I’m interested to hear, from those of you who have RA, (a) did you have to stop taking the medication before, during and/or after the surgery, and on whose advice - rheumatologist or surgeon; and (:thumbup: has the RA improved or worsened since surgery?
I am on methotrexate and prednisone (steroids), plus sleeping tablets to help me sleep through the pain at night, and find if I don’t take my medication at about the same time every day, within a couple of hours I am in considerable pain - so I am not looking forward to a few days (?) without the medication, if that is what it takes.
I realise these are questions I should really be asking my rheumatologist and the WLS surgeon, but I now live in France and, although my understanding of French is reasonable, putting these questions is a bit beyond me!
I see the surgeon on Thursday morning, and knowing what the French health system is like, I’ll probably be banded within a matter of days, or a couple of weeks - they don’t hang about here!