I was diagnosed with GP a year ago. Slowly got better with diet adjustments. About 3 weeks ago all symptoms hit at the same time along with the feeling of shortness of breath, chest pain and heat skipping beats. I went to the cardiologist who ran all the correct tests including wearing a heart monitor for 24 hours. It showed I am having large number of PVC's when I eat/drink anything. Said that the heart is fine and to go see the GI Dr.. He believes the heart is being affected by the vagus nerve. I can't see the GI Dr. until next week so I have tried to reduce intact to liquids and is some better.
Has anyone else with gastroparesis experienced PVC's in relationship with your eating/drinking? I can't find any resources on the Internet about the two?