Hepatitis C Support Group
Hepatitis C is a blood-borne viral disease which can cause liver inflammation, fibrosis, cirrhosis and liver cancer. The hepatitis C virus (HCV) is spread by blood-to-blood contact with an infected person's blood. Many people with HCV infection have no symptoms and are unaware of the need to seek treatment. Hepatitis C infects an estimated 150-200 million people worldwide.
For some reason or another that url isn't connecting me to the story... Instead it will cause mt browser to show a search result with the links to various "Daily Press" news websites from all over the USA that offer a very wide variety of news except for that story...
Could you please re-post it so that I can connect to it directly?
You Ozzita, I also have an interest in this story as well. ;>)
Respectfully,(For the most part ;>) )
HANK
Let's see if this url works better for me... Thanks anyway. ;>)
http://www.dailypress.com/health/dp-nws-clinical-trials-0425-20130426,0,6645498.story
HANK
Interesting facts involving this story which is totally different than mine although I can still relate to some of the stuff he has experienced...
For instance:
1.) He's a living donor recipient which in itself is being better off when it comes to the dosage requirements of immuno-suppressant, anti-rejection drugs because the living donor is a much more compatible match requiring a lower dosage of the anti-rejection drug he's on...
I take a larger dose since I received a complete liver, and that means that they would have to significantly lower my anti-rejection drug (I'm on Tacrolimus otherwise known as Prograf) to very dangerous levels which could cause organ rejection during tx...
After over 15 years post-transplant, I didn't want to take the chance of organ rejection for the first time due to being on triple tx and that's another reason why I opted not to go in one of the same clinical trials as this gentleman did...
I don't know if this gentleman is on the same drug as I am since the article doesn't describe that detail... I do know that if Marilyn does the triple therapy with victrelis and the fact that she's on cyclosporine as her anti-rejection drug, they will not have to lower the dosage as much with her compared to what my transplant team would have to do with me...
2.) He has only been on Ifn therapy once prior to his transplant and I don't know whether or not he also took ribavirin... I was on Ifn therapy @ least nine times, and quite a few times post transplant...
3.) I had the transplant over 15 years ago... He had triple therapy w/Telaprevir roughly three years after his transplant which is very similar in time frames as Marilyn's own experience has been post transplant...
4.) Both Marilyn and this gentleman will have their triple tx as their first time being tx post transplant and for Marilyn, it would be her first time treating ever! I was treated with combo tx (SOC) if I remember correctly 4 or 5 times post transplant to no avail yet. ;>)
5.) Post transplant patients who have had the virus return tend to be more successful in achieving SVR if they treat shortly thereafter than with patients who have been post transplant for over 10 years or so and have not been as successful in previous attempts. :>(
6.)I was SVR twice for over two years and post-transplant also but, I developed mutations of the virus which now makes Ifn tx no longer effective and would make the triple tx ineffective also as well as being even more very dangerous for me!
7.) He's more fortunate than I was as far as false alarms go while waiting for the gift of life... He had three and I had seven! Now I don't know if Marilyn had any but, I'm sure she'll chime in once she read this story. ;>) Nonetheless, it was a great story!
Thanks for the story Kramer! ;>)
Respectfully, (For the most part ;>) )
HANK