Methotrexate stopped working ?

I started methotrexate 4th June 15mg (6 x 2.5mg tablets per week) . it took roughly 2 months to take effect and for about a week or 2 fingers were back to normal-ish. Since then they have gradually been going back to the way they were before starting the medication eg. stiff, swelling and painful. im finding it really difficult to clench a fist and cant grip heavy things without dropping them.

anybody else had this happen and what did you do/change?

specialist nurse said if these didn't work it looked like starting the biological stuff.

Is humira injected or is it tablet form??

My fingers are always worse first thing in a morning generally getting abit better throughout the day although never fully being pain free. I believe humira cant be used if you have liver problems ? And although i never have sincey last blood test i have got elevated liver levels. I m having another blood test tuesday to see of they have come down or not. So if they haven't i think i will probably be taken off mtx but not 100%. I will ask my rheumatologist about humira though so thanks for your reply :)

does it hurt when its injected?

I have done some research and it wont be given if you have liver problems :/

which I don't normally have, its just since I have been on methotrexate so hopefully ill find out after 10th Sept if its gone back to normal or not.

thank you.. I wish you well too.