Fecal Transplantation trial

I may be able to participate in a randomized controlled trial of fecal transplantation and just wonder what others with UC think of this. I put my name in a while ago. The study is being done at a major teaching hospital that I have total faith in. I would be given the transplant enema once a week for 6 weeks, with testing at the beginning to see what bacteria is in my gut and testing at the end to compare. Not sure of all the details yet, I am still trying to make up my mind, but must let them know soon.
The thing is I may be heading for remission now. I have partially formed stool and no blood or mucus. However I still have abdominal pain and spasming. I just started to have maybe one or two good days out of a week, as far as abdominal pain/spasm go. I also know that next week I could be back into full flair, it is UC after all.
I know that only I can decide, but many people on this forum do a lot of research and I would like some input.

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Diagnosed with pancolitis October 2013
2400mg Asacol(Generic version, 5- Aminosalocylic Acid), taken in two doses of 1200mg
80mg Tecta(pantoprazole magnesium), taken in two doses of 40mg
Vitamin D and B12
B12 injection every 2 weeks

Diagnosed with Hiatus hernia 2012
Gastritis, twice a year(approx.)
Uveitis, last flare was 4 years ago
Fistula surgery next to anus 15 years ago
L2 spine burst fracture in 1998, from injury in 1998
Chronic pain

Do it. This isn't like a new med with who knows what side effects. Even though this wouldn't be guaranteed 100% safe, I don't think you could get much closer. There is really very little downside.

Yes! Please share the details as to where it is. I'd love to give this a try....Sign me up!

Given ur current 'limbo' state symptom wise, I'd do it. If, however, you were symptom free with medication, id wait they do more research on the procedure. You can always have FTs done in the future if they prove to be truely successful.