I was diagnosed about a year ago. At the time, the pain and swelling was limited to my hands. I was on Enbrel for three months to no avail. The pain progressed to my back and I was put on mtx and inflectra, which i have been on for about 7 months with fairly good results. the most debilitating part of RA had been the several episodes of debilitating fatigue that completely derailed my life and would last anywhere from 2-3 weeks. about two weeks ago my feet began to hurt. i saw my rheumatologist and had cortisone injections which really didn’t help. the pain has been incredible and inescapable. i have to had to use crutches a number of times just to make it from my couch to the kitchen. i have been eating pain medIcation like candy (though managed to get through today without any!) i cannot walk my dogs, exercise, etc. while my hands were also incredibly painful, i didn’t have to use to them to get places!!! i guess what i am trying to determine is if this is what a traditional flare feels like, or is this a sign that the disease is progressing and the medication Is not working. i know from my MRIs that the RA is particularly corrosive and from i have been told can be tricky to treat. i am zero percent ready to use canes and/or crutches permanently. can anyone shed any light on what i might expect, or has anyone had similar experiences? i am picking up my handicap placard tomorrow–let’s hope i don’t have to renew it after 6 months!!! THANK YOU!