As I mentioned in the post above from April 13, 2016, Rifaximin might make him feel better right away. But FMT (fecal microbiota transplant) is a miracle cure for C. Diff. It is used to treat persistent reinfection and it works! We had to go to the Rochester, Minnesota clinic to get it because that's where their pediatric GI clinic is. Not sure if other doctors do it in AL. You might try Rifaximin first if your doc will prescribe it. We saw fast relief, but we got on it 3 wks before the transfer and then we were home free. It's a lot of expense to go to Mayo, but once you get there, you will be so relieved. My daughter has been healthy for 3 years now, and life is great. Though any tummy upset makes me worry, she's never had a relapse. We avoid anyone on antibiotics and i use a lot of industrial bleach around the house, but so far so good!

The most important thing is to persist. Some doctors tend to think "kids are resilient" and are content to let things drag on. You need to insist on the best possible treatment until he's better. He does not need to suffer and it's a dangerous infection that needs attention. Hang in there and get a new doctor that specializes in C. Diff.

Last, Flagyl and Vancomycin work on C. Diff but they are awful on your body. Rifaximin was gentler and effective. But the FMT is the lasting cure. Online school is a good option if he's too sick to attend. Many school districts have to provide it if the student has medical reasons for missing school. Advocate, persist, and take care of yourself. You got this!

I also just found this info from an email I received from a doctor in Alberta, Canada, Thomas Louie, who creates pills from the FMT donor. I wrote him years ago to ask him to take us as a patient, but here's more info: "There is a 60% chance of escape from recurrence with rifaximin, so let’s hope it works. It needs to given for at least 14 days, prefer a bit longer. Fidaxomicin also offers escape, but peds indications not there yet, though there is no technical reason why one cannot take it. Used as a taper by stu Johnson in Chicago." Hope this helps--at least you have a couple Rx's to try. There have been articles written on his work, so you might research him. Many hospitals have research libraries open to the public, so they might be a resource as well.

Hi @tammy1pike! I am from the North Alabama area and my daughter attends college at a major university in Central Alabama. This is her 3rd round of cdiff in 1 years' time. We literally got the results back this morning and when I expressed my concern that this is her 3rd round, the doc office nurse suggested that maybe she see an Infectious Disease Specialist. We will be setting her up with a new GI doc near her college town after the first of the year and will also look into Infectious Disease doc down there as well. While I don't have anything useful to add to the discussion I would just like to connect via this route and gather info on everyone else's experiences. Hope your son gets better very soon.

@breed28 Hi! So sorry to hear about your daughter’s CDiff Infection! It is horrible on the patient and on us, as parents! Since my post on Mayo, I researched and finally found a wonderful doctor for my son. Her name is Dr. Keta Vaidya and she is at Digestive Disease Center in Huntsville, AL. My son had already taken a round of Flagyl (which made him sicker than the actual C Diff), and he took Vancomycin next which offered temporary results. On Dec. 21, my son had a Fecal Microbia Transplant at Huntsville Hospital by Dr. Vaidya. It was simple, hassle-free, pain-free for him and was an immediate answered prayer!! After recovering for about an hour (to let the new, healthy feces absorb into his colon and redistributing good flora bacteria, he was a different child! His smile came back immediately and he even ate a steak dinner on our way home! He has not had one C Diff symptom since. Now, he is working on weight gain. He lost 40 lbs in about 8 weeks so he has a road ahead but is great! Please consider Dr. Vaidya. She is remarkable! Best wishes and thank you for your inquiry. Prayers that your daughter feels better quickly! This disease is not to be taken lightly. Let me know if I can help.

Welcome to Connect @breed28. Sharing your or your loved ones' health journey is one of the most valuable aspects of this Connect community. It helps to know that you're not alone - thank you for telling us about your daughter.

@tammy1pike, we are so happy to know that your son is feeling better! Fecal transplant is a rapidly emerging therapy, and I'm certain fellow Connect members would appreciate learning more about it; would you be able to share a few details? How long did the process take? Did your son have to undergo any "prep work" before the procedure?

@kanaazpereira.... There really aren’t many more details to give. The Fecal Microbia Transplant was the same prep as a Colonoscopy. So, the day prior, the patient does a colon cleanse which was not fun because the liquid my son drank made him vomit. However, in hindsight it was worth it all. On Dec. 21, 2017 we drove 3 hours to Huntsville Hospital for my sons Fecal Transplant appointment at 7am. It was a smooth, fast procedure. It took maybe an hour because Dr. Vaidya checked his colon for ulcerative colitis as she inserted the device. Then, as she removed the device, she injected about a 12 ounce-can size amount of donated feces from a healthy patient. Of course all donated feces is tested and screened. (Watch Youtube videos to learn more. I did.) Afterwards, my son was in recovery, sedated, for about an hour so the healthy feces could absorb into his colon and allow healthy bacteria to re-colonize in his gut. After my son woke up, he was released from the hospital. It is an out-patient procedure that is fast, painless, and was immediate relief for him! He never complained of pain or discomfort. He even ate a steak dinner on our way home. He has not had one C Diff symptom ever since and today is Day 10, post-Fecal Transplant! Digestive Disease Center in Huntsville, AL; Dr. Keta Vaidya is his Doctor’s name. They are phenomenal! Please contact me if needed. Prayers to all of you dealing with C Diff Infection!! My son lost 40 lbs. in about 8 weeks due to C Diff (re-diagnosed after taking round 1 of Flagyl). He has a long way to go! He was a nearly 200- lb. baseball player. Now he weighs in low 160’s. Please keep him in your prayers as he recovers. Thank you!

Hello everyone! I thought I would update you on my son’s progress. As I stated, he had a Fecal Microbia Transplant on Dec. 21, 2017. On our way home from this procedure he ate a steak dinner after not eating for weeks. He then would eat one meal per day, most days until about January 15, 2018 (11days ago)! Suddenly his appetite returned full force! This gave his body much needed fuel! He returned to Varsity Baseball Practice last weekend and has gone everyday since! He now feels much better! His focus is on catching up on his school work and on rebuilding muscle that he lost dyring this C-DIFF illness! He is down 40 lbs. from the first 7 weeks of showing C-DIFF symptoms. He lost muscle and was severely malnourished. However, this should give hope to anyone else out there with C-DIFF! Get control of your/your child’s treatment plan! Get involved! Pray for wisdom and for guidance! This helped me find Dr. Keta Vaidya at Digestive Disease Center in Huntsville, AL! Other doctors planned to keep prescribing multiple rounds of Flagyl and Vancomycin after my son’s C-DIFF reoccurrence. My son had no weight left to lose! He was skin & bones! My point is, you have the right to change your child’s treatment plan if you need to! Prayers and best regards to you all! Thank you to those who private messaged me about C-DIFF! It is nothing to take lightly!

Thank you for the information on a treatment I never heard of this treatment,a friend of mine has come down with C-diff I will pass on this information Again thanks

Don't take no for an answer. Flagyl is horrible, it's a cheap drug, that's why they prescribed it so much. My platelets bottomed out on it. Have blood work done on him, check his platelets. Vancomycin is better. Definitely take S. BOULARDII, it's a game changer.in canada we have Florastor and Renewel..