I've been reading all the posts on here, it really is a great place to come
I was diagnosed with RA last summer, and have been finding out more about it and making good progress stabilising on various drugs. It is soooo reassuring to read how everyone else is, their experiences, tips etc. I feel a lot happier and more at peace with my RA since joining the site.
I have been taking MXT orally (amongst other drugs) for about 3 months now, and although I have felt the benefits from it I still struggle with nausea, tummy cramps, fermenting tummy and the 'd' word (that I can't spell!!).
I had a rheumy clinic today and am going to start injecting MXT from Monday. I have a double appointment with the nurse at my surgery. I feel a little nervous, but also quite positive as I understand injecting will most probably help alleviate some of the yukky side effects.
I'm not sure if I am asking a question, or just sharing my mild nervousness! Any hints, tips, positive encouragement gratefully received