Hey,
So it's coming up to a year of having infliximab infusions at 8 week intervals. Iv just been told I'm unfortunately starting to develop antibodies. My Dr has said once they have done so more tests and colonoscopy they will have a better idea of the next step - shorter intervals or a new med. I'm just curious of what others have done? I was quite reluctant to start the infusions but they convinced me with the explanation that it was the best possible approach with how my Crohns was presenting. Obviously this is now making me wonder if a new medication will be less effective, especially as I was responding really well. Also currently taking 6mp, allopurinol & pentasa. Like I said just curious of what could happen (in the UK, if that makes any difference) and also did anyone feel any side effects from developing antibodies, I definitly didn't get the same boost I usually do but I had figured that was just life!!
Thanks for any input.
So it's coming up to a year of having infliximab infusions at 8 week intervals. Iv just been told I'm unfortunately starting to develop antibodies. My Dr has said once they have done so more tests and colonoscopy they will have a better idea of the next step - shorter intervals or a new med. I'm just curious of what others have done? I was quite reluctant to start the infusions but they convinced me with the explanation that it was the best possible approach with how my Crohns was presenting. Obviously this is now making me wonder if a new medication will be less effective, especially as I was responding really well. Also currently taking 6mp, allopurinol & pentasa. Like I said just curious of what could happen (in the UK, if that makes any difference) and also did anyone feel any side effects from developing antibodies, I definitly didn't get the same boost I usually do but I had figured that was just life!!
Thanks for any input.