You may remember from a post a week or so ago that OH, after appearing to respond well to MTX two months in, went sharply downhill. It seemed like it had just stopped working. The joint pain, fatigue, flu type symptoms etc came back as bad as pre treatment and have just been getting worse.
After speaking to the rheumatology nurse, he's going to be switched to MTX injections. I thought this was only done if you got digestive problems on the pills, but apparently in some people it can just work better. Does anyone have this experience?