Every doctor who wanted to perform it would have to file an IND application and get the FDA’s approval.

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Their homebrew killed off the superbug, and Catherine founded The Fecal Transplant Foundation to educate other C.

diff patients about the simplest and cheapest of all remedies: poop. diff survivors and looked forward to learning how her new foundation could help connect patients with transplant providers.

As she browsed the registration sheet, she found her first surprise.

Out of 150 participants in this public workshop, she was the only member of the public. Catherine felt out of place — and intimidated again.

“And at one point I was in renal failure.” After a friend found her unconscious in her house, she was rushed to the emergency room and spent three days in the hospital.

These severe dehydration incidents left a permanent mark — Catherine’s kidney function had decreased.For the shy, timid person Catherine Duff was, the process seemed very intense.“The only thing they didn’t ask for was a DNA sample,” she says. ” Half an hour later, armed with a badge that allowed her to enter the NIH campus, she headed to the Lister Hill Center auditorium.In high school, presenting an oral book report filled her with dread. “I was horrified and I didn’t know what to do,” she recalls.At work, speaking in front of a small group of colleagues gave her panic attacks. “But I knew that the new policy meant more people were going to die.” All because they didn’t have access to a shot of healthy stool.The Food and Drug Administration was hosting a public workshop with a peculiar name: Fecal Microbiota for Transplantation.