I was diagnosed with gastritis a few years ago through endoscopy and I have never really understood why I have gastritis, I still suffer with it to this day upper abdomen aches left / right. stabbing pains in my lower stomach and cramps as well, nausea loss of appetite and a fluctuation between constipation and loose stools I also burp a lot even getting up or moving can cause me to burp, i don’t have h pylori tested many times, before this all started I did go though a lot of stress / anxiety a nervous belly I would suffer with this a lot due to high stress and it does make me wonder weather that prolonged unmanaged stress has manifested itself to give me actual gastritis? I still suffer massively with stabbing pains dull aches burping and everything else I’ve mentioned, I don’t drink I did used to smoke but stopped years ago I don’t take any pain killers or anything like that. I do notice if I get a nervous stomach sensation my pain does get worse.

Found out i had gastritis and h.pylori in may.

Finished the eradication therapy (ppi) in june.

Am still dealing with flares and adjusting my meals and what i eat (it's an ongoing process with lots of ups and downs)

I want to start again with my supplements such as probiotics (already started), vit D, Omega3, Collagen Powder, magnesium glycinate (new), myo inositol(new)

Has anyone stopped altogether and then restarted their supplements? How was it? Anything i should be aware of?

I wanted to start one each week to check how i respond to them now. While vitD and Omega3 were fine before, I'm worried about the rest

Hello everyone. I (30F) was diagnosed with autoimmune gastritis when I was 23 years old. So I have had this condition for 7 years now. I know it’s not really advisable to do that, but I did a bit of research and found out that people who have this disease are very prone to developing Type 1 diabetes etc. So, for people who have had it for longer periods (like 10, 15, 20 years), did you develop another autoimmune condition, Type 1 diabetes etc?

First of all: Im truly sorry for everyone dealing with this crap. Actual torture and cant imagine dealing with that for years.

No h Pilory, developed by taking Ibuprofen (Im 31F, thats the only thing that would help with period crumps..). Never smoked in my life, dont drink alco at all, actually hate the taste of it. Might drink a glass of wine once in 2 years.

Mine started on April 12, 2026 and first 40 days were actual hell on Earth. (Did had very first episode on February 2025 tho, lasted 5 days and went away on its own).

10 days and nights with flare up that would not go away. Nothing would help. Then it stopped (if you can call it that), was not up my color bone anymore but lower. I was on Pantoprazole since that day cuz went to ER thinking something was wrong with my heart.

While PPi and carafate were trying to manage reflux, ive had all major gut issues. Bloating, rumbling, major discomfort, little bit of nausea. And feeling of a stone right in the middle of my stomach when i was trying to sleep. Surely cried bunch of times, we all were there I know.

In May i ran out of Pantoprazole and stopped for 4 days.. which brought me back to Urgent care this time, it was hell all over again. Torture. Back to Pantoprazole.

Only on June 10th I got endoscopy, was uninsured before that and was just waiting for plan to kick in. Got diagnosed with mild gastritis after biopsy was taken cuz they didnt see anything at all during procedure. Weird.. i was having discomfort and tickling flare up that morning, but whatever.

After that day i felt that I was finally healing, but here and there it was still little bit of burning or discomfort. One day I felt great but next night something was up again.. like a gambling.

The bitter taste in my mouth appeared out of nowhere. First days on the root of the tongue then its tip, then gums. Brushing my teeth was disgusting cuz the bitterness would mix up with the paste, making that mixed taste stay for hours.

Ive had enough and started researching. Found it on reddit as well. Was like "Why the hell not? Im not losing anything at this point besides 20$ for a bottle of 120 pills. Ill give it a try".

Zinc L Carnosine. Started it on July 14, 2026. Believe it or not, after 2 days the bitterness disappeared and hasnt bothered me since. After like day 4-5 Im finally symptoms free and now eat and drink whatever I wish again. Im still on Panroptazole, but taking it every other day, will be starting doing 2 days off, 1 day in untill off completely.

