I'm pretty sure ms is causing me chronic constipation.
I think my intestines are spasming shut, to the point that nothing solid will move through. The food just piles up in my small intestine in the same place right below my brestbone. Basically I eat without pooping for 4-5 days, then I cant take the pain anymore and drink natural calm all day until everything is liquid and flows out. My poop is also pencil thin when I am able to poop.
I've had a ct scan and an sigmoidoscopy and everything was unremarkable. I was not having symptoms for both of these. The prep for both basically puts me into remission. When it first started happening, I got weird tingling/thightness in my chest, along with intestinal pain. That's what pointed me towards ms. The tightness directly correlated with the constipation and my 100 other symptoms. I always describe it like my poop is pushing on a nerve in my intestines. It's full time now, with rare relapses for a day or two.
Has anyone else had this issue? Did any medications work?
I've tried reglan and Im currently taking muscle relaxers. Please dont say fiber, water, etc. I've tried them all. Most of them make it worse as bulk appears to be my main problem. The reglan appeared to work for a few days, but seems to be doing nothing now. I'm trying flexaril now, but it does not seem to be helping yet.
Are there any tips or tricks you guys use? I'm scheduled for an mri on the 30th, but I'd like to get my digestive system working asap and I'm not sure I'll be getting any ms meds anytime soon.