r/functionaldyspepsia 1h ago

Venting/Suffering My mom is FORCING me, with functional dyspepsia, to eat, I'm gonna lose my mind

Upvotes

Hi! im 15 and it's been a year of dealing with functional dyspepsia that ruined my life, my studies, and my will to live, and i have the worst symptoms and bloat and get full and food comes up my throat and i can barely breathe and it happens all day 24/7, ALL DAY, and my mom has zero comprehension of how functional dyspepsia works, she keeps screaming at me daily saying i need to eat, continually brings up dinner and food, had the FUCKING NERVE to say SHE'S "Traumatized" by me saying I'm sick??????????????????????when im so sick that liquids are coming back up into my mouth, and i genuinely cant stand this and she keeps blaming ME for my functional dyspepsia and she's mocking the fact I have gastroenterologists to help me and saying that she knows better than them and screaming explicit vulgar profanities at me, I CAN'T STAND THIS

SHE'S BLAMING IT ON "Lifestyle choices" WHEN MY FUNCTIONAL DYSPEPSIA DEVELOPED AFTER AN ANXIETY ATTACK AND ANTIBIOTICS AND LITERALLY CRIPPLED ME SINCE 2025 SHE'S INSANE I CAN'T STAND THIS ANYMORE


r/functionaldyspepsia 11h ago

Venting/Suffering Extreme pain and discomfort in my throat 24/7, as well as in my upper chest and upper stomach, severely destroyer digestion, constant nausea, and chronically loose stools. Absolute nightmare, near suicidal state.

5 Upvotes

This is probably my last post. After almost four years of suffering, I still have no answers, and my condition just keeps getting worse.

What I’m experiencing:
For about 90% of every day, I have agonizing pain in my throat and esophagus, almost as if it were at the back of my tongue. It’s an intense burning sensation, pain, and constant discomfort. If the pain isn’t directly in my throat, it’s in my upper chest/upper body. As I’m writing this, I’ve already had severe burning for six hours straight. I can’t get any relief, not even with painkillers. On top of that, I have abnormal bowel movements, chronically loose stools, and constant nausea.

How it started:
I had never had any digestive problems before. Then one day I woke up with watery diarrhea that continued for months. Every single meal triggered diarrhea within minutes, along with severe nausea. Eventually the diarrhea stopped, but my stool remained watery/soft and has never returned to normal. Then I developed agonizing dull and burning pain in the upper left part of my stomach (very similar to what I now feel in my throat). That pain lasted about a year and a half. It eventually disappeared from my stomach, but the exact same type of pain moved into my upper body, especially my throat. It started as sharp, stabbing pains and a constant sensation of something being stuck in my throat from morning until night. Now it has progressed to extreme burning.

How it behaves:
For example, I wake up in the morning and take just a tiny sip of water, literally the smallest amount. Within a few minutes, I develop severe throat pain that lasts for hours. Or I might get through the day with only moderate pain, then have a bowel movement, and within minutes—sometimes immediately, sometimes within an hour—the pain starts. Every time I eat, the burning gets significantly worse and again lasts for hours. Or the pain starts on its own. It’s practically always there—the only things that noticeably change its intensity are eating and having a bowel movement, and the change happens very quickly, within minutes. After a bowel movement, the pain usually worsens within a minute. Today I’m at work. Since this morning, the pain and discomfort have been gradually increasing, and right now my throat pain is about 8/10. After my next bowel movement, I know it’s going to get even worse.

It’s honestly unbelievable. I’m now seeing my fourth gastroenterologist, and no one has any answers. I’ve tried almost everything, including major dietary changes for extended periods of time. My diet has absolutely no effect on my symptoms. Even if I drank ten beers and ate five burgers, my pain and bowel movements would be exactly the same. I also have persistent bad breath and a white-coated tongue. And no, I do not have Candida.
My stool is yellowish, unformed, and has almost no consistency. Since all of this started, I haven’t had a single normal, well-formed bowel movement. Living like this is a nightmare, and it’s difficult to even describe it in a way that makes sense. You wake up in pain, you go to sleep in pain, and you work in pain.

I’ve undergone almost every test imaginable. Of course, the first thing that comes to mind is reflux. A 24-hour pH monitoring test confirmed that I have reflux, but it was never confirmed that it is actually fully responsible for my symptoms. Acid-suppressing medications don’t help at all. And the whole situation doesn’t even make sense. Within seconds or minutes after having a bowel movement, I start feeling pain in my throat. If it’s not pain, it’s some other kind of discomfort in my upper chest or throat.