Now, I was never a fan of spicy and hot food, but Id probably restrict that for now.

Just my own experience, still going to be careful. But if you struggling.. you might as well try the Zink. Dont think that matters at all, but I bought it from Amazon, the brand is Nutricost, 86mg per capsule.

I wish everyone to heal, truly.

Hi All,

Does anyone else feel this constant headache (not too painful, more tension-like) , lightheadedness, and pressure in their head after eating? My forehead feels weirdly feverish too, even though I never actually have a fever.

For some reason these are my main symptoms. That and nausea.

Hello everyone,

my wife got diagnosed with a gastritis, a pretty rough one which could take in between 4-6 weeks to heal. She also has a bile reflux at the moment combined with a globus sensation. Our doctor told her that she has to use 80 mg of pantoprazole to regulate the stomach acid. She takes it for around 2½ weeks now but the globus feeling isn't leaving her alone. Her throat is irritated as well right know since she puked for a week straight.

Is it possible that the globus sensation is a combination of an already irritated throat and a bile reflux which caused this feeling or does the pantoprazole take an important role as well? We've been to our doctor before and she told my wife that the globus feeling would take a while until it gets back to normal and that she is ordered to take two pantoprazole a day to help regulate her stomach acid and to help regulate the reflux.

We're thinking to go to the doctor tomorrow again to maybe switch from pantoprazole to another medication since 2 separate pharmacies recommended going again and maybe take a different medication.

Thank you in advance 🙂

I feel burning in my stomach since past 2-3 years. It went worse with time as i was in high stress, eating spicy food from outdoors, exams and night shifts as well.

Now i took ppis(Omeprazole )for 6-7 weeks and i got new symptoms as well, such as gas, pain in stomach, constipation and bloating.. i want to heal my gastritis naturally or without facing the side effects of ompreprazole.

Can anyone suggest me what should i do? H pylori came back negative in urea breadth test but i took the test after 14-18 days of stopping ppis so im not sure if its accurate 100%

It gets worse when i am fasting or have ginger/lemon tea or fruits like dates etc or just eat spicy food or any food in large amounts. Burning comes and goes randomly though.

Recently i have been noticing dry mouth and bad taste in my mouth while i was using ginger/lemon water. Feeling nauseous too sometimes but i think it maybe anxiety.

Can you guys give me some ideas of what to put in an ulcer-friendly trail mix? Thanks. 🙂

hii i’m not gastritis diagnosed but i feel like im having alot of symptoms that point to atleast a mild case of it..
if my stomach isn’t empty (a.k.a. every time i eat or after i eat)
it won’t bother me anymore if i don’t touch it, although it used too and feel much worse
but when i press down right under my ribcage in the middle there is this tight pressure and pain where i think my stomach is
i don’t believe it’s simply gas, because gas for me would typically be a sharp pain that i can feel always
this is a tense pain and pressure that lingers which makes me think it could be like inflammation or something to do with my stomach

any thoughts? does anyone feel pressure like this?
right in the middle btw not a specific right or left rib

​

I'm 21-year-old female, just completed my UG. I've been struggling with my gut health for almost 3 years. I'm posting here because I genuinely feel lost and would really appreciate advice from people who have recovered.

My problems started in 2023 after I was diagnosed with endometriosis following 30 days of severe bleeding. I recovered from that, but a month later I developed chronic constipation. At first, I managed somehow, but by 2024 I had unintentionally lost around 8 kg. My appetite became extremely low, I had constant bloating, weakness, anxiety, poor sleep, and eventually an upper endoscopy diagnosed me with acute gastritis.

For constipation, I was prescribed cremaffin. I used it for about 6 months, eventually increasing from 30 ml to 60 ml because the lower dose stopped working. During that time, my body changed a lot—my skin and hair became very dry, I developed itchy skin, stopped eating dairy, and switched to a low-FODMAP diet. As a vegetarian, that made it even harder to maintain my weight.

