Before I put my bit just want to say what wonderful news Jean's shared with us all, must be so reassuring to those of you who are really struggling to know that things can get much much better, just got to have faith and never give up hope.
I knew most of Jenni's story and I have nothing but admiration for her. She's always seems so positive and never gives up. I have been looking on here most of yesterday and today looking for news of her appointment yesterday (8.30 Thursday morning) hoping that something positive came out of it.
Lyn.......well I knew you had had problems but I had no idea that things had been so bad for you. I always look forward to your replies on here because you seem to know such alot about various aspects of treatment, I can see why now.
Francesca..........For someone so young, you have really had alot to deal with. Just pleased to read that apart from you hip you are able to do what girls of your age should be doing. You've also given me hope that I may one day be able to wear my 'high heels' again.
Well about me. I was diagnosed 2008 and started on SLZ. Worked very well for a time and then things slowly started to get worse. Little things, nothing major but when I start to compare myself with how I was at my best, I can see a difference. It's like RA is slowly chipping away at me and taking me from me bit by bit.
I now take 6 SLZ a day and 20mg of MTX along with stomach protector, folic acid and slow release brufen based pain relief. It looks like it is on the cards for me to start injecting MTX (been advised by nurse to and I am waiting to see consultant), that way we will be 100% certain that all of the dose is getting in my system.
I've read on some post that pain relief is not needed much, well, me being me and just needing to know, I decided a few days ago not to take any pain relief for the day to see what would happen. The next morning I was in so much trouble. Hard to believe that two tablets could make so much difference. Wondering if its the pain relief that's doing the controlling and not the DMARD's............
So, No I don't think that my RA is under control.
Paula