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Hepatitis Message Board


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Board Index > Hepatitis | 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z


I have been a member of this health board for awhile and I can readily relate to everyone's predicament when it comes to Hep C. I have unsuccessfully underwent Tx twice and have some side effects from that also. What I have not found here or anywhere else is a group of people I can exchange info with which is more pertinent to my condition. I was diagnosed with Hep C approximately 4 years ago. My liver was in stage 4 failure, extremely cirrohtic. I was the lucky beneficiary of a liver transplant about 3 1/2 years ago. Like most people with HCV who have to get a transplant before they can undergo Tx, I still have HCV. There are similar problems with people who have HCV but mixed with the problems brought on by the transplant and the meds I have to take, my physical condition is unique in a few ways. Do anyone out there know of a place where transplant patients who lost their liver to HCV and who still have HCV post their messages? In particular, I am very interested in life of a transplanted liver when HCV is still present. Everything I can find to read and talking to my Dr. the average life of a transplanted liver in this situation is 8-10 years. I realize everyone is different but I would love to hear from someone who has a liver transplant > 8 yrs. and has HCV.





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