# Reoccurence PSC 3 yrs after transplant

**URL:** <https://forum.livingwithpsc.org/t/reoccurence-psc-3-yrs-after-transplant/187>\
**Category:** Life with Primary Sclerosing Cholangitis\
**Created:** [August 5, 2013, 8:19pm UTC](https://forum.livingwithpsc.org/t/reoccurence-psc-3-yrs-after-transplant/187 "2013-08-05T20:19:37Z")\
**Posts on this page:** 1\
**Page:** 1

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**Author:** ![Catherine\_J\_L](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithpsc.org/catherine_j_l/32/258_2.png) [@Catherine\_J\_L](https://forum.livingwithpsc.org/u/Catherine_J_L)\
**Post date:** [August 5, 2013, 8:19pm UTC](https://forum.livingwithpsc.org/t/reoccurence-psc-3-yrs-after-transplant/187/1 "2013-08-05T20:19:37Z")

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Recently I was diagnosed with reoccurence Small Bile Duct PSC. Have been itching since Feb. 2013, and subsequently have increased my antirejections to almost the level I was on after TX in 2013. It has helped some along with a variety of meds to help with the itching...I found some information in the net regarding the useage of a Probiotics and Prednisone and/or immunosuprressive therapy that has helped children, which has either stopped or reversed the progression of PSC. I have been trying to convince my doctors at UCSF to let me try vancomycin but they are very reluctant or resistant to letting me try it...So I was wondering if anyone out there has been able to try these two drugs and what the outcome was....Appreciate any info on this...Thank you