- Joined
- Oct 7, 2016
- Messages
- 2
Hello!
So I’m 53 and had an unexpected Crohn’s diagnosis last year after a routine colonoscopy for diverticulitis – in retrospect I’ve had loose bowels for 30 yrs, a perianal fistula 20 yrs ago and had mouth ulcers, migraines and occasional night sweats during the previous 6 months. I had my first bad Crohn’s flare last Autumn, brought on by the NSAIDS used to treat sudden onset ankylosing spondylitis. Luckily a course of prednisolone brought both conditions under control, although they both started returning in December, a fortnight after stopping the steroids.
I decided to start the SCD diet at New Year and 3 days into it my stools became much firmer and I was only going once or twice a day. However, my mouth ulcers and anal fissure returned a week ago (along with a continued worsening of neck/back pain) so I had my bloods and faecal calprotectin checked. The results are so much better than they were during last year’s flare - CRP only 15 and calprotectin 200 – but the ulcers and fissure not that much better than before.
Do you think my results are less dramatic because of the SCD diet? And why do I have ulcers and a fissure when my diarrhoea has stopped and Crohn’s markers aren’t that high?
So I’m 53 and had an unexpected Crohn’s diagnosis last year after a routine colonoscopy for diverticulitis – in retrospect I’ve had loose bowels for 30 yrs, a perianal fistula 20 yrs ago and had mouth ulcers, migraines and occasional night sweats during the previous 6 months. I had my first bad Crohn’s flare last Autumn, brought on by the NSAIDS used to treat sudden onset ankylosing spondylitis. Luckily a course of prednisolone brought both conditions under control, although they both started returning in December, a fortnight after stopping the steroids.
I decided to start the SCD diet at New Year and 3 days into it my stools became much firmer and I was only going once or twice a day. However, my mouth ulcers and anal fissure returned a week ago (along with a continued worsening of neck/back pain) so I had my bloods and faecal calprotectin checked. The results are so much better than they were during last year’s flare - CRP only 15 and calprotectin 200 – but the ulcers and fissure not that much better than before.
Do you think my results are less dramatic because of the SCD diet? And why do I have ulcers and a fissure when my diarrhoea has stopped and Crohn’s markers aren’t that high?