C Diff

Posted by TiaraDee @tiaradee, Jul 11, 2012

I first got sick on May 1st thinking it was the stomach flu. I weight 157lbs and every er that I went to told me to sleep it off and that the longest it could last is two weeks. Two weeks later no difference. I finally saw a gastroenterolgist sometime in June. At that point it was 1 month of no appetite, nausea and diarrhea with tons of mucus(sorry to be so graphic). I did a stool test and he said I had inflammation somewhere and to eat bland and it would go away. It didn't so finally he said I could have Giardia due to having yellow poop since march 🙁 so he put me on flagyl and ciprofloxacin. I guess I put all my eggs in one basket and hoped and prayed that would be it. I started feeling better until one day after I ate I had the urge to throw up. No nausea or anything. Finally had a colonoscopy on June 19th. Got diagnosed with C. Diff colitis. He put me on flagyl three times a day for two weeks. I had my good days and bad days. Fourth of july came around I had a hot dog and pasta salad and that's the last day I ate something delicious. Since that day I've felt horrible. I finished my antibiotics that Saturday and I've become worse. All I taste is blood now. Anything I drink makes me want to throw up. I have to sleep sitting straight up :(. I'm miserable and I currently weight less than 120. So to go from 157-120 in a matter of two to three months is taking its toll on my body. I'm losing hope. I'm 22 years old and Monday April 30th was the last time I was actually happy. If anyone has information or anything to help me please respond. I know I could have something way worse but to go from being perfectly healthy to being labeled anorexic because you want to eat but you can't is really hard. I'd love to hear other peoples stories on this horrible infection.

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Profile picture for sanfan @sanfan

I see this was posted in 2012. If you are still active on this subject I'd like to know how you are now. I've been suffering for 8 months and getting no answers after C Diff.

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@sanfan Vowst is a good medication as well as DIFICID. DIFICID is an antibiotic to get rid of C-Diff but very costly. Two pills ten days and your done.
Vowst is healthy poop in a capsule. Both will work. Vancomycim as a liquid that slows down the infection but does not cure it.

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I had my gallbladder removed many years ago, but i ended up with a gallstone stuck in my bileduct. Eating was very painful. I found I could eat fish, Hawaiian rolls, fruit but without skins or seeds, and chicken stuffing but I had to pick out the celery. Ultimately I lost 70 lbs in two months from starvation. Although I wanted to eat and I did try. Pain is a great deterrent even if you are hungry. Be careful not to eat to much salt water fish. No more than 3 ounces 2x per week.

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DIFICID is an antibiotic designed for C-Diff. Also Vowst is good to.

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Profile picture for hoagie @hoagie

Both my wife and I had cdiff. I got it through contact with her. She had it multiple times. And was hospitalized several times. I had it 3 or 4 times. And was treated in the hospital I found out with an online search about cdiff that there's a treatment for it. The hospital that she would go to knew about the treatment. But wouldn't do it. I guess because another hospital developed the treatment in Boston. We decided that she would transfer all her care to the other hospital. She had been through enough already by that point.

The treatment is called a stool transplant. It sounds gross. But it worked for the both of us. They take a stool sample, bring it into a lab. Treat it some how or other. They put it into a gelcap pill. On dry ice. The patient swallows it and within a few days. That sample changes the bad bacteria in your gut to good bacteria in your gut.

There's always a chance that you could get cdiff again from what they told us. But that never happened to us.

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@hoagie I might mention that I also had it and as a patient of Mayo Clinic in Phoenix also treats CDiff with that same procedure. I was advised about it but luckily mine responded to the initial treatment and now 7 years later I have not had it return. So there are other hospitals that also do that procedure.

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Profile picture for Dana, Volunteer Mentor @danab

@hoagie I might mention that I also had it and as a patient of Mayo Clinic in Phoenix also treats CDiff with that same procedure. I was advised about it but luckily mine responded to the initial treatment and now 7 years later I have not had it return. So there are other hospitals that also do that procedure.

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@danab My cdiff hasn't come back in over 15 years now. I hope it stays that way.

