Wow thanks so much everyone for that information. What puzzles me is that my Rhuemy told me that there was NO treatment for the AS and as I have found out there are some drugs like Enebrel (excuse if I mis spell any drugs etc being new). Now I am realising that this drug is approved but that is so expensive that is very disillusioning, cruel infact. As I understand it you have to have certain markers or levels of something toi qualify for assistance with insurance or government subsidisation. I am kind of cross he never told me about this drug but is willing to put me on chemo drugs! Thanks for confirming too that this Methaltrexate isn't really an answer to the AS which for me is far worse than my Psoriatic Arthritis. I might get a second opinion and just have to stay in my drug haze for now.
Thanks for the welcome and advice/info it is so VERY much appreciated:)
Kaz
There is so mcu to learn here! You are gems....
