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.

complications from UC/Crohns

Wed, March 04, 2009 1:00 AM

Hello everyone,

I've had UC for 11 years now.I'm waiting on my colonoscopy as soon as my cardio sends my medical clearance to my GI.I'm suppose to be on lialda once daily. but I stopped it (bad I know) because of how I've been feeling. I started taking it on sunday. and about 1am monday morning I started getting excrutiating abdominal pain, to the point where It felt like i could catch my breath. it went on for the whole day, untill i went in to see my gastro. the pain eventually went away,but now theres this tenderness on the right upper side of my abdomen and I cant walk straight up,i'm slouched alittle. I have to go in for a ultrasound tomorrow,because my doctor thinks it might be my gall bladder. mind you, I 've had these pains before in the past while on colozal,and it never ended like this.this is really scary for me. has anyone ever had any complications from UC or Crohns? what could this be? thank you.

Dawn

dawn28789
Joined Mar 4, 2009

Thu, March 05, 2009 1:00 AM

Reply posted for ACA11.

thank you so much. I went for my ultrasound this morning. the GI will get the results within 48 hours. I do feel a little better. when i walk it hurts a little,i'll have to stop and rest. but it's still not as severe as it was yesterday. my GI also had put me on a bland diet...he didn't say how long. but I'm continuing it untill i feel 100% or as long as I can tolerate it. believe me, I need the fluids anyway.

dawn28789
Joined Mar 4, 2009

Thu, March 05, 2009 1:00 AM

Reply posted for dawn28789.

It very well could be gall bladder. My first GI doctor (if you want to call him that) found gallstones in me April 2007 and it took them until October 2008 to take my gallbladder out. It made a difference. But now, I really have to watch what I eat because of the liver now producing all the bile without the help of the gall bladder.

Since my surgery, I can no longer eat red meats and a host of other things. People tell me that eventually I will, yet these folks don't have Crohn's either.

I hope your visit will answer some more questions for you and you will soon be pain-free. We're rooting for you!!!!

aca11
Joined Mar 3, 2009

Related Topics

IBD and trauma

Janeliza
Joined Apr 13, 2022

Hi all! I've had Crohn's since 2014 with m....

read more

Life Insurance?

Aperson1
Joined Dec 2, 2022

40 y.o. male looking to get life insurance. ....

read more

IBD and exercise/sport

JS25
Joined Aug 14, 2023

This is my first post. I am 28 and I was diagnosed....

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.