Posted 2/20/2015 6:12 AM (GMT 0)
I haven't been on here in awhile. I have had CD since 2003, been on remicade since 2011. I am feeling "okay" but not as good as I did a couple years ago. In the last year I have developed joint pain in my fingers, wrists, back. Bearable, but wakes me up at night. Saw Rhuemi, she said inflammatory arthritis related to the crohns. I am more tired, very slightly anemic, occasional diarrhea. Don't know if I'm just feeling older with this disease or heading into a flare...! I am feeling really discouraged that the joint pain is now a part of this :( do others get joint pain? What does it feel like for you? What do you find helps? Has anyone tried Curcumin?, I'm considering it...thoughts welcome!