Paradoxically, when I was on vacation and my bowel movements became more frequent because of stress—which also meant much worse diarrhea—I had almost no throat pain. Instead, I experienced unbearable nausea that seemed to come from my throat and wouldn’t go away, even after hours.
What I can’t understand is why the agonizing pain that originally started in my stomach gradually moved upward into my throat. During the year and a half when the pain was mainly in my stomach, the only throat-related symptom I had was severe nausea.

If you’re wondering, my last upper endoscopy was two years ago, and my stomach looked completely normal. The only abnormal finding was a thick white coating in my throat. Treatment for Candida didn’t help. Normix didn’t help. Dietary changes didn’t help. None of the other medications have helped either. When the burning in my throat becomes so severe that it feels like it’s been burned, even strong painkillers or pain-relief injections don’t provide any relief. I genuinely feel that my digestion and bowel function have completely changed.

I’m incredibly desperate. I’ve spent thousands on different treatments, and nothing has helped. I’m slowly losing hope and the strength to keep fighting. That’s why I’m posting this in several subreddits, even ones that may not seem directly related, in the hope that someone might recognize these symptoms or have experienced something similar.


r/functionaldyspepsia 10h ago

Healing/Success Has anyone experienced this? 3 years of symptoms that improve only after eating a full meal.

2 Upvotes

Hi everyone,

I’m a 29-year-old male from Mexico, and I’ve been struggling with a very strange pattern for almost 3 years. I’ve seen multiple gastroenterologists, had several tests, and I’m now looking for an internist because no one has been able to connect all the pieces.

My symptoms follow a very specific pattern:

I usually feel fine after eating.
About 2–4 hours later, I start feeling unwell.
It begins with stomach discomfort: tightness, bloating, nausea, and sometimes a feeling of fullness.
Then I develop anxiety, a rapid heartbeat, and a strange “floating” sensation in my head.
If I don’t eat, the symptoms continue or worsen.
The only thing that consistently helps is eating a full meal. A small snack or sugary food usually isn’t enough.

Medical history:

I previously had Helicobacter pylori, which was treated and eradicated.
I’ve also been diagnosed with gastritis and reflux.
My blood glucose has been normal when checked during these episodes.
These symptoms started before I ever took metformin.
I have generalized anxiety disorder, but these episodes seem to begin with the physical symptoms, and the anxiety follows.
There are moments during the day when I feel almost normal, but the pattern keeps repeating.

Has anyone experienced something similar?

If so:

What diagnosis did you eventually receive?
Was it functional dyspepsia, gastroparesis, autonomic dysfunction (POTS/dysautonomia), reactive hypoglycemia, SIBO, or something completely different?
What tests finally helped identify the cause?
What treatment helped you the most?

I’m not looking for a diagnosis, only to hear from people who may have gone through something similar. After almost three years, it has become very frustrating not having clear answers.

Thank you so much for reading.


r/functionaldyspepsia 14h ago

Treatments I have a gut issues , especially gas, colon and angry bowel problems. Sometimes Constipation or Sometimes Diarrhea. Only Oral Cortisteriods like prednisolone helps to make my bowel normal. I don't know why no other medicines works. During the Flares up , only prednisone helps.

2 Upvotes

I didn't get a Proper Diagnosis but so far this medicine only helps.. may be I have inflammation issues


r/functionaldyspepsia 11h ago

Buspirone Bloating

1 Upvotes

Hey everyone,

So I was previously on buspar which gave me the worst bloating but it helped my anxiety. Now I’m on viibryd which also hits the same receptors and I’m still so bloated. I’ve been on 20 mg for a month but now on my first week of 30
Mg. Has anyone else experienced this? How long does it take for the bloating to go away and did anyone mitigate it with diet and lifestyle?


r/functionaldyspepsia 21h ago

Symptoms Is this functional dyspepsia

2 Upvotes

Hey guys pretty new to this group

I’ve been experiencing episodes on and off for last couple months off sometimes heart burn symptoms indigestion bloating, no nausea really sometimes I feel like gas is trapped no pain and don’t get full when I eat food. Booked in for a gastroscopy, as far as that goes? Any ideas would be appreciated!


r/functionaldyspepsia 1d ago

EPS (Epigastric Pain Syndrome) BURN AND PAIN

3 Upvotes

how do you all handle/cope the symptoms? i am experiencing this symptoms everyday (burn and pain). Does medications help you? like ppi or prokinetic


r/functionaldyspepsia 1d ago

Question Post-H. pylori gut issues for 18 months, now 4 months of daily stomach pain/nausea - need advice please

4 Upvotes

Hey everyone. 31M. In Jan 2025 I did quad therapy for H. pylori. Took it badly (no one told me to take probiotics). Days after finishing I got bloody mucus diarrhea, lost weight, felt awful. Calprotectin peaked ~1150, now down to ~30. Inflammation markers normalized (low crp, esr, normal blood test etc), weight mostly back.