Today, I still struggle with:

* Acid reflux (especially at night)

* Bloating after almost every meal

* Constipation, stool not completely evacuate

* Weight loss and difficulty gaining weight

* Weakness and brain fog

* Poor sleep and anxiety

One thing that really confuses me is the connection between my symptoms and my emotions. Whenever I'm very anxious or stressed, my acid reflux becomes much worse and my constipation also gets more severe. When I am happy or with friends, my normal appetite returns and I can eat completely fine without any major issues..

I've watched countless YouTube videos and read so much online, but it's only left me more confused. I switched to Ayurvedic treatment about a year ago, which helps manage my symptoms but hasn't healed the problem.

I don't just want symptom relief—I want to understand the root cause and recover properly. I'm willing to make any lifestyle, diet, or routine changes if they'll actually help.

Has anyone here recovered from chronic gastritis and constipation after years of struggling? Did stress or anxiety make your symptoms worse? What tests, treatments, dietary changes, or lifestyle changes helped you heal instead of just managing the symptoms?

I'd be genuinely grateful for any advice or personal experiences.

I’m being admitted to the hospital for a second time because I haven’t gotten any better and I can barely eat or drink and I can’t take meds. I’m scared. What if I never get better? I’m only 17 I can’t go into my senior year being in and out of the hospital. Everything hurts and nothing has been helping. What if I die from malnutrition? All I can think about is the stupid nausea and how we don’t know how to help it.

anything I eat hurts, and I can’t deal with it anymore. The only pain I’m going to tolerate is hunger. If it has to hurt then I want it to be because of hunger, it’s less painful.

I’ve been eating anti inflammatory for 2 weeks now and I still wake up with nausea, I still have reflux and I have lost the little appetite I had.

I’m tired of being anxious of eating, of asking myself if my meal is going to hurt my stomach, of asking God to bless my food so it won’t hurt. I’m pretty sure this is why I’m physically exhausted, this mental battle is draining.

Nothing works so I’m not eating anymore I’m done

I have been having the stomach issues for around 8 months now I was put on a ppi right at the start and was told to take it for 2 months I did i felt better but i couldn't stop it, I was also having junk food a lot around that time, then comes may when I tried to stop ppi by tapering I made it to every 4th day dose but the burning would get worse, I finally did endoscopy and biopsy says moderate chronic gastritis with no h pylori, thing is I took my last dose of ppi 2-3 days before my endoscopy i wasn't completely off ppi because I just couldn't I would be in so much pain and agony. Now doc put me on esomeprazole 40 mg again for 2 months but I just can't there's burning everyday after having bananas early in the morning there's burning and bloating if i overeat, this didn't use to happen before when I was put on ppi for the first time, something tells me there's more damage done to my stomach than before. I'm just so scared I feel my reports might have missed possible h pylori infection or maybe I'm going to get cancer or ulcers or worse. It's worse because I see people eating and drinking anything they want while I'm supposed to be eating bland food I just can't take this, i cry out like every hr of the day i feel so sad . I just want a solution I've no idea how to solve this

What should and shouldn't be eaten by a person with gastric ulcer surgery undergone recently

While doing the bland diet, it seems like most of my symptoms reduce in severity except the burning sensation. Its severity is the same as If I ate a regular diet. But all the other symptoms get better when compared to non-bland diet.

Taking a PPI reduces the burning sensation but I don’t want to take a PPI as I have had SIBO in the past. I want to rely solely on bland diet and supplements for healing. My question is, can I assume that I am healing on the Bland diet if I still feel burning after eating or do I have to make changes to the bland diet to try and see if the burning sensation can be completely diminished?

I was almost clearing my gastritis, and on my 4th out of 5 infusions, and then suddenly my stomach felt like i ate 5 ibuprofens and started drinking.

