New Topic Post Reply Printable Version
[ << Previous Thread | Next Thread >> ]

TP1986
New Member


Date Joined May 2010
Total Posts : 19
   Posted Today 6:27 PM (GMT -6)   
Has anyone had any issues from eating oatmeal?

I'm watching the foods I eat to see if anything makes things better or worse looking for good breakfast foods

Malkavian
Veteran Member


Date Joined Mar 2009
Total Posts : 1439
   Posted Today 6:36 PM (GMT -6)   
Oatmeal sometimes increases volume for me but not much else.

For breakfast I like egg on toast. Eat that all the time when flaring.
Heather, 22/Female/NJ
Ulcerative colitis from rectum to mid transverse colon, diagnosed 3/6/2009, symptoms for 2 years beforehand
Remission?!?!?!
Currently on lialda 4x/day, azithioprine 150 mg/day, calcium and d, B12. Enemas make things WORSE
Allergies: penicillin, sulfa, bee stings, environmental (especially ragweed!), OTC meds as needed


LeafsFan
Regular Member


Date Joined Dec 2008
Total Posts : 274
   Posted Today 8:36 PM (GMT -6)   
Oatmeal works for me - just make it soft
Chuck - 29 yrs and counting
 
Diagnosed w/ UC Dec 08 - pancolitis
 -----------------------------------
Pentasa 4000mg daily, 150mg Azathioprine can't take - had low white blood cell count
Prednisone   Calicium + Vit D
Vitamin B12, probiotics, fish oil, Iron Supp.
 
"If you can solve your problem, then what is the need of worrying? If you cannot solve it, then what is the use of worrying?"


Old Hat
Veteran Member


Date Joined Feb 2007
Total Posts : 5064
   Posted Today 9:31 PM (GMT -6)   
Pillsbury farina works best for me in flares or right after scopes. Usually I do o.k. with slow-cooked oatmeal, though. / Old Hat (30 yrs with left-sided UC; presently in remission taking brandname Colazal)

Ugh Just Ugh
Veteran Member


Date Joined Jan 2010
Total Posts : 1004
   Posted Today 9:45 PM (GMT -6)   
I do well with oatmeal but as Old Hat said, the old fashioned kind. The instant packet ones that have flavors and stuff are too sugary. Lately my go-to breakfast has been yogurt and a banana.
Jennifer
Originally Diagnosed: 7/08 Mild left sided UC
Current Flare started 12/26/09: Severe Inflammation through Entire Colon, some patchiness indicates might be Crohn's.
Current Meds: Prednisone 20mg (Trying to taper again!), Imuran 150mg, Apriso, Lexapro (5mg), Xanax (.25mg) as needed.
Past Meds: Mesalamine Enemas, Canasa Suppositories, Hydrocortisone Enema & Supp.
Supplements: Multivitamin, Fish Oil, C, Iron, D, Calcium, Potassium, Bio-K, Primadophilus Reuteri.


bikegirl
New Member


Date Joined May 2010
Total Posts : 8
   Posted Today 9:53 PM (GMT -6)   
oatmeal has phytic acid which blocks absorbtion of trace minerals... your best bet is to soak it over night with something like a TBSP full of lemon juice or vinegar. Just place oatmeal water and lemon juice or vinegar in a pot, cover it and let it sit on the counter overnight. When you wake up rinse it a little (if you want you don't have to) and cook it. This helps eliminate some of the phytic acid so you can get as many trace minerals as possible from your meal.

Lynn4221
Regular Member


Date Joined Jan 2010
Total Posts : 195
   Posted Today 10:22 PM (GMT -6)   
Oatmeal puts me right onto a lot of mucus-
I tested as highly reactive to oats in a food sensitivity test-
L
UC dx in 2008
4g Mesalamine nightly
Healthy Trinity x4/daily
Nordic Naturals Ultimate Omega x2/daily
Curcumin Plus
Following Ageless Nutrition Colorectal Recovery Program x 4 months


quincy
Elite Member


Date Joined May 2003
Total Posts : 28934
   Posted Today 10:29 PM (GMT -6)   
oatmeal gives me discomfort and gas...I'd never see it as a comfort food regarding digestion. I love it, however....

It won't hurt your disease, try an egg and toast...save the oatmeal for a night-time snack if you want it.

q

TP1986
New Member


Date Joined May 2010
Total Posts : 19
   Posted 5/27/2010 6:26 PM (GMT -6)   
Thanks for all the help :)

subdued
Veteran Member


Date Joined Dec 2008
Total Posts : 3231
   Posted 5/27/2010 7:53 PM (GMT -6)   
It depends on what is in the oatmeal. Oatmeal, itself, doesn't give me any issues.
Colitis is in remission. No longer get IBS.
 
Figuring out how to reduce a flare or get into remission is a trial and error experience. Don't expect your GI to have all the answers. He was trained in making diagnoses, prescribing medications, and surgically removing the colon. He was not trained in alternative treatments. That's why they are called alternative treatments.

What works for me: Fecal transplantation, Probiotics, Anti-inflammatory foods, No HFCS, No crystalline fructose, No foods high in fructose, No artificial sweeteners, No pro-inflammatory foods when flaring, vitamins & supplements, Lexapro (for stress).

New Topic Post Reply Printable Version
Forum Information
Currently it is Friday, May 26, 2017 8:26 PM (GMT -6)
There are a total of 2,815,715 posts in 309,151 threads.
View Active Threads


Who's Online
This forum has 151616 registered members. Please welcome our newest member, KClp88.
405 Guest(s), 9 Registered Member(s) are currently online.  Details
DBwithUC, Lioness1, Klagh, PeterDisAbelard., Lilianna Rose, Joe183288, Fletch10, Pratoman, anass


Follow HealingWell.com on Facebook  Follow HealingWell.com on Twitter  Follow HealingWell.com on Pinterest
Advertisement
Advertisement

©1996-2017 HealingWell.com LLC  All rights reserved.

Advertise | Privacy Policy & Disclaimer