Irritable Bowel Syndrome (IBS)

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Irritable Bowel Syndrome (IBS)
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Hello there! 👋

We're so glad you're here. Scroll down to find some of the Crohn's conversations happening in our community. The more, the merrier—jump in anytime!

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10 reasons to join the Crohn’s and Colitis Support Group

1. It’s full of other people with connections to IBD.
2. It’s a safe forum to ask any and all IBD questions.
3. It’s a way to connect with others on the Mighty community.
4. I’m one of the group leaders (living with #UlcerativeColitis ), and I’m pretty cool.
5. We want to normalize talking about poop.
6. We do Q&As with partners like Girls with Guts.
7. It’s a small but “Mighty” community that we want to grow.
8. It’s supportive.
9. Why not?
10. Do it today!

You can search the groups to join. #CrohnsDisease #InflammatoryBowelDiseaseIBD #ChronicIllness #IrritableBowelSyndromeIBS

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The Mighty's Crohn's Disease community is 76,000+ people strong, but there's always room for more. Follow along or join in today—whatever is comfortable for you!
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What is something you wish people knew about living with Crohn's?

What is something you wish people knew about living with Crohn's?

Your response may be used in an article or video on The Mighty.

#CrohnsDisease #ChronicIllness

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Where To Start #ChronicIllness #Undiagnosed

2020... I had an IUD taken out thinking my severe sharp cramps were because of the IUD. Doctor put me on estrogen birth control and my menstrual cycle took a turn for the worst. I had a plague of symptoms that all were so severe. From severe lower back pain(I could not sleep on my back, had to sleep on my side, I couldn't just roll over, it hurt to even sit on the toilet. When I drove I had to sit on a circle pillows to keep my tailbome off the seat) I also had heavy peirods(clots, severe cramps then went into my inner thighs and would hurt my already painful back, light spotting carried on after peirods and in between periods, it was as if I only had a week off of bleeding a month) I had the worse bum cramps, peeing hurt all the time(burning, having to urinate often) Sometimes if I didn't pee I'd get sharp pains. Id have either constipation, diarrhea sometimes, depressive episodes. I couldn't wear a tampon(I ALWAYS wore them with no problem) but suddenly they didn't sit up there anymore, they'd get lodged sideways and fall out. I was forced to wear large pads. I couldn't physically go anywhere. It was a big deal to leave the house. Anyways fast forward. 2021-2022 I found a lady doctor who put me on Visanne, said if it worked it is likely Endometriosis. It worked. 98% symptoms gone. But I began getting severe left sided pain(and lower abdomen pain) She told me I needed the diagnostic surgery. Met the gyno. Specialist (who doubted it was Endo, thinks its IBS which I'm not against but that doesn't answer my menstrual issues) she put me on Myfembree. Which worked like gold! Fast forward again(after arguing with a gynecologist, I thought, "I just want to make sure it is endo and if we can get ahead of it") I had my surgery last week, they didn't find anything. She said it was just painful periods. (Btw, she BARELY read any of my history the lady doctor wrote down for me over the years, this specialist didn't read barely anything.) She isn't looking into my issues anymore. She said we will do a six week follow up on your surgery incisions and that's it. It sits so wrong with me. The medication is working, but I discussed with her before the surgery that the last med stopped working and I'm concerned about that happening again and she agreed. But now it's not a concern? I'll probably go visit the woman doctor again but I feel like I'm being ridiculous now. I feel like I'm overboard or I shouldn't be worried. Is there not other conditions this could be? Because I looked up the confusing word(painful periods) and that does not tick off my symptoms. Anyways, that's my very shortened story. Sorry about that.

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I'm new here!

Hi, my name is iamsickandtired1994. I'm worried about getting a laparoscopy? Doctors want to check for endometriosis…after 10 plus years of IBS and ICPBS symptoms. Has anyone done this procedure? It it worth it?

#MightyTogether #IrritableBowelSyndromeIBS #InterstitialCystitis #ChronicFatigueSyndrome #Endometriosis #PTSD

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Grateful

I just want to take time to say how thankful I am to make it to 37 weeks pregnant! Due to having EDS, I was expecting to have a preterm baby(as I have in the past) but my little girl has made it to “term” and looks like she might make it to full term! I can't wait till she is here and in my arms.

In terms of my chronic illness its been a rough ride (though a textbook healthy pregnancy ) but its almost over and the joy of being a mamma again is about to begin. Thankful to God and all my loves ones who have supported me through it all!!!

#EhlersDanlosSociety #EhlersDanlosSyndrome #EDS #ChronicPain #ChronicFatigue #IrritableBowelSyndromeIBS #Asthma #migrains #EosinophilicEsophagitis

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CHRONIC C

I SUFFER FROM IBS CONSTIPATION 3 AND ITS A BLOODY NIGHTMARE ANYONE FEEL ME, ABUSE ABUSE OF EVERY LAXITIVE ECT. FORNLASTC3 YEARS,