- Joined
- Jan 18, 2014
- Messages
- 81
Hi
short story :
I'm 35,
14 years ago (I was 21) I was operated for an intestinal perforation (caused by Crohn's disease). Never had any symptom before, and then I learned I had Crohn.
I was fine for a 1-2 years and then I started to have abdominal pain, it was sooo painfull, unbelievable, (König's syndrome, incomplete bowel obstruction) happening once every month (at start). However they couldn't see anything in all the radiography exams. Until it started to be worse and then they saw the stenosis...many years later ! Thank God ! Everything I was eating was blocked.
I was 28 for the second surgery. Ileo-cecal resection. (it was almost a complete obstruction)
Now the last 7 last years were awesome, no symptom, everything was fine... no drug (I do not tolerate the immunosuppressive drugs). And now Crohn is back, I lost 21 lbs in the last 2 months, nauseas, diarrhea, partial bowel obstruction symptoms.... I'm starting to have another stenosis (according to my last exam).
I'm back on Entocort and my Dr wants me to pass another exam soon (MRI or CT) and he told me that if the stenose is still there and short, they could use an endoscopic balloon dilation.
Anyone have passed through this ? is it painfull ? is it working ? What should I expect ? anyone has a story to share about this ?
thank you
(english is not my first language sorry for any mistake)
short story :
I'm 35,
14 years ago (I was 21) I was operated for an intestinal perforation (caused by Crohn's disease). Never had any symptom before, and then I learned I had Crohn.
I was fine for a 1-2 years and then I started to have abdominal pain, it was sooo painfull, unbelievable, (König's syndrome, incomplete bowel obstruction) happening once every month (at start). However they couldn't see anything in all the radiography exams. Until it started to be worse and then they saw the stenosis...many years later ! Thank God ! Everything I was eating was blocked.
I was 28 for the second surgery. Ileo-cecal resection. (it was almost a complete obstruction)
Now the last 7 last years were awesome, no symptom, everything was fine... no drug (I do not tolerate the immunosuppressive drugs). And now Crohn is back, I lost 21 lbs in the last 2 months, nauseas, diarrhea, partial bowel obstruction symptoms.... I'm starting to have another stenosis (according to my last exam).
I'm back on Entocort and my Dr wants me to pass another exam soon (MRI or CT) and he told me that if the stenose is still there and short, they could use an endoscopic balloon dilation.
Anyone have passed through this ? is it painfull ? is it working ? What should I expect ? anyone has a story to share about this ?
thank you
(english is not my first language sorry for any mistake)