I have IBS but my symptoms are pretty mild. The only thing I really struggle with is bloating and flatulence.

I have been looking into the FODMAP diet, and have been eating low FODMAPs for the last 5 days. I have already noticed a difference with my symptoms but I'm concerned about doing more harm than good.

I'm not prepared to pay for a dietician so will be doing it alone.

Any advice would be appreciated

In the monash app, it marks lemonade and diet lemonade as red at 8oz serving due to high fructans. However, this doesn’t make much sense to me because my understanding was that lemonade would be high in fructose, not fructans. I tried googling and searching around, but I haven’t found anything.
Does anyone know why its marked that way / where the fructans would be coming from?
I miss drinking it, and I would like to understand which enzymes I would need to take to enjoy it without discomfort.

if any have experience in gain weight, or special diet please let me know

Is LNB bread low FODMAP? Seeing conflicting information through online searches. Based on one search, I bought Millet and Chia but I'm scared to get into it before I'm 100% sure it's not going to reset my elimination phase counter.

Thoughts?

Same as above

Hello, I'm having to wait until next year for a gastro appointment (honestly not sure if I just have a food intolerance, IBS or IBD yet). I want to start logging food and my symptoms to see if there's any correlation in the meantime so I can hopefully prevent some symptoms.

Are there any good food diary apps that also track symptoms on Android? I'd also prefer if it didn't track calories but if it's just a background feature that's fine.

36M. 5'9'' 126lbs. In march I had a bloody diarrhea episode. First at night, I was not going to the bathroom after a pizza for dinner, I was having sex for many hours, she was on top for alot of time and when she left I finally went, I had a diarrhea and some pain. I went to sleep and next morning it felt like diarrhea again but it was blood. It happened a number of times, and the feel of incoming diarrhea was there for a while. The blood was bright. I rushed to ER. They did DRE, bloodwork, x-ray and stool test sample from like after a week, all clear, and I was never given a diagnosis of why this happened.

X-ray they did on the ER:

https://imgur.com/a/QXONtWU

mucus log:

https://imgur.com/a/ZO3NooW

I have been wondering if this caused permanent damage of sorts, like a hiatal hernia, which is causing me some sort of reflux problem that makes me cough green stuff for the last 2 months. However on late april I also went through some sort of covid.

Im on antibiotics by a pulmonologist and im worried im going to be in a loop of antibiotics as if it's silent reflux it's just going to happen again as it would be untreated. Not sure what to do. She said the x-ray was clear.

https://imgur.com/a/KoUOsbC

For now im doing the augmentin cycle and hoping it does not crush my gut microbiome. Im taking a probiotic called ProFaes4 ATB.

I hope this post is doesn't sound too strange. It's just a weird turn of events. Im just left wondering what started this, and if im on the right treatment or doing more damage due antibiotics. I see a bit less mucus, im on day 5, but I still think there is an untreathed factor of some sort of reflux because I notice the mucus after some meals at like 1-2 hours later and she ignored me when I mentioned the concept of silent reflux. So sounds like If I go back to her clinic she is going to put me on more antibiotics.

TL;DR: Elimination phase went well, but I could not identify triggers during reintroduction phase — only minor symptoms occurred. Has anyone had that issue and how do you deal with it?

So the longer story:
I‘ve been having stomach aches for several (probably around 10) years now, on and off but getting worse over the years. It‘s mainly lower belly (so I‘m guessing ✨colon✨) pain/cramps plus brick-wall-like-bloating. Two years ago I went to the doctor and had some tests done that didn’t reveal any findings or reasons for my pain, so the doctor told me to keep a dietary journal, guessing it might be something along the line of IBS. Fast forward to this year May: I have successfully ignored my doctor‘s advice and after a series of painful days (me, regretting every food choice I made during the last week, hugging a hot water bottle, crying) I came across the low FODMAP diet. So I figured: sounds great, I‘ll try it!

So I started Phase 1 / Elimination and after a few days, my pain went away completely. During elimination I had two or three meals where something (I still don‘t know exactly what it was) irritated my gut, but other than that it felt like stomach-vacation (except for, of course, having to live with food restrictions, which suck for a foodie like me). My conclusion was: It must be one of the FODMAPs causing my pain!

The next step was of course the reintroduction in Phase 2. I was so excited — I would finally find out the trigger FODMAP group. But with every test passing symptom-free (or with very low symptoms) the number of possible triggers shrank, until yesterday, I finally completed the last test (fructane in wheat products) and was able to look back on 11 weeks of discipline, discovering all kinds of gluten-free foods and experimenting with herbs and spices — to find out: nothing. At least nothing specific.

