Hello! This group was created for the purpose of bringing all those together that have pancreatitis due to Cystic Fibrosis. In my years of researching the internet for information about my particular type of cf, I have yet to talk to someone that has the same symptoms as I do. I have been told by my physician that I am considered the minority of the minority and there probably will not be any clinical trials for my type of disease. The reasoning given for this was that people are not dying from my type. So it seems the search never ends for answers to this thing. Anyone and everyone is welcome to join this group.