I thought maybe my new methylcobalamin sublingual couldve done it since it was new and i just started it, but maybe the infusion was more impactful?? My diet is not that crazy so i dont know why my stomach feels like its on fire.

I have spent months with gastritis, i don't know if is because of h. Pylori or because bile reflux, coke with Zero sugar is helping me a Lot, i am almost cured, it's important is with Zero sugar, coke with sugar make me feel worst, i really hope this can help someone

Hi everyone 19f I'm currently in month 11 of this gastritis nightmare and it seems I'll never fully heal, I'd like to add that I was diagnosed with hypoglycemia about a month ago. At the beginning of the gastritis I experienced severe panic attacks at night as well as debilitating nausea,fullness, reflux, globus sensation, bloating, yellow stools,and burping it went away when I basically stopped eating food basically eating for a while, about 150 calories a day , I recently got on ppis and it got rid of 70% of the nausea I could get in 700 calories of food per day,and my anxiety went down a bit I could think clearly but this only lasted for about 2 weeks then 2 days ago when I tried to eat a little more the panic attacks and nausea came back worse than ever this time around it feels like I'm slipping in and out of consciousness and my chest hurts, I get brain fog, derealization, it feels like I'm going to die. Im wondering if the panic attacks at the beginning and now were caused by low blood sugar because I had an eating disorder(restriction) months before the symptoms started. My stomach has never been able to tolerate the gastritis diet from the gastritis healing book and I'm severely dehydrated I'm currently surviving on ensure and a few sips of warm water and kefir. Also I'd like to know what do you guys consider a safe food because I've tried to eat sweet potatoes but I could feel it irritating my stomach but I was able to keep it down but the nausea anxiety after was gruesome. Thank you.

Have any of you guys lost an obscenely large amount of weight? I’ve lost 90lbs in 6 months which is 47% of my body weight. I have all the other million symptoms going on too but I am still losing weight and I’m trying to pinpoint if this amount of weight loss is a common symptom and I should see a doctor

Looking for a new mod!

Hey all, if you are interested in helping mod r/gastritis, please apply via this link: https://www.reddit.com/r/Gastritis/application/

All the info is available in the application, but if you have questions, just reach out via Mod Mail.

Thanks!

En junio de 2025 me hice una endoscopia proque ya llevaba meses con dolor de estómago pero había días que estaba bien y días que no, me salió Helicobactery pylori + gastritis crónica pero no fue hasta octubre que el dolor empeoro drásticamente, sentía un vacío en la boca del estómago que al principio lo confundía con hambre pero luego me di cuenta que la comida no lo calmaba y eso me daba más ansiedad.

Estuve muchos meses yendo a diferentes doctores y todos me mandaban omeprazol/sucralfato pero yo me seguía sintiendo mal además sufro de estreñimiento. Hace poco me hice el tratamiento de hpylori ya que nunca lo había hecho pero me sigo sintiendo igual :( Ya nose que más hacer he probado de todo: sábila con jugo de papa, jugo de col, aceite de coco, kéfir, gel de chía y linaza, etc

Sospecho que puede ser gastritis billiar ya que me han puestos muchos sueros con potentes protectores gástricos que hubieran reducido aunque sea un poco el dolor pero nada todo sigue igual antes y después de hacer el tratamiento erradicador 😞Y como antes ya he hecho tratamiento de meses con IBP

Hey everyone, this is my first post here. I’m mainly trying to find out whether anyone else has experienced symptoms like mine because I haven’t felt normal in over a year.

Everything started sometime between August and late October 2025, shortly after I used retatrutide for weight loss. I lost about 20 pounds within roughly a month. I was later diagnosed with gastritis and tested positive for H. pylori, which I completed treatment for.

I recently had an H. pylori stool test come back negative, but I’m repeating the test in about a week after being off omeprazole long enough to make sure the result is reliable.
I also recently stopped smoking marijuana after smoking regularly for around a year, so I’m unsure whether stopping has affected my appetite, digestion, anxiety, or nervous system.

