Posted 2/3/2010 12:47 PM (GMT 0)
Thanks for responding. I am currently in therapy, cognitive behavioural to be exact, and have been for about 2 years now so I am attempting to get things taken care of and it is helping considerably. I did speak to a Dr. about the malabsorption during my last flare and was told it was probably due to the D, I was just wondering whether anyone else had experienced anything similar. Also I have tried rectal meds, unfortunately they didn't seem to do much either...the only thing that really made a huge and immediately noticeable difference was the cortisone but as soon as I got off of it I was back to square one, even with the mesalazine and the suppositories and enemas...