# Gastrointestinal issues

**URL:** <https://discussion.livingwithpsoriaticarthritis.org/t/gastrointestinal-issues/2676>\
**Category:** General\
**Created:** [December 3, 2013, 12:17am UTC](https://discussion.livingwithpsoriaticarthritis.org/t/gastrointestinal-issues/2676 "2013-12-03T00:17:25Z")\
**Posts on this page:** 1\
**Page:** 2

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**Author:** ![GrumpyCat](https://sea1.discourse-cdn.com/flex019/user_avatar/discussion.livingwithpsoriaticarthritis.org/grumpycat/32/969_2.png) [@GrumpyCat](https://discussion.livingwithpsoriaticarthritis.org/u/GrumpyCat)\
**Post date:** [December 4, 2013, 7:24pm UTC](https://discussion.livingwithpsoriaticarthritis.org/t/gastrointestinal-issues/2676/21 "2013-12-04T19:24:59Z")

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Night sweats could also be a side effect of medications. There are certain meds that do that to me. I have this often, or the extreme opposite...freezing and can't get warm.

I have IBS. First, I had endometriosis and had my uterus out. I felt better for a while and then the symptoms started to reemerge. Went to GI, did all of those exciting labs, CT scan, exam, sono, etc. Then she put me on the FODMAPS diet. I really did not like what my GI had to say, so I ignored her recommendations for a while, but finally figured out that if I followed the diet, I felt loads better. I try to be a good girl and follow it about 95%. That ain't so bad. Its kind of nice to have SOMETHING that I can treat without a medication.

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