Thank you

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Profile picture for feeble6tress @feeble6tress

have you tried the holistic aproach. go see a nutritionist if you can because one thing i have learned is that only one out of hundreds makes to much stomach acid. the heartburn or what they call "gerd" is usually from to little acid. I am extremly ill and down to 100 pounds and i cannot eat. ive been drinking smoothies with protien and vitamin powder. have had several test and yet to have a diagnosis other then ibs when i know thats not what it is. this week i will be swallowing a camera pill so that they can look at my small intestines since they couldnt find anything with the colonoscopy and the upper endoscopy but i do know that one of the big problems was from taking ant acids for far to long. So my nutritionalist put me on a suppliment called gastracid and digestive enzymes. and it did help. now i no longer eat enough to take them but will again when i am able to get back on solids. i can really relate to what your going through. my pain is constant and i am now so mal nourished i can barely function and its making me incredibly anxious. one thing that helps with the pain is achupuncture. id definatly look into alternative meds because eastearn medicine and drs have been around far longer. and western docs are simply so obsessed with money. in the medical society if your not wealthy you dont deserve to be healthy. i hate it so much and feel quite hopeless at times.

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@feeble6tress I had Cdiff 4 separate times last year and was in the hospital for a total of 30 days. It is a horrible disease and really takes a toll on your body. I was given Vancomycin by IV each time and it did work for me. But as soon as I got home from the hospital it returned. My Doctor got the approval for Vowst, a fairly new medicine for Cdiff. It was very expensive but I decided to try it. Unfortunately it did not work for me and I got sick again after completing the prescription. (4 pills). I was put on Vancomycin capsules after the last episode. 4 pills a day for one month, then 3 pills per day and so on. I am now taking 1 pill a day for six months and am feeling much better with no issues. Prayerfully once I stopped the pills I won’t have a relapse. It was a real struggle for me and at times I thought I would never feel good again. My Doctor really worked with me and understood what I was going through. I hope you will be feeling better soon.

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Profile picture for joanns21 @joanns21

@feeble6tress I had Cdiff 4 separate times last year and was in the hospital for a total of 30 days. It is a horrible disease and really takes a toll on your body. I was given Vancomycin by IV each time and it did work for me. But as soon as I got home from the hospital it returned. My Doctor got the approval for Vowst, a fairly new medicine for Cdiff. It was very expensive but I decided to try it. Unfortunately it did not work for me and I got sick again after completing the prescription. (4 pills). I was put on Vancomycin capsules after the last episode. 4 pills a day for one month, then 3 pills per day and so on. I am now taking 1 pill a day for six months and am feeling much better with no issues. Prayerfully once I stopped the pills I won’t have a relapse. It was a real struggle for me and at times I thought I would never feel good again. My Doctor really worked with me and understood what I was going through. I hope you will be feeling better soon.

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@joanns21 According to a world renound infectious disease doctor Vancomycim only gives a false negative. It does slow it down but it does not cure C-Diff. Word seems to spread much to slow to be of much help. When a person takes certain types of Antibiotics either by IV or pill form, C-Diff is often the outcome.

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Profile picture for mrsjohn101 @mrsjohn101

@joanns21 According to a world renound infectious disease doctor Vancomycim only gives a false negative. It does slow it down but it does not cure C-Diff. Word seems to spread much to slow to be of much help. When a person takes certain types of Antibiotics either by IV or pill form, C-Diff is often the outcome.

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There is a newer antibiotic, Fidaximicin that works only in the intestine and is not absorbed nto the bloodstream, That, in combination with Florastor probiotic ( contains a yeast that helps flush out the Cdiff and is not killed by the antibiotic) seems to be very effective. My husband is doing well. We will see what happens over the next few weeks. The Fidax stopped the diarrhea in 2 days!

Sent from Yahoo Mail for iPhone

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There is a Foundation called Peggy Lillis please connect with them. They are all about keeping people informed about C-Diff and education on current benefits of medications.

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I'm no doctor, please see an infectious disease doctor. Through my own personal experience, the mucus sounds like fatty liver disease, blueberries will heal that along with good nuts. Fatty liver can be caused by a gallstone in the bile duct/via from not eating.
As for the C-Diff, it is induced by antibiotics. To many antibiotic kills off all the good bugs and only leaves room for the bad bugs. Vowst should take care of that. Please see an infectious disease doctor.

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