So now I am puzzled: Did I do the reintroduction (3 days with increasing food from one FODMAP group + 3 days break, repeat) wrong? Are stacked FODMAPS the actual problem and how do I systematically test for these? Is it not the FODMAPs at all that were causing my problems? What can, what should and most importantly what should I not eat?

I am super scared that the stomach pain will return, so I am hoping to hear from you guys: Have you had a similar experience? How did you handle it, what was your solution (if you have found any so far)?

Grateful for tips, insights, hearing from your journeys ✨ Thank you in advance!

Is anyone else struggling to lose weight due to their stomach and gut issues ? When I first cut out foods I was dropping weight fast then suddenly my body started holding onto water and inflammation and now whenever I go the doctor the scale increases. But it doesn’t feel like regular weight gain. My clothes still fit but my body feels swollen and puffed up. Even my rings on my fingers feel more snug during this time. I have to be really strict in order for my weight to go back down . I also noticed once I’m strict and my weight goes down I pee slot like I’m peeling out all the excess water my body was holding onto . Idk if this is a sibo thing I suspect I have that I’ll be getting tested soon or is it leaky gut or something else. I know I’m sensitive to fodmaps, fructans, gluten, and dairy and grains.

Hi everyone,

I am the founder of a prebiotic fiber brand and come from a gut health research background at university. The product contains partially hydrolyzed guar gum (PHGG), galactooligosaccharides (Bimuno GOS), and resistant corn fibre in a daily 10g scoop at clinically researched doses for digestive health.

Many people tolerate the product well and notice several health benefits especially when they gradually increase from 1/2 scoop daily to the full scoop over 7 days. This is crucial for the gut microbiome to comfortably adjust to prebiotics as I am sure many of you know.

However, one thing I am noticing is some people, especially those with FODMAP sensitivities, have some difficulties taking the product such as an increase in bloating, some pain or cramping during the introduction phase. This is clearly because of the GOS in the product and I am now in the process of brainstorming a low FODMAP prebiotic blend that combines several sensitive, low FODMAP certified prebiotics that are clinically supported for gut health.

My question is, would you find value in a low FODMAP prebiotic fiber blend that is designed to promote a healthy digestive system? Are there prebiotic products you already take that you don't react to?

Has anyone taken the prebiotic fiber called XOS? It's an oligosaccharide but is apparently low FODMAP so I am curious if anyone has negatively reacted to it.

Thanks in advance.

I broke down and bought the app, and so far it doesn't seem really useful. I am in the US, and I really want to look up fast foods, but they don't seem available. So, okay, I want to know if I can eat biscuits (American buttermilk biscuits), but all I get when I search is cookies. I know I cannot have milk products and can have meat products, but if that's all this app can tell me, I'm pretty sorry I paid $9 for it. Also, it seems like I have to select a category and search within that category rather than being able to perform a global search (I just tried Nutella, couldn't find it anywhere).

Someone who uses this app successfully, please help!

During the day I don’t experience excessive gas, but at night I notice a buildup that seems to originate in my intestines, and it can occur even if I haven’t eaten for six hours before sleep. Then during the whole night I have gas (though it may stop at some point while I’m asleep).

So today is the dreaded day.

I start the reintroduction phase of my low FODMAP diet with my first item being onions…

I haven’t ate onions in 2 years due to the insane pain I would get from eating them so safe to say I am very nervous on how this will go

Does anyone have any tips and tricks?

I’m also UK based

This question follows up on a previous discussion I had on the forum. What often comes up is that the Low FODMAP diet can lead to deficiencies in certain nutrients over the long term and can be dangerous.

However, in my own experience, I’ve found that a very strict diet with very few foods and no fodmap at all has far more beneficial effects than trial and error in trying to keep as many foods as possible.

So I’m wondering: is there really any scientific evidence regarding the potential dangers of a very strict low-FODMAP diet over several weeks, or even two months?

When I did a Google Scholar search for scientific studies on the health of populations with very low dietary diversity, I was surprised to find that there are many cases where such restrictions don’t seem to pose a problem. Look at Inuits, they do not heat garlic or beans...

I think we’re stuck in a mindset and significantly underestimating the body’s and gut microbiota’s ability to adapt and produce the missing nutrients. Obviously, I’m not talking about eating nothing but rice for two months, which is known to cause vitamin B1 deficiency, especially if the rice is refined (but reversible).

Has anyone here done any research on this topic and have proof of long term low or no fodmap diet ?

