Humira question

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Regular Member

Date Joined Jan 2006
Total Posts : 32
   Posted 9/13/2009 11:18 PM (GMT -6)   
Remicade really worked for me but I had severe reactions and they switched me to Humira. It works but barely lasts a week and then my joints start killing me and though I do not have sever symptoms in my intestines, it sure is not as good as it was. Can anyone else share their experiences with the switch from
Remicade to Humira? Not sure what to do next...... cry cry it's starting to get me depressed again......

Elite Member

Date Joined Sep 2005
Total Posts : 10404
   Posted 9/13/2009 11:22 PM (GMT -6)   

New Member

Date Joined Sep 2009
Total Posts : 1
   Posted 9/21/2009 8:31 PM (GMT -6)   
I have been experiencing severe joint pain all summer. Today it is hard to walk turn over in bed etcc. At times it would effect only my hand. The pain so intense I couldn't sleep. Then it would go away. Week later it would effect my leg, it was a weekly symptom different area. Lately its everything. Scheduled to see rheumy soon. Worried I won't be able to get out of bed tomorrow. I am very active thin, but this is shutting me down. I thought I had lymes disease again or very low in B-12. I actually was low in B-12, had injections helped for a bit then symptoms came back. I have been on Humira 3 yrs, I am  49yrs old. Frustrated  Does any 1 know what is like after not taking Humira, and trying something else.            Peace       Sorry no experience about rhemicaid.

Regular Member

Date Joined Jan 2006
Total Posts : 355
   Posted 9/21/2009 8:54 PM (GMT -6)   
Seattle, how long have you been on Humira? It does take about 3 - 4 months to work. I have more severe GI symptoms and Humira helped me greatly with that. My joint pain was also helped, but was secondary to the GI issues. I went from Remicade to Humira by the way with a pretty big break in between. I sure hope it works for you.

Fhumira, I was on Humira for 3 years before I lost effectiveness to it. Perhaps you are going through that as well? I am now on Cimzia. So far, it is not working at all, but I am being hopeful.

Regular Member

Date Joined Jul 2006
Total Posts : 95
   Posted 9/22/2009 9:48 AM (GMT -6)   
Humira seems to be working pretty well for me though I do think it took awhile to get the maximum effect so if you've just started I'd give at least 2 months.
Solanges: )

Veteran Member

Date Joined Sep 2006
Total Posts : 2527
   Posted 9/22/2009 6:47 PM (GMT -6)   
I have found that I MUST use Humira every week in order to keep both my joints and gut under control however the battle with my Rx insurace is always fun especially when it is time for prior auth or when like now I changed to medicare part D
Dx with Crohn's 1987, symptoms as early as 1984.
Temp iliostomy February 2007, reversed June 2007, Ovarian cysts, migraines, allergies (incl food allergies) , oral allergy syndrome (diff than true food allergies), Asthma, Gall Bladder removed 1999, Inguenal hernia 1987

Regular Member

Date Joined Jun 2009
Total Posts : 354
   Posted 9/22/2009 9:15 PM (GMT -6)   
I'm sorry your suffering right now.
I was on remicade for a year a little and it worked well for the first couple of months, then I started getting servre joint pains. It got so bad I went crippled. it went like this for 8 months, every so often change dosage, 8 weeks, to 7, to 6 to every 4 weeks. WHen finally I decide enough was enough. I had to go through a flush period so I wasn't taking anything, but the doc put me back on Imuran and with in 3 weeks I was pain free from the joint pain, and I could walk with a bounce. I'm not on Humira. The joint pains come and go (doesn't depend on anything, not weather, not if crohn's is flared) but nothing like before, when it does come, I'm still not crippled.
remicade/humira has put my crohn's at bay (for now, not sure of my biopsies result yet)
are you aware these bio meds can cause antibodies? which cause the pain in the joints. Are you taking anything else other then humira
Tracy from Montreal,Diagnosed with CD at age 18 but went undiagnosed for 10 years. 17 years with CD
Remicade for 1 year 4 months. Caused remi induced RA, crippled for 8 months
on humira, working for RA but CD is getting worse everyday,been on humira only 4 weeks
Pantasa 8 tabs a day
Provacede 1 daily for the ulcer's
Imuran 1 and half tabs (50mg)
Previous meds: Pantoloc
                         Predizone, tapered down from 10 pills 8 different times.(horrible side effects)
                         Lots more,list is way to long.
Unable to work last 2 years and counting. Hoping to get my life back soon. Minimum visit's to the ER is every 2 months, to stablize me and send me home. Been 5 years since my last colonoscopy.Got my apointment, Sept 16th. Sooo nervous for the results,in fear the CD has worsen.
Live life to the fullest with no regrets and only eat what you know what hurt you.   

Regular Member

Date Joined Jun 2003
Total Posts : 280
   Posted 9/22/2009 11:40 PM (GMT -6)   
OT, just wondering, did you work at the Seattle Times? My daughter works there now. Bets
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