Just wondering if this has happened to anyone on here.. I suffered from c diff after two rounds of antibiotics. Undiagnosed for months because my GP and GI doctor he sent me to said it was IBS. Luckily I got a new one and she figured it out at my first visit!
Anyway… I still have not gotten back to normal (7 months later), and a calprotectin stool test shows me at “borderline” by about 12 over the “normal.” All blood tests have come up normal as well.
Anyone else develop colitis from c diff? I’ve read articles that it’s possible. My symptoms are all over: looser stools, mucus in stool, lower right stomach cramps and pains, undigested food in stools, back pain, bloating, pain after eating, and borderline inflammation.
I’m not running to the bathroom throughout the day, I go once in the am. So I keep getting told it’s normal. I don’t feel normal. Very frustrating! I obviously don’t want more problems, but if I have them, I’d love to start the process of trying to feel somewhat better.