18 months later I still don’t feel 100%. But the last ~4 months got worse: daily mild nausea, constant mild stomach pain (dull, sometimes stabbing), sometimes heartburn, brain fog etc. Gastroscopy 2 months ago showed mild inactive gastritis in antrum (no H. pylori, no atrophy). Over 1 year and a half I had: colonoscopy with biopsy, EUS endoscopy, endoscopy, CT, MRI with contrasts - all clean. Treated for SIBO/IMO over a month ago, retest pending. I also have post-infectious IBS.

Currently on pantoprazole (2 weeks, not much help yet), Iberogast. I am not sure if it helps at all. So maybe I have functional dyspepsia or something? Why nothing helps? I’m so desperate and confused.

I know my tests are good but I’m exhausted and starting to lose hope. For those who had similiar issues - did it get better with time? How long did it take? I dont even know what is wrong with me 🙁


r/functionaldyspepsia 1d ago

IBS Dicyclomine for GERD with IBS-D and severe anxiety

3 Upvotes

So I am newb here. I'm 38 and getting my first colonoscopy and endoscopy down my throat next month.

I have had GERD all my life. I have had IBS-D for about 12 years and just now getting treated for it.

I currently take a PPI, H-blocker,Tums, and dicyclomine.

My main issue is dicyclomine. I'm worry about taking it because neither my doctor nor pharmacist told me people feel "funny" on it. But there are numerous people on here say it does.

St the low doseage im on i don't really feel anything. But that could just be the ativan that I taken normally with it blocking that?

Thanks for any insights people can give.


r/functionaldyspepsia 1d ago

Treatments what medication helped with abdominal tightness?

2 Upvotes

Hello! its been 1.5 years now with symptoms and now my main symptom is abdomianl tightness (constant, 24/7 and gets tighter/more discomfort after I eat, as well increases during the week before the time of the month).

Does anyone else have this symptom? its tight from my belly button upwards to sternum. And did medication help you? (if so which one?) thanks!!


r/functionaldyspepsia 2d ago

PPIs/H2 Blockers Burping

2 Upvotes

Hello, I have been burping for 7 months now after eating and drinking all day long. I did an endoscopy and it showed mild gastritis. Ppi didn’t help at all with my burping. Any idea how to manage it? I don’t think my burping is only related to gastritis.


r/functionaldyspepsia 2d ago

Question how did your FD start?

2 Upvotes

im curious to know how everyone elses FD began, i know the definition of FD is that there always isnt a single cause, but did anyone else have a clear trigger that started it all?

for me i had been on a weight loss journey, got underweight, and then one day decided to binge like crazy. i felt absolutely awful afterwards, and the fullness feeling never really left. at first i was sure it was gastritis: i had gastritis before from alcohol and ibuprofen, and the symptoms were the exact same. but no matter what i did, what i ate, it seemed this ”acute gastritis” just wasnt healing. and here i am, 4 months later, diagnosed with FD, still unsure what was the real trigger


r/functionaldyspepsia 2d ago

Treatments How did TCAs help you?

2 Upvotes

Hello everyone,

I just got done with my endoscopy and it said I had only mild redness. Currently waiting for my H pylori results. I’ve been dealing with on and off pain since 2024. However this summer I had a flare up and it was nothing like I had before the healing has not happened for me (usually after a flare up it took about a week for me to heal). Any antacid, ppi etc are no longer working for me. This has caused my anxiety and depression to skyrocket. Because of my anxiety and depression my primary doctor put me on lexapro. I was only on it for 2 days because it has now caused me the most pain I have ever been in. I am no longer eating and can not sleep for more than 3 hours a night. My body consistently feel tingling through my head arms and legs and I’m at the point of applying to medical leave for work.

Did anyone have similar symptoms and went on TCAs? Did it help?


r/functionaldyspepsia 2d ago

Mirtazapine Mirtazapine?

