I am a caucasian female, 5ft. 5 in. tall.
When I turned 18yrs. old. I noticed severe stomach distention (I looked 5-6 months along), after I consumed what I considered a 'normal' lunch. A whole wheat deli sandwich, w/ some potato chips, and maybe a pudding.
I went to digestive doctors. They stated that I was severely lactose - intollerant and that I was wheat - gluten sensitive. So, I've stayed away from milk/dairy products and by ezekiel bread.
I still had stomach pain. So, I went to the Mayo Clinic. They diagnosed me with gastroparesis. So, I learned about nutrition. Tried various digestive pills, reglan and many others. I ate 4 - 5 times a day. Eight years goes by with me just 'dealing' with chronic pain.
This year, 2009, I re-visited my local digestive doctor. He told me to go to Kansas University, in Kansas City, KS. I went. Ate the eggs with the radioactive thing added. Took x-rays for 4 hours. This test indicated I had 'Dumping Syndrome'.
I am hypoglycemic. So, I suck on a jolly rancher or two w/ my meals throughout the day. I avoid liquids an hour before and an hour after my meals. I eat 3-4 times a day. My vagus nerve is severely damaged. My pyrlorus muscle doesn't open and close properly. It sorta just sits there.
Here is my question:
Sometimes after I eat. It could be 20 min. - 3 hours after, I will 'pass out' from immense pain. My breathing gets very shallow. I sweat or sometimes my arms get cold. I may 'pass out' from 45 min. - 2 hours.
The only drug that has touched my chronic stomach pain has been liquid morphine. I had it several years ago in a hospital setting, because I had passed out from my stomach pain.
I go see a new doctor in Austin, Tx. this coming Sunday (Feb. 8)
Does anyone else have a life like mine? All doctors seem to be able to tell me is that they don't know. I know I have digestion issues. Its the chronic stomach pain I am trying to find a solution to.