Hello AF community,
Once again I seek your insight, advice, perspectives, personal stories....
In the last year or so I've had two fissures (or it could be the same one that re-opened a year later because both are in the same area, posterior region). When I had the second fissure late January of this year I scheduled my first GI consultation and CRS appointment to try to get some help figuring out whether I seem to be susceptible to them.
At my consult the GI's only solid suggestion was to ask the CRS to test to see if I have a high resting pressure or tight sphincter. Later in the day she wrote, "After thinking more about your case, I think you should have a colonoscopy to check for Crohns. Fissures can be an early sign of Crohns."
Later in the day I went to see the CRS who gave me a digital and scope exam and said my fissure is healed and all the tissues look nice and healthy. Her advice seemed to be to see a pelvic floor therapist to learn biofeedback, take Miralax regularly to keep my stools soft, wean off the Colace, and go from there.
I found the GI's rec to get a colonoscopy bewildering since I don't have any symptoms of Crohns. So I asked teh CRS what she though, and she seemed ambivalent writing "It is uncommon to have fissures as the first presentation for Crohn's but she [the GI] would certainly be more familiar with this sort of early presentation. You have had 2 fissures so you could either go ahead with the colonoscopy or give it more time to see if this turns out to be more of a chronic problem."
Just wondering if anyone out there has any advice, insight, perspectives to consider on this choice I'm facing. Perhaps needless to say I'm not enthusiastic about getting a colonoscopy. They do have risks, and I feel like it isn't clear it's worth the risk given my current situation. Thoughts?
Thank you and wishing you all healing.