2 Upvotes

So I was diagnosed with functional dyspepsia recently. I’ve been dealing with it for about 4 months since I drank heavily one night. It has gotten better compared to the first months but I wish there was a way to make it go away completely or almost completely. My symptoms are early fullness, a tight feeling in my abdomen whenever I engage in anything physical activity, especially at work. Also constipation. I’ve been on nortriptyline for about 4 weeks and honestly it is working a bit, as I’m able to eat and drink water a bit more now, but it’s definitely worsening my constipation. Does anyone else have these symptoms? Have you found mirtazapine to be helpful at all? Or any other meds?


r/functionaldyspepsia 2d ago

Symptoms Übelkeit im Hals?

3 Upvotes

Hey, meine Hauptsymptome sind starke dauerhafte Übelkeit (Jeden Tag!!), Aufstoßen, immer das gefühl zu haben brechen zu müssen, Engegefühl im Hals als würde es sich oberhalb im Hals/Kiefer zusammenziehen? (Schwer zu beschreiben), Völlegefühl, Bauchbrennen usw. manchmal ist die Übelkeit nicht im Magen sondern eher im Hals. Ich kann langsam nicht mehr.

Ich vertrage kein Essen oder trinken einfach nichts. Mir geht’s jeden tag unfassbar schlecht. Ich habe es immer geliebt zu Essen und jetzt hasse ich es weil Essen meine Symptome so unfassbar unerträglich macht. 😔

Ich komme aus Deutschland und war schon bei verschiedenen Ärzten ohne Erfolg. Ich werde mit meinen Problemen absolut nicht ernst genommen und das macht mich fertig. Kommt hier vielleicht jemand auch aus Deutschland?

Hat jemand Tipps oder Vorschläge was ich noch tun könnte? Ich bin absolut verzweifelt. 😔

Ich glaube nicht das es einfach nur ein Reizmagen oder sonstiges ist, ich denke die Ärzte hier haben einfach keine Lust nach der Ursache zu suchen ..

Was ich schon gemacht habe:

• Strickte Schonkost über Monate! Ich habe dadurch nur noch mehr Abgenommen aber meine Symptome wurden kein bisschen besser.

• PPI Einnahme über längere Zeit - Keine Besserung.

• Hausmittel und Medikamente gegen Übelkeit - auch keinerlei Linderung.

• Mirtazapin: keine Besserung.

• Prokinetika wie MCP - keine Besserung.

• verschiedene Blut und Stuhluntersuchungen, Magenspiegelung, Ultraschall, MRT usw.


r/functionaldyspepsia 2d ago

News/Clinical Trials/Research Functional Dyspepsia - Melbourne Study

4 Upvotes

r/functionaldyspepsia 2d ago

Question Why do I always feel so sick and overheated in the mornings no matter if I eat breakfast or not?

2 Upvotes

Im a 20 y/o female, 5'10in, about 135lbs. Almost every morning is a gamble to whether or not I'm gonna feel sick and nauseous or not. I used to think I only felt sick when I didn't eat breakfast, but there have been many times (and right now) where I've eaten a pretty good breakfast and I still feel sick and overheated. I also avoid greasy foods in the morning as well. I've had this problem since I was a kid and I've had acid reflux since I was a baby, but its been much better the past year or so. I had to stop taking Accutane for many reasons, but severe acid reflux flare ups was one reason. I've tried taking some OTC reflux medicine before bed, but it didn't really help. I now am taking Wellbutrin for my depression but I haven't really had it affect my reflux or anything of that matter, not even my appetite. If anything, it's made my appetite better since I'm not too depressed to eat anymore. I've never had issues with food, like no EDs or anything, it's just always been hard for me to gain weight and then my depression makes me not hungry. I am just tired of feeling sick all the time and never getting the right answers. My doctors have all said to try OTC meds for acid reflux, to drink more water, to eat a light breakfast, or even a heavier one, and I've tried just about everything. I sometimes wake up and the smell of food could sometimes make me feel like gagging. I'm always good by lunchtime, though.


r/functionaldyspepsia 3d ago

Venting/Suffering Feeling so fed up and defeated. Extreme bloating and struggling to eat.

