Please help I've had clostridium difficile colitis for years untreated.

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Hello My name is amanda! I am 26 and I had my gullbladder removed in the fall of 2014. Because the surgery was an emergency i wasn't in an out within a day like a normal procedure. I Stayed in the hospital for a week. i believe that is where i contracted the C diff infection. since i was having watery stools 8-10 times a day i assumed it was from having my gullbladder removed my surgeon told me that watery stools would happen until my body was used to and addapted to my gullbladder being gone. For years i just assumed this was my new normal. The terrible stomach cramping, Bloating, Bloody stools, Watery stools all day every day, fissures, hemorrhoids and the vomiting were just some of the things i experienced on a daily bases. Since I was having other medical problems around the same time that all of this was going on I just put all of my stomach symptoms on the back burner and just started "accepting" these as the new normal for me. 4 years later and still having the symptoms after I got the other medical things taken care of. I decided it was finally time since the symptoms were as worse as ever to figure out what was going on. I was put on different medications and told I had IBS because of my surgery for another year I tried different medications that in return just left me constipated and the cramping even worse. Yes it took care of the watery stools but the constipation was so bad that I stopped the meds and delt with the diarrhea ( since it felt better to let it out then hold it in and be constipated) once I told My primary care doctor that I had enough he sent me to a GI specialist. They did a Stool sample and that night the on call doctor from the lab told me I had the C diff infection. 4 years of the same symptoms worsening. I finally had answers!! My GI specialist put me on a 10 day round of Vancomycin 125 mg 4 times a day. I was tested again after I finished the round of antibiotics. And yet again tested positive for the C diff infection. My Doctor told me she was going to put me on another round of the same antibiotics but for 3 months this time. She said if this round doesn't work she wants me to get Fecal microbiota transplant. I am hoping this round will work though. I've searched the internet for anyone that has gone through c diff for this long. The only stories I have seen are of people that took antibiotics and got C diff from that and have only had symptoms for 4-6 weeks. I'm looking for anyone that has had it for years I'm nervous what my colonoscopy will show since I've had it for so many years. I'm hoping there is not to much damage to my insides. I'm open to any and all suggestions a long with personal experiences with C diff thank you in advance for all of your help!

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3 Replies

  • Posted

    This sounds like my story. i had sepsis from my gallbladder and as a result had a takutsobu heart attack ( stress heart attack or broken heart syndrome) which i thought was a virus and waited 3 days to go

    to hospital as i had numerous gallbladder tests previously and told they were normal.

    Since the surgery, I've had the same issue with continuous daily multiple bouts of diarreah with times just coughing causing me to lose stool and cannot count how many panties I've ruined. went to Gastro and they said a lot if people get this. they gave me a prescription that did work a little but then stopped working. i now keep

    immodium on hand and if i need to go anywhere i use it.

    i had a colonoscopy last November and everything in there was fine. Although i now have an internal hemmorhoid i never had before. i can only guess its from the

    constant loose watery stools. I was told to use metamucil but that is a laxative and I have more problems if i use those because I can't stop going. I was just in the hospital and they kept trying to give me stool softeners and I said are you crazy? i sure do not need that. I had the antibiotic caused C DIFF before too but yes, once i was off the antibiotics it ran its course.

    i am still in search of finding what helps as well.

    If you research online about gallbladder and diarreah you will find lots of people experience it.

    MY Gastro Dr. said its because your stomach acid is now too high and the gallbladder used to take care of that. main things that you could eat before you have to figure out what sets you off. I know i can not tolerate oils now so i got an air fryer so i do not have to fry food any more.

    Day by day i find out what i can not eat.

    It's a lot of trial and error. I get nausea a lot too. Mainly keep aware of what makes you sick and avoid it.

    there are gallbladder diets.

    • Posted

      Adding, I had my surgery 2016.

      I am 63 and this is truly a frustrating thing to deal with.

      I now carry extra panties in my car. And always carry pads as well.

  • Posted

    Hi just wondering how did your colonoscopy turn out to be like???

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