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Any IC or UC people here? (Original Post) Peregrine Took Dec 2011 OP
Me! kdmorris Dec 2011 #1
I have UC but I seem to have bouts of IBS a lot lately. Peregrine Took Dec 2011 #4
My husband suffered from Severe Ulcerative Colitis for many years. Every auntAgonist Dec 2011 #2
Those change of season times can really affect you when you have UC. Peregrine Took Dec 2011 #3
I'm scheduled for the potassium test to determine IC graywarrior Dec 2011 #5
Different but related Lindakimy Mar 2012 #6

kdmorris

(5,649 posts)
1. Me!
Wed Dec 14, 2011, 09:43 PM
Dec 2011

And... sometimes, I think I have IBS, too (the pain is excruciating sometimes.) I know that stress causes flare-ups, but there are days when I just can't calm down.

Peregrine Took

(7,417 posts)
4. I have UC but I seem to have bouts of IBS a lot lately.
Thu Dec 15, 2011, 12:26 PM
Dec 2011

If I eat something that rubs my colon the wrong way or stress - I get terrible cramps or just aching in the middle of the night.

I just got a lightbox - I'm hoping it will help me deal with the latter and SAD issues, too.

auntAgonist

(17,252 posts)
2. My husband suffered from Severe Ulcerative Colitis for many years. Every
Thu Dec 15, 2011, 01:46 AM
Dec 2011

fall and late spring he'd have a horrible flare up. Stress (I always thought) was a huge factor.

He had surgery last February to remove the entire colon and had an ileostomy until June of this year when they did a 'take down' and reversed it. It's taken a while for him to fully recover and he still has some toileting issues but all in all he is SO much healthier. NO flare up this November/Fall .. no bleeding, no pain, nothing ...

Please take care of yourself !

aA
kesha

Peregrine Took

(7,417 posts)
3. Those change of season times can really affect you when you have UC.
Thu Dec 15, 2011, 12:21 PM
Dec 2011

My husband and I BOTH have it! Thankfully, we have a great doc and do acupuncture, too, so we have been in remission for years.

graywarrior

(59,440 posts)
5. I'm scheduled for the potassium test to determine IC
Fri Dec 30, 2011, 09:19 AM
Dec 2011

Decided not to take that route. Too invasive and docs don't care enough to ask why I feel that way. My prescription for myself? Chill. Seems to be working.

Lindakimy

(19 posts)
6. Different but related
Sat Mar 24, 2012, 10:28 PM
Mar 2012

I have Crohns. I was diagnosed in 1980 but had the symptoms for years before that. The doctors spent about 10 years telling me it was all in my head. I had surgery in 1980 that left me with a short gut and a lot of symptoms but did interrupt the misery somewhat. I have learned to live with it for the most part. I've only had one hospitalization since 1980 and don't take any medication on a regular basis. I do have pain and potty problems a lot but, to me, it's normal. Other people have allergies or arthritis...I have diarrhea. Big whoop.

Over the years I have learned what to eat to keep things calm and what situations cause problems - at least for me - and I'm happy to talk with others who are dealing with this mess so they can benefit from my experience if it applies in their case. And I'd love to learn from them what they have figured out. I don't know anybody personally who has this problem. I do think we are all different and what works for me may not work for you. Still...it can't hurt to know that somebody else is going through much the same.

Latest Discussions»Support Forums»Chronic Health Conditions Discussion and Support»Any IC or UC people here?