Just realised I hadn't posted anything about myself! I was diagnosed in 2000 after a almost a year of misdiagnosis. I lived in Scotland when diagnosed and was put on sulphazaline which I supported for a few years. Moved to France (Picardie) in 2003 and have several major flares and drug changes since (Leflunomide, Methoxtrate, Enbrel, Abtacept, Tocilizumab) - some due to secondary effects/allergic reactions, and some to the fact that the drug didn't do a lot. Last year, after discovering that the bones in my right wrist were fussed (therefore other treatments weren't working) was put on Rituxan (by infusion in a clinic every 6 months). Apart from feeling exhausted all the time, everything is going well but can't wait for the sun to shine this year!