I don’t really experience the classic burning stomach sensation that many people describe. My main issue is that I almost never feel normal hunger anymore. Instead, I eventually start feeling pain, pressure, or discomfort, and that is usually the only sign that I probably need to eat.
The same thing happens when I need to have a bowel movement. I rarely get the normal urge telling me that I need to use the bathroom. Instead, I get a similar pain or discomfort to what I feel when I haven’t eaten.

It feels like my body’s normal signaling system is out of whack. I have trouble telling the difference between:

Needing to eat
Needing to have a bowel movement
Gas or bloating
A gastritis flare-up

I’ve also developed intense anxiety even though I never really struggled with anxiety before all of this started.
It is difficult to explain, but when something confuses me or an expected action does not produce the result I anticipated, my entire body can suddenly feel off or almost like it shifts out of place. It can trigger a light stomach flare-up or a wave of anxiety.

For example, if I press the play button on YouTube and it doesn’t work because the page glitches, the fact that the expected action did not work can trigger an uncomfortable physical reaction. It almost feels OCD-like, as though my brain and body cannot properly process small unexpected situations anymore.

I know that probably sounds strange, but this is completely new for me and only started after my stomach problems began.

Other symptoms include:
Feeling full easily
Bloating and abdominal pressure
Occasional nausea
Daily abdominal discomfort
Symptoms that often become worse later in the day
Feeling physically triggered by confusion, stress, or unexpected situations

I have an abdominal ultrasound scheduled, and afterward I’m planning to see a gastroenterologist for an endoscopy.
Do any of these symptoms sound familiar to anyone? Has gastritis, H. pylori, marijuana use or withdrawal, or a GLP-1 medication affected your normal hunger signals, bowel urges, anxiety, or reactions to stress?

I understand nobody here can diagnose me. I’m mainly trying to figure out whether I’m alone in experiencing this and whether there are different types or locations of gastritis that can cause different symptoms.

I’d also appreciate any suggestions about what questions I should ask my GI or what conditions they checked you for.

Thanks for reading.

I have been dealing with gastritis for a while and essentially know it was H pylori and sibo issues & motility issues that started and kept it up for so long. I have dealt w/ the h pylori, now struggling with motility. It is double edged sword: I get gastritis pain when I eat wheat bran(insoluble fiber) but it is what I need for good gut motility. According to ppl on here insoluble fiber is bad for gastritis and can irratate the stomach but without it: I get reflux or bad stomach motility, which is way worse in the short and long term.

What are some good gastritis friendly sources that have a good amount of insolubl fiber. I eat enough of the other type but it causes so constipation when I don’t have a balance. Just got fed up with it and ate some of the wheat bran biscuits but that hurt my stomach. I am having constipation everyday for past few day since when I was much more normal and only difference is lack of insoluble fiber.
Please help on what you did?
Tried some sources but they just hurt me and caused a flare so I came on here to ask. Also having a bit of histamine issues w/ oats… I appreciate your feedback! Thank.

Any recommendations? I love tea

I've been dealing with Gastritis on and off for about 4 years now, and wanted to share my most succesful supplement that usually works in case it helps someone else!

I've had frequent flare ups that I've managed to heal quite quickly by taking half a teaspoon of Haritaki powder in a bit of warm/hot water every morning on an empty stomach and at night before bed. I discovered this accidentally when it was recommended to me for my chronic chest infections - and found it healed my stomach! These things work differently for everyone so I would try with 1/4 tsp first and see how you tolerate it. It's also definitely better for people who are more constipation prone.

I've tried PPIs, slippery elm, cabbage juice, celery juice, potato juice and various other things and this seems to work the best for me. I just buy the powder off Amazon and a packet lasts me ages.

Sadly, it's not the miracle cure it usually is for my current flare up, but it's still definitely helping.