Crohn's Arthritis?? or Reaction to Humira?

In October, I started having extreme pain in the shoulders, wrist, hands fingers, hips and back. Call the GI guy, thinking it was a reaction to the Humira. I reacted to the Remacade after 3 treatments and had to go on high does of steroids on a 6 mo taper. Had no knuckles any more due to the swelling. Couldn't lift my arms up over my head. Having trouble lifting my legs up to get out of the car. The GI guy said he didn't think it was from the Humira and not stop it and to see my GP. Thinking it could be gout or some other manifestation. After 40 min. with the GP. He wrote a script for a Medrol dose pack. In 3
days everything was gone. All pain, swelling, and range of motion returned. I had knuckles on my hand. Made it through till the last pill of the dose pack and everything started coming back. The pain, swelling, etc. Within a week, I was back to where I was before. I had some prednisone I use for my dogs allergies, so I took that and stopped the Humira. Everything disappeared again, made it through Xmas. Tapered off the Pred. and symptoms came back again, even off the Humira. Couldn't get in to see anybody due to Xmas, finally got into the GP, who said I needed blood test, xrays, and to see a Rheumatologist and my GI guy. Got into the GI guy after the xrays and blood tests and he said I have an Inflamatory Arthritis condition maybe due to the Crohn's or the Humira. Stop the Humira, and get by until I can see the Rheumatologist. I just started a new job the day after I saw him, and had to make it through the day, so back to the dogs Prednisone. I made it.
They called today with the appointment for March 14th. Percocet doesn't kill all the pain, nor give me range of motion that I need to perform my 4 hr a day job. I wouldl like a little input how to deal with this situation. HELP!!

I began experiencing serious joint/muscle pain which I noticed when I was late taking a Humira dose. I recently stopped taking the meds and the pain is now chronic. I feel that the Humira induced the problem and have done some significant surfing of the net to find others who have reported the same issue. I am currently waiting for bloodwork results testing for ANA (Lupus) and other inflammatory markers to determine if there is any actual sign of arthritis. I find it frustrating to be told that it's 'normal' as a crohn's patient for me to develop arthritis while my instincts tell me that the onset of these symptoms is directly related to having taken the Humira. I feel frustrated and scared. I have always been incredibly active, done physically demanding work, walked everywhere without owning a car and never had an ache I couldn't directly associate with an activity that caused it. Three weeks after stopping the Humira for good, I starting falling into bed at night in agony, felt like 110 in the morning, couldn't lift my arm without excruciating pain, had swollen thumbs and hands, pain in wrists and forearms, felt like I blew out my knees, soles of my feel hurt and felt like stakes were being driven through my shoulders. I'm praying that whatever changes my body went through as a result of taking the meds, it self corrects. It's is indeed awful and I will continue to push the MDs for answers until I get some.

I can't speak for Humira, but when my son was on Immuran, he developed terrible arthritis in his hips. He could barely walk. He also developed iritis. Both conditions were attributed to the Crohns, but within days of stopping Immuran, he started to feel better, and within two weeks, all signs of arthritis and iritis were gone, and haven't been back in over three years