Hello!
I am completely new here, and I will admit, completely lost and a bit hopeless.
I was diagnosed with IBS about 18 years ago. It was sort of managable. I get more diarrhea then constipation. I have a couple of food intolerances like dairy, eggs, caffeine, garlic as well as ceoliac’s disease.
Things started getting worse in 2015 after I got my gallbladder removed. I have terrible acid reflux(I take Pantoprazole twice a day) as well as slow digestion(I take Domperidone twice a day.
Since 2015 things have gotten worse every year. For almost two years now I’ve had chronic nausea coming from my oesophagus. It got really bad this summer as I lost all appetite and was unable to eat.
I’m being followed by a gastroenterologist and a nutritionist. Now I’m able to eat about a meal and a half a day, the rest of the time I take Boost for supplements.
I have been unable to work or go to school since July. The doctors don’t know what’s wrong. I took tests as well as colonoscopies and endoscopies, but no real results, only that there is inflammation in my blood.
Is it commun for IBS to have such strong flare ups? And is there something to do?
Thank you for reading.