hands next in line!). I've never had any joint damage diagnosed but they are quite crunchy when I move them as much as they move - what have other people experienced when they find a medicine that works - or am I back to the 'everyone is different' and RA is a progressive disease and ever changing differently for everyone!
I am really trying to be positive but being a bit of a control freak and needing to know everything I am finding the fatigue and unpredictability of RA the most difficulty things to deal with!
Thanks for such a great forum and NRAS you are really keeping my going!