- Joined
- Jul 19, 2015
- Messages
- 12
Hi there,
I have had been diagnosed with Crohn's Disease around a decade ago. I have had two major flares in that time frame. Currently, I believe I am going through my third. It seems like the pattern is around every four to five years that I get a bad flare and typically have to try new medications. Currently the past four years I have taken Humira alone and that has always helped.
About three months ago I was working out, and started getting very painful pains in my abdomen. I had thought I had pulled a muscle. Went to the ER, they said I strained my abdominal muscles. For a month I struggled with the strain, but the pain didn't go away, and my GI wanted me to come in for a CT scan. I had a CT scan and they found an intestinal abscess in my Terminal Ileum, coupled with inflammation which was narrowing my passageway.
Per that discovery, my doctor put me on CIPRO and FLAGYL to treat the abscess. Those two medications destroyed me. Told me to go off of them, had another CT scan done, found that the abscess was healing if not almost gone, and that inflammation has gone down a substantial amount. He also did an endoscopy to see if I had an ulcers in the top of my GI tract, and also did a biopsy for H. Pylori, they found nothing. The GI said that he believes the Humira isn't working and wants to get me started on Entyvio. I start that in the next few days.
I sat down and really thought about things, and my symptoms haven't been typical to what I know. Usually, I have diarrhea, severe weight loss, general sickness, and lack of energy. But they are different this time. This time, I noticed that when I eat food, within ten minutes I am having severe abdominal pain, and I seem to burp a lot. From what I feel, it's like when I eat, I have an insane amount of gas that just doesn't escape. I have bowel movements that can be comparable to that of a person without Crohn's Disease. All of which is so different and odd.
I am curious. Does this sound like stricturing, inflammation, or an abscess/fistula to anyone here? I am taking a low dose of Prednisone at 10MG for the past two weeks or so. But I don't feel like it's doing too much.
Has anyone experienced this? What are your thoughts?
Thank you so much!
I have had been diagnosed with Crohn's Disease around a decade ago. I have had two major flares in that time frame. Currently, I believe I am going through my third. It seems like the pattern is around every four to five years that I get a bad flare and typically have to try new medications. Currently the past four years I have taken Humira alone and that has always helped.
About three months ago I was working out, and started getting very painful pains in my abdomen. I had thought I had pulled a muscle. Went to the ER, they said I strained my abdominal muscles. For a month I struggled with the strain, but the pain didn't go away, and my GI wanted me to come in for a CT scan. I had a CT scan and they found an intestinal abscess in my Terminal Ileum, coupled with inflammation which was narrowing my passageway.
Per that discovery, my doctor put me on CIPRO and FLAGYL to treat the abscess. Those two medications destroyed me. Told me to go off of them, had another CT scan done, found that the abscess was healing if not almost gone, and that inflammation has gone down a substantial amount. He also did an endoscopy to see if I had an ulcers in the top of my GI tract, and also did a biopsy for H. Pylori, they found nothing. The GI said that he believes the Humira isn't working and wants to get me started on Entyvio. I start that in the next few days.
I sat down and really thought about things, and my symptoms haven't been typical to what I know. Usually, I have diarrhea, severe weight loss, general sickness, and lack of energy. But they are different this time. This time, I noticed that when I eat food, within ten minutes I am having severe abdominal pain, and I seem to burp a lot. From what I feel, it's like when I eat, I have an insane amount of gas that just doesn't escape. I have bowel movements that can be comparable to that of a person without Crohn's Disease. All of which is so different and odd.
I am curious. Does this sound like stricturing, inflammation, or an abscess/fistula to anyone here? I am taking a low dose of Prednisone at 10MG for the past two weeks or so. But I don't feel like it's doing too much.
Has anyone experienced this? What are your thoughts?
Thank you so much!