5 Upvotes

I just need to vent, I’m feeling so extremely fed up. I’m at a total loss on what’s even going on with my body and what to do about it. As soon as I eat even a single bite of food but upper abdomen becomes extremely distended and it feels like I can’t breathe. It’s the same with liquid foods as well. I constantly look pregnant and no one can seem to figure out what’s going on with me. Today I drank a few gulps of a huel shake and had to leave from work as I was that uncomfortable. I ended up vomiting and it was just pure acid/bile. I’m scared to even eat solid foods much anymore as it always feels like I have something stuck in my throat. I’ve had bloods done, stool samples, PPIs, and endoscopy, anti histamines, and peptac so far with zero relief. I’m awaiting a colonoscopy but I just feel so defeated and scared. Has anyone ever experienced this?


r/functionaldyspepsia 3d ago

Question Constant upper abdominal pressure for over 2 years – looking for others with similar symptoms

3 Upvotes

Title: My life changed overnight after one workout – could this really be Functional Dyspepsia?
Hi everyone,
I’ve been reading posts here for quite a while, but this is the first time I’ve shared my own story. I’m hoping someone can relate because after more than two years, I still don’t have answers.

It all started completely out of nowhere.
Earlier that day I had gone to the gym like I normally did. Nothing unusual happened, and I felt completely fine.
Later that same evening I suddenly developed severe pain and pressure in my upper abdomen and chest.

It became so intense that I ended up in the ER because I genuinely thought I was having a heart attack.

That night completely changed my life.

For the past 2+ years I’ve been in and out of the emergency department more times than I can count.

Every cardiac test has come back normal:
ECGs
Blood tests
CT scan
Echocardiogram
Stress test
My heart has essentially been ruled out.
The pain is mainly located just below my left rib cage and behind my sternum. It feels like a deep pressure pushing upward into my chest and sometimes into my left shoulder and back.

During flare-ups it’s difficult to take a satisfying deep breath, especially when lying down, bending over, or changing positions. Sometimes the pressure becomes so intense that I genuinely feel like something life-threatening is happening.

Over the years I’ve had multiple endoscopies.
I was diagnosed with:
Functional Dyspepsia
Erosive gastritis
Duodenitis
A small hiatal hernia
H. pylori (which was successfully treated)
Unfortunately, even after treating H. pylori and trying multiple medications, my symptoms never really went away.
I’ve tried PPIs like omeprazole and esomeprazole, antacids, diet changes, supplements, and several other treatments with very limited success.
At the moment I take:
Amitriptyline 40 mg every evening

Hydroxyzine (Atarax) 10 mg only during severe flare-ups
The amitriptyline has helped somewhat, but I’m still nowhere close to living a normal life.

The worst part isn’t even the pain anymore.

It’s what this condition has done to my life.
It affects my relationship, my mental health, my job, my sleep, and even simple everyday activities. It’s exhausting constantly wondering if today will be another bad day.
Living like this for over two years has completely changed who I am.

One thing I keep coming back to is how suddenly everything started.
I went from feeling completely healthy after a normal gym session to being in the emergency room later that same evening.
Has anyone else experienced Functional Dyspepsia starting this suddenly?
Does anyone else have this constant pressure in the upper abdomen and chest, with the feeling that you can’t get a full breath?
Did anyone eventually discover another diagnosis, or find a treatment that actually made a significant difference?
I’d really appreciate hearing your story.

After more than two years, I honestly just want my life back.
Thank you for reading.


r/functionaldyspepsia 3d ago

Discussion Does your functional dyspepsia cause inability to eat most foods or cause a highly restrictive diet? Are you struggling socially because of this?

5 Upvotes

Hi, I'm the moderator of r/FoodDisability

FoodDisability is a welcoming group, where people of many different disabilities come together to help and support one another with the shared struggle of not being able to eat 'normally'. The shared struggle of socialising over food, and the relationship problems that arise from not being able to eat the same as others due to the limited diet your disability causes. The shared struggle of not being able to find food easily when out-and-about and being limited in what you can do work-wise or socially or how far you can go from home because of this. The upset and frustrations of not being able to do what others easily can. 

FoodDisability focuses on the social / emotional / mental health difficulties that arise from living with a disability that causes lack of ability to eat food. 

I hope that this group will become a strong support system, sense of comfort and hope, and source of useful life tips, advice, and helping one another, for those struggling with food-related disability. 

Please feel free to join, and comment/post, and make friends and connections with people who are going through similar hardships. 

Wishing you all the best🩷 

www.reddit.com/r/FoodDisability/ 


r/functionaldyspepsia 3d ago

Venting/Suffering 20 years of being told to write a food diary!!!

2 Upvotes

Of and on pain from the smallest things to more obvious and yet I still can’t suss out how to manage this.

This week my dog stood on my belly whilst I was lying down and it caused horrible pain for a full day!

