Community Forum

Have a question, or want to share your own tips and experiences? Join the discussion in the community forum. You must be registered to participate. Our forums are moderated by Crohn's & Colitis Foundation staff to facilitate a safe environment.

Previous Topic Next Topic

How to tell when a food causes discomfort?

Mon, October 08, 2012 4:09 PM

Hello,

I was recently diagnosed with Crohn's in the terminal illeum about 2 weeks ago. I have an inflamed lower bowel and I'm currently taking Pentasa and Entocort for the symptoms. I've had about 2 flare ups in the past 2 weeks, causing extreme pain in my lower bowel, followed by a fever and fatigue. Since taking the two meds, there seems to be improvement.

I'm still very new to this, so I was hoping for some feedback regarding changes in diet. So far, I continue to eat as normal, without any changes. I don't feel any real pain or discomfort in my lower abdomen while I'm eating, or 1 or 2 hours after finishing a meal. It's more of just a dullness in my lower right stomach that I can always sense.

In terms of going to the bathroom, I don't really have any issues. The abdominal pain makes it difficult to urinate sometimes. Very recently I started having rectal spasms on and off during the day.

I guess I'm wondering if I should just continue to eat as normal until I start having some pretty bad reactions directly following or shortly after a meal? What has other people's experiences been?

kyleb125
Joined Oct 5, 2012

Fri, October 19, 2012 8:19 AM

Reply posted for KyleB125.

I was recently diagnosed with Crohn's.I haven't been back for my follow up appt. yet since my surgery.My problem so far is no appitite.I just have no desire to eat,and the only reason i do eat is because I know i'm supposed to.I believe when I go for my appt.I will be put on long term meds.I hope this will help with my appitite.

wesley1
Joined Oct 19, 2012

Thu, October 18, 2012 3:01 PM

I suggest you read the books

Protein Power

Eades, Michael R. (Book - 1996)

The Protein Power Lifeplan

Eades, Michael R. (Book - 2000)

If you use the eating plan , take Metamusil daily.

Talk to your Dr about your plans before beginning.

mrx
Joined Apr 20, 2012

Wed, October 17, 2012 10:45 PM

Reply posted for KyleB125.

I used to do all the recipe books for crohns, no spicy food, cooked veggies, no skin on veggies no grease ect. Once talking with my Dr he said if my crohns wants to flare it will regardless what I do and don't eat, so now I eat basically what I want. Even though I have constant pain there are times I feel worse when eating certain things after multiple experiences with the same food, as in severe stabbing pain and running to the bathroom hours after eating. Foods that are naturally harder to process such as ice cream, creamy sauces, spicy food and potato skins seem to effect me even worse than it would someone not diagnosed. Which sucks cause I love those foods, so I limit myself and will maybe have ice cream when I know I'll be home for the weekend, everyone is different but starting to write what you ate when you have a flare may help if you start to see if certain foods relate to your symptoms and can help you decide to eat them agin or not.

blonde157
Joined Oct 17, 2012

Related Topics

Weight and Eating

KelseyShoup
Joined Sep 26, 2020

Hello so I've been struggling to get my weight....

read more

Nausea and Vomiting with ...

crystal73d
Joined Aug 4, 2021

Hi all- I have been diagnose with Crohns disease ....

read more

Help losing weight

Twinsnana
Joined Feb 13, 2022

You're definitely not alone. I have Ulcerative....

read more

Welcome to the Crohn's & Colitis Community!

This website is associated with the Crohn's & Colitis Foundation.

Please read our Top 12 Rules before posting messages and sharing stories. Always be courteous and sensitive to others!

Intended audience. The Crohn's & Colitis Foundation Online Community is intended for patients and their caregivers, family and friends. The Community is not intended for industry representatives or advertisers and these individuals are not permitted to participate on the site.

Meet the Crohn's & Colitis Community! Browse our site to see what our community is talking about and find issues important to you.

Join in and share your stories. After you feel comfortable with our site, register to share your thoughts on a regular basis.

Stay secure. Remember that our site can be viewed by anyone on the Internet. With the exception of our registration and personal pages, search engines are available within this site. To guard your privacy, follow these simple rules: do not share your address, phone number, details about your family, or anything else you would feel uncomfortable with others reading. If you post your personal email, be aware that you may receive spam e-mail from spammers who gather addresses off of the web.

Read and react to posts with care. If you don’t agree or are offended by someone’s post, take a step back and think before you reply. Since we can’t talk in-person to each other, we must recognize that we may be misunderstanding stories or posts. Please be sensitive to others’ feelings and ask for clarification before acting out.

Search before starting new topics. To keep our message boards easy to use, please use the search bar to locate topics of interest before starting a new thread. If you start a new thread, please use obvious subject headings and words that will catch the attention of others. Topics will be archived after 21 days of inactivity. To view past topics and posts, click on archive topics within each of the forums.

Stick to our guidelines. To keep this site safe for everyone, please do not post: doctors' names, treatment facility names and treatment specifics, contact information for others without their consent, links to websites with uncertain content or advertisements, requests for fundraising, items for sale, requests for study, survey and/or questionnaire participation or provocative information.

Sharing photos. Please use good taste and appropriate images when adding photos to your profile or personal stories. Photos should be in .jpg format.

Not following the rules? Crohn's & Colitis Community moderators routinely scan the message boards and will delete tasteless posts. If you post inappropriate messages or pictures or use offensive language in a post on multiple occasions, you will be notified via email and your account will be inactivated.

Report foul play. Help the Crohn's & Colitis Community moderators by reporting anyone that posts inappropriate messages or pictures by clicking the 'Report Abuse' button under the message or emailing ccfacommunity@ccfa.org.

Questions or concerns? Please feel free to email us at ccfacommunity@ccfa.org with any questions or concerns. We want you to feel comfortable here.

Terms & Conditions. By posting your story, questions, concerns and other information on the Community, you grant the Crohn's & Colitis Foundation or its authorized agent permission to publish, reproduce, record and use your stories as Crohn's & Colitis Community or the authorized agent sees fit in any medium or forum in a manner which helps to further the Crohn's & Colitis Community mission. You agree to release and hold harmless Crohn's & Colitis Community from any and all liability by any third party that may arise from the release of information to any third party or by any third party and agree that all text and other content made by you, for you or the person for whom you are the parent/guardian, shall be the exclusive property of Crohn's & Colitis Community. The Crohn's & Colitis Community cannot verify every claim made by a third party contributor to our Community and is not responsible for the authenticity of information posted.

Thank you! The Crohn's & Colitis Community is successful because of members like you!

Thanks!
The Crohn's & Colitis Community Team

*Any postings on the Crohn's & Colitis Community site should not replace your physician's advice. Always check with your personal physician before taking any action regarding your health.