After successfully reducing to zero pred last autumn, the symptoms began to reappear. After advice about how to deal with a flare I increased the dose (to 15mg), but that didn't seem to help. Then I was given a depo-medrone injection, with the advice that it would last a couple of months and hopefully clear things up. It lasted two weeks. So, back to 15mg, then after two weeks down to 12.5 and finally down to 10. But nothing seemed to work. I have now been back to the rheumatologist who has prescribed methotrexate, to be taken weekly alongside continuing with 10mg pred. So... any experience/advice about methotrexate would be greatly appreciated. Seems a bit of a dangerous drug, doesn't it? And I am worried about the side effect of mouth ulcers, which I have suffered from most of my life, although not for the last ten years or so. I would hate to get them back on top of everything else. Any thoughts, or personal experience would be very welcome.
Thanks
S