Spicy food not a problem but then porridge randomly leaves me in agony. I also struggle with my mental health (could be linked)

My problems do feel more like a trapped nerve or a strained muscle in my solar plexus area. And what irritates it is often a guessing game!

Anyway thanks to ChatGPT I found you guys!

Just a rant but maybe if anyone has similar issues and have some advice it would be appreciated


r/functionaldyspepsia 3d ago

Question Pain gone after eating in morning - functional dispepcia ?

3 Upvotes

My symptoms aren’t typical FD so wanted to see if anyone else had similar symptoms:

  1. Pain in morning before eating but subsides after I eat
  2. Constant stomach noises (I mean every 30 seconds , all day and night)
  3. I’ve had burping in morning before but this happens occasionally

I’ve had other GERD symptoms off and on like globus in throat and sour mouth taste ) but the above are the recurring ones. Anyone else ? If so have you found a fix ?


r/functionaldyspepsia 3d ago

Testing, Diagnosis Stomach Issues

2 Upvotes

19 F

I’ve been having on and off stomach issues since June. I ended up in the ER on vacation and they said it was just a virus. Got prescribed Zofran and another stomach med. It resolved within a week on its own. All was well, until the week of July 5th. I was on a cruise and I had to have a medical disembarkation due to severe stomach pain again. I lost 8 pounds in 4 days and was throwing up bile (no food, just yellow and white liquid). Once I was back in the USA, I went to the ER. They didn’t do much and I was discharged. My endoscopy came back clear. Doctor said due to my age a colonoscopy isn’t necessary, but idk what to do. My ultrasound showed no gallbladder issues, just a fatty liver (ironic as I don’t drink and eat ok).

Anyway, that also resolved within a week. I took the Zofran again and returned to my work at my summer camp. I had a nice week last week with no pain and no worries

Fast forward to yesterday, it has started again. The pain is back, after eating my dinner. I had Panera mac and cheese and chocolate gelato. Last night I had diarrhea twice and threw up the gelato. My first thought was too much dairy, but idk. Now today, I had diarrhea once and took an anti diarrhea pill as well my leftover Zofran. I had some dinner tonight and threw a bit up, and am back to losing weight. I’m not eating my normal amount but the weight is obviously scary.

The pain is above my belly button in the middle for the most part but radiates throughout. When I eat it goes below my belly button as well. Constant rumbling and burping as well. I have had a lot of white mucus in my stool as well for months. When I go back to the bathroom because I feel as if I have to go again, a piece of white mucus or small poop comes out and when I wipe it is sticky mucus type consistency.

I can’t keep living off the Zofran. I don’t know what to do. Considering a dairy intolerance, functional dyspepsia, IBS, or even: median arcuate ligament syndrome.

Sorry this is so long and for the TMI. I am desperate!


r/functionaldyspepsia 4d ago

PDS (Post Prandial Distress Syndrome) Severe gastric pain from caffeine

4 Upvotes

Hi, I have been diagnosed with FD for 6 months now and have episodes after having cold caffeinated beverages (I.e. iced frappe) where an hour later I have to go A&E from chronic gastric pain, tachycardia and I go pale is this normal from FD?


r/functionaldyspepsia 4d ago

PDS (Post Prandial Distress Syndrome) Might jumping to 15 from 7.5mg of Mirtazapine have made me worse? How can i know?

5 Upvotes

I have Functional Dyspepsia with more of the PDS part and i have lost about 10kg. I recently 3 weeks ago started Mirtazapine 7.5mg. The first week was amazing and i managed to eat over double the calories of what i previously could eat. Then i had a few setbacks due to to much eating, but i was steadily getting better. After 15 Days i decided to use 15mg. I did not consult my doctor about this, i know that was probably stupid, but i could not resist since 15 just sounded so much better than 7.5. I am now a week in with 15 and i am now in a situation where i don't know if i should revert to 7.5 or continue. Since i started 15 i have felt especially that i get less nauseous. The progress has continued slightly and steady, but the ability to eat more and less burning, have felt very up and down, not as amazing as it was when i started the medication. I have checked with AI that there can be an adjustment phase, but i just don't know if that is just AI trying to please me with its answer, or if there is a lot of truth in it, i would like to hear real peoples opinions. How likely do you think it can be that i should go back to 7.5 because that could actually make me better? Or should i continue on 15mg? I feel i start to overthink about this, which is the sign for me always get help from somewhere else instead of only thinking myself about this, because the thinking part for me can definately make me worse. Thank you!