Had to go to my GP after blood pressure tests showed high reading during My last infusion. The dr decided to do some blood tests. One was repeated twice and showed that I was severely anaemic. Other tests have been ok. He thinks that it is the sulphasalaziene causing it as it is one of the side effects. He has now put me on medication to correct it and I have to go back in January for another blood tests to check I am now absorbing the iron. I am feeling heaps better and find I can do a little more without being so tired. I still have to pace myself. On another note my fingers have started spreading and the physio has given my a contraption to wear in bed. Problem is I cannot get used to and my arm from elbow to hand is immobilized with it. Hey no, the joys of RA.