gastroparesis and help treatment
I'm getting tested for gastroparesis, I had a test in 2018 but was never told I was borderline on my stomach not emptying. I've had stomach problems a long time , GERD, reflux, bloating, can't eat much and my constant cough. Some digestive problems can cause chronic cough. So it's the "rule out this game" now. Next stop my pulmonologist.
Have a great day and any information is welcomed
Interested in more discussions like this? Go to the Digestive Health Support Group.
What are your symptoms? I was diagnosed over 15 years ago. I have problems with nausea, vomiting, and I can go for days without eating. It’s one of the major signs of neuropathy.
I started losing alot of weight and nausea and vomiting 🤢 24/7. I have severe malabsorption and malnutrition. I do also have 2 types of neuropathy. I have been on a feeding tube and pump fed into my intestines for the last ten year's. I have many gastric problems and chronic pancreatitis. They all seem to be getting worse every year. I have bile reflux that has damaged my esophagus and I have barrett's esophagus. Now I also have Olgivie Syndrome that temporarily paralyzes my colon,intestines and bowels. They are trying medication but I am still struggling badly.
I have this cough at. Night so it has to do with digestive problems which I have.
Diagnosed after ten years on tramadol. Given reglan which helps but is not a long term med. Calmed my symptoms down. I take intermittently when I have flares. Also on a low fiber diet.