u/LandscapeOk6338

Long story short after NSAIDs I got chronic gastritis and esophagitis(no helicobacteria). Unbelievable nausea and vomiting then I started ppi feel fine after 3-4 months but after 1 year( I am on ppi 2 years now) I feel nauseous whatever I eat or not. Morning nausea, eat smt nausea do not eat nausea, motion sickness (I didn’t have my first +20years of life but it started after ppi mostly). Can’t stop ppi bc gastritis also causes nausea.And I can’t get test for sibo because I am still on ppi
So I am thinking getting some antidepressants after speaking my gastroenterologist

Özet geçeyim tedavi için kullandığım ağrı kesiciler sonrası özofajit ve gastrit oldum ama yok böyle bulantı ve kusma(anksiyete,yanma vb de var). Bilimsel yöntemler yabancı kaynaklar cart curt hepsine baktım uyguladım ama 2 yıldır sorun yaşıyorum bir de üstüne mide koruyucu kullandığım için ibs semptomları yaşıyorum. Yok bu şöyle ben bunu şunu yaptım iyileştim diyen? Babaanne yöntemleri olur, ilaç olur fark etmez.

Okay gastritis is suck. If someone say their finger in pain because of gastritis I believe them. Anyways I feel like my whole body is always in pain. Like 3-4/10. Ik about low vitamins minerals and I use supplements for that. I feel like I did some exercise and my body in pain but nope.
So I saw ppi can affect mitochondrial activity too? May be that’s why I feel more tired now than when I first diagnosed gastritis even my symptoms were worse in the beginning.
But my stomach and esophagus are so sensitive they have hyper active cells(that’s why some people feel symptoms and some doesn’t) i want to stop taking them but also scaring about symptoms