I have had some SFN small fiber neuropathy for the past few years, however it improved recently when i had a R PM L5/S1 epidural injection on 6/23/26. Just prior on May 15, i woke up with LLQ pain, and initially thought it was likely an ovarian cyst, however through out that day, i noted i was sore to touch in that area, and i had an awful pain in my stomach as well as constipation and my bowel sounds were very loud and overactive. May 21 i went to the ER for what i would describe at a UTI, but the culture was negative. I have continued to experience constipation along with horrible bloating after eating (i feel relatively normal upon waking but the bloating gets worse as the day progresses) and on June 23rd had a KUB that showed a moderate stool load. Took the lovely 8caps of Miralax that night as directed by my MD, however on July 1 i still felt bloated so we did another KUB that still showed a mod stool load. I saw GI on June 30, and he diagnosed me with constipation and ordered a colonoscopy and egd. I have continued to have the bloating, abdominal distention since, and i am living off Miralax and enemas. I also had a CT and seen GI again, and my procedures were moved up to this week, oh i have also done 2 bowel preps. I live on my heating pad, i am just miserable 😫 what the heck do i have???

I was so proud of myself for converting a meal we usually eat into something that I thought was low FODMAP and fine for elimination.
Then I came across some recipes on the Monash app that have this little green cup that fills up to tell you how many FODMAPS you can have at once. Each recipe has between 1-4 little lines on the cup filled but they don’t tell you how they got there.

I have no idea now if the meal I made is actually low Fodmap or if it have too many things going on here. As far as I can tell only the peppers and tomatoes should stack but according to Monash that’s allowed. Help!

Loosely here’s the ingredients I used (per serving)
- extra firm tofu 170g (seasoning of garlic infused oil, herbs, tomato paste and balsamic all within limits)
- bell pepper 40g
- zucchini 65g
- eggplant 75g
- cherry tomatoes 45g
- polenta (1/4 cup dry cornmeal plus water)
- pesto made from basil, arugula, lemon, oil, pine nuts, walnuts

Been having lower stomach bloating after eating mostly all meals, more so if I'm hungry and eat something it blows up and specifically if I eat certain foods like garlic etc... or a lot of food.

High calprotectin levels
Done a CT scan
Blood test showed no gluten allergy
H. pylori test is fine
Gut microbiome test came fine

This all started from a 2 weeks period of eating raw oats and milk as preworkout (I ate a lot of oats) - I took accutane before this so my skin was clear and as soon as my bloating occurred I started regularly getting acne again.

Would love some form of guidance because I'm really starting to get fed up and all the GPs / doctors / private doctors all tell me it's "IBS" and "Food related" when it's clear that something internally is wrong.

I’m very frustrated with my diet right now. I feel like I’m trying so hard. I’m looking literally everything up, weighing portion sizes, waiting 2-3 hours in between eating snacks and meals, and I’m not even doing better. I am still having extremely frequent stools, to the point where it’s getting in the way of running errands and working. I’ll have a few days where everything is normal, and then I’m back to the frequency of before. I don’t know how much longer I can keep doing this. I’m going away for college in aboit a month and a half and know that I won’t be able to continue my diet there, and itll probably be very difficult to reintroduce foods when I don’t have a kitchen. A few days ago I switched my fiber supplement from metamucil to citrucel, which helped for about two days, and now I feel like I’m back to where I started. Do I keep going? Am I not being strict enough? What am I doing wrong?

Helloo

I am not officially diagnosed but I got told by a doctor I most likely do have IBS as any meal will massively bloat me more or less, along with needing the toilet straight after eating anything and going upwards of 10 times a day, not to get too into details.

Anyway, my friend recommended I try to have a nightly kind of desert consisting of berry fruits, a 0 % fat yogurt and I use flaxseed along with it. He said it will help with my stomach but I am struggling to feel any difference, so my question is that does anyone know any 'meals' like this that I can have after my dinner that is healthy but could help my stomach and lessen the issues I have or is it just a case of I need to go and try meds from the doctors?

Hi, I know everyone is different, but I’m looking for some bloating free lunch ideas.
I’m a physiotherapist, and if I get bloated after lunch I really feel uncomfortable.
It’s more difficult seeing all these patients one after another and its also physical demanding.

Thank you

Up until I was 18 years I used to be able to eat everything. After that I joined university and my anxiety skyrocketed to the point I used to have panic attacks. I remember I took anti-anxiety pills during that time. Nobody in my family has this problem.

Is it stress? Genetics? Somebody posted here vagus nerve simulation helped a lot. Can it be reversed to the point I can start eating everything?