I'm 43 and have had Crohn's since I was 14. From 19-25 was the worst: one resection, another one while I was pregnant at 30. Been in remission or so I thought. Iron deficient and low blood counts for five years and guess what? Turns out it was Crohn's the whole time only it could only be diagnosed with the single balloon enteroscopy. Another resection March 2010. Things were great then same ol' symptoms: cramping, diarrhea, constipation, pain, bloating etc.
Seeing a new doctor who wants all new tests. Even though I have repeatedly told all of them (and shown them my records) that my disease is only at the site of my resection (small bowel--near where terminal ileum used to be), they insist on putting me through the same round of testing: Scheduled for upper endoscopy/colonoscopy in two weeks. I'm very nervous about
the prep after the horror stories I've read (miralax/dulcolax). Also very depressed that I'm dealing with this once again.
Thank you all for letting me vent. Pretty much had enough at this point.