Anyone post liver transplant doing the incevik?

[Kat4Kurt]

Hi, my name is Kathie and my husband had a living donor liver transplant 2 1/2 years ago.  He now needs to start treatment to keep the Hep C from damaging his new liver further.  Would like to hear from anyone post transplant concerning their treatment for the Hep C.  Thank you!

[Kat4Kurt]

Thanks for the prompt replies.  My husband has not started taking the incevik yet, but, started the first phase of the treatment with the interferon/ribavarin about a month ago.  He is due to start the incevik next month.  Over the past 15 years he has done many trial treatments to no avail.  He has been a non responder.  Thankful to find this site and be able to ask/answer questions that may help us/others :)

[Kat4Kurt]

Thanks so much!

[orphanedhawk]

Hi,
I had a live liver transplant in April 2009. In August my biopsy was stage 1 bridging to stage 2.
So, in October, I began standard, interferon/ribavarin treatment for hep C. I am genotype 2.
So far the treatment is working well. My side effects are much more tolerable than when I did the treatment prior to my transplant.
I've had two undetected viral loads, at 4 and 8 weeks.

Please feel free to send my a private message if you have any questions.

Good luck,
OH

[can-do-man]

Just saw the incevik part, OH is just on SOC, though you still might get her insight.

[can-do-man]

Hi, we have one menber here who also had a living donor transplant, she is now doing treatment.... She goes by orphanedhawk. You will see her name to your right under Top hepatitis Anwserers. Just click on her name and you will see "send message"

I'm sure she would be glad to offer any help.............. Best to you.