- Joined
- May 8, 2015
- Messages
- 150
Hi everyone,
So I've ranted on several of the forums here and thought I'd just start a new thread. I'm at the point of losing the little bit of hair I have.
In a nutshell, I was diagnosed with PA fistulizing CD in 10/2013. I had a fistula placed 11/2013. I went on Humira 1/2014 and stayed on it through 4/2015, when I abscessed again. I was switched to Entyvio and 6MP in 6/2015. July the 4th weekend, I developed right lower quadrant pain. Eventually, it got so bad that I was hospitalized for two nights to go on IV steroids.
After being discharged, I was on 40 mg of pred, which was reduced to 30 mg, then to 20 mg, and now to 15 mg. My rlq pain has steadily increased as my pred has been reduced. I had an MR Enterography on 8/3 which showed "questionable mild inflammation" in the distal ileum and moderate inflammation in the rectum. I am scheduled for a colonoscopy on 9/1.
I saw my GI yesterday. He basically said that based on my blood work (normal), my calprotectin fecal sample (normal), and the "mild inflammation", he has no explanation for my continuing pain. The one thing I will say is that he was very understanding and not dismissive. He referred me to another GI in the City for a consult after my colonoscopy.
I'm sorry for the length of this post. I just don't know what to think now. It has occurred to me that maybe I have a conversion disorder. Maybe this is all in my head. Is anyone else dealing with a complete lack of objective evidence to explain their pain? I received the diagnosis. I know I have Crohn's. I know I have some inflammation. Why is it causing this much pain? Thank you for reading.
So I've ranted on several of the forums here and thought I'd just start a new thread. I'm at the point of losing the little bit of hair I have.
In a nutshell, I was diagnosed with PA fistulizing CD in 10/2013. I had a fistula placed 11/2013. I went on Humira 1/2014 and stayed on it through 4/2015, when I abscessed again. I was switched to Entyvio and 6MP in 6/2015. July the 4th weekend, I developed right lower quadrant pain. Eventually, it got so bad that I was hospitalized for two nights to go on IV steroids.
After being discharged, I was on 40 mg of pred, which was reduced to 30 mg, then to 20 mg, and now to 15 mg. My rlq pain has steadily increased as my pred has been reduced. I had an MR Enterography on 8/3 which showed "questionable mild inflammation" in the distal ileum and moderate inflammation in the rectum. I am scheduled for a colonoscopy on 9/1.
I saw my GI yesterday. He basically said that based on my blood work (normal), my calprotectin fecal sample (normal), and the "mild inflammation", he has no explanation for my continuing pain. The one thing I will say is that he was very understanding and not dismissive. He referred me to another GI in the City for a consult after my colonoscopy.
I'm sorry for the length of this post. I just don't know what to think now. It has occurred to me that maybe I have a conversion disorder. Maybe this is all in my head. Is anyone else dealing with a complete lack of objective evidence to explain their pain? I received the diagnosis. I know I have Crohn's. I know I have some inflammation. Why is it causing this much pain? Thank you for reading.