I have had 4
ERCP's...the
firstFirst progesterone mc10
First progesterone mc5
First-progesterone vgs 100
First-progesterone vgs 200
First-progesterone vgs 25
First-progesterone vgs 400
First-progesterone vgs 50
First-testosterone
First-testosterone mc was because of intense right upper quadrant pain, vomiting, nausea, diarrhea, etc. and the doctors could find nothing else wrong so they did an
ERCP with manometry. The manometry showed a number of 50. They
cutCuts and puncture wounds the
sphincterAnal sphincter anatomy
Inflatable artificial sphincter of the pancreas. I still was having problems, so they did another
ERCP with manometry and this time the number was 200...so they cut again and they gave me pancreatitis. I spent 9 days in the hosptital. A couple of years later, I was told I needed another ERCP..this time they put in a shunt..which they removed a couple of days later. About a year later, another ERCP. I am still in pain, still have chronic nausea, chronic vomiting (it is not too bad as long as I don't eat normal food)and chronic diarrhea. I was diagnosed with gastroparesis, had polio as a child and now apparently have Post-Polio syndrome and I have degenerative disc disease in my low back and neck. I was just sent to a gastroenterologist by my new primary doctor to see what "new" stuff is available. He ordered an MRCP which showed no biliary tree problems..but the blood tests show ALK Phos at 179 (normal is 40-120) and ALT at 65 (normal is 9-52). This guy wants another ERCP...BUT I DON'T!! He already told me that I have to stay on a "liquid" diet because of the gastroparesis...so why bother when the ERCP will cause me SEVERE pain and SEVERE nausea, etc. I would like another opinion...are the liver tests that out of whack considering my other problems?