A question or two to experienced Rituximab-ers, please. Thank you to those who replied before when I first had my duo in April. Your help was fantastic and put my mind at rest. This week is my routine review tomorrow but they did not do B Cells in October for my previous bloods review and the rheumy nurse said something then about them coming back a bit, but my ESR and CRP still very good but said they probably would not do them again until a year had passed by?? So that means I had them done in April twice .. before and after infusions and in early October. Don't they need to test B cells every three months or is it done six monthly after a certain time?
I wondered what is the norm for testing B Cells as one rheumy said they didn't alway tell them very much??
(I haven't had tell tale signs of swelling/red hot joints of other out of control RA symptoms .. my fingers are always the first to puff up but have behaved so far.) I did feel late November there was evidence of things feeling in decline a little but had a cold so thought it was a bit of a flare. Still can't make my mind up as the cold gave me a lot of painful joints and stiffness. Then I got a flu virus in December which lasted three weeks. Will find out my latest bloods results tomorrow.
Next question ... do you find your repeat infusion time settles down to an average length or can it vary? .. I know it says on literature the average is 6-9 months and I have gone nearly 10. The thing I find hard to handle and mentioned this before is that you seem to have to go downhill on this med before the hospital take notice and you are then left waiting to get a slot for the infusions which can take up to six weeks. I hope I will never be left in a state of being between meds with nothing to cover me again. That took me so low last year, and I cannot express enough how bad it was. Do you generally follow a pattern or can some people be six months one time then nine months the other? I know a couple of my rheumy's patients have gone 12 months which is more rare but excellent for them.
I also read that the second duo pf infusions work better. Is this so had anyone found? Do the B cells deplete any quicker on a second duo of infusions? Sorry if this sounds daft but it was something I heard and thought strange.
Many thanks, as I know I won't get much chance to discuss the med tomorrow as there are other things such as podiatry and blood tests to talk about as priority.
NK