My two year old daughter has cf and doesn't take anything by mouth. Her cf clinic had to switch enzymes to creon when she was on pancreacarb. It wasn't a problem before,since we were able to put it down her gastronomy button, but this creon is not supposed to be put in there. We did try it and it clogged. We were told by her doctor that the only choice was to make her take it by mouth, but we can't get her to swallow it. She cries and makes her self sick with it still in her mouth. The FDA won't approve the pancreacarb that worked with her g tube. Any suggestion?