6 years after after my first ever flare, having seen 4 nurses, 3 consultants, Prescribed MTX (25) and sulfasalazine, with no change and more frequent and severe flares, I am awaiting my delivery of Humira!
My local hospital has taken on a new consultant and I was placed under her watch. After our first consultation she ticked all the boxes for me to be eligible for biological therapy and advised it should have been sooner as I meet the conditions. God is the source of strength
The reason I am posting this, and it's not the first and may not be the last time it is asked, what is everyone's experience with Humira as the biologic nurse she thinks fortnightly injections would be best for me.
I'm so happy yet in the back of my mind I know it may not work. Any info would be much appreciated