All kinds of hepatitis C information



Hepatitis C is difficult to understand, and there are LOTS of "experts" out there who are more than willing to take advantage of the uninformed.  Please feel free to call our National Support Line for more detailed and personal attention related to hepatitis C (number listed above).

The folks who keep the NHCC in operation are unique people. ALL are volunteers who help fund our daily operations, tend to our telephone support lines, attend health fairs, and do just about anything necessary to help the NHCC continue to operate. These folks are required to have extensive and personal hepatitis C experience behind them before speaking to patients or family members about the disease, but this is just so we can make sure that what's shared is honest, trustworthy, and that our reputation remains stellar and accurate as always.

Times are difficult for most folks and money is tight. However, we too have significant expenses just keeping the NHCC in operation, and this is why it's so important that we reach out to good people like yourselves who will help us remain active for the "cause".

Please remember us in your prayers as well as with your financial contributions, and we promise that we'll do our very best to be here when you need us!

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Click on the graphic below for the press release and larger picture:

A discussion with Larry King about her need for kidney transplantation after only 4 mo. of hepatitis C treatments!


Jay's Story
(by Jay)

I My name is Jay. I'm 46 years old and I have Hepatitis C. It was diagnosed in 1990 at the University of Illinois in Chicago. Prior to that I had two heart surgeries, one in 1963 and one in 1985. Both of the surgeries were also at the U. of I. I had a biopsy done laparoscopically, because I take an anti-coagulant, Coumadin, plus, (as you all know), my platelet counts are wacky. After I was told I had hep C and cirrhosis, I was stunned. All I could say was "doctor, I don't drink that much". He assured me the cirrhosis was caused by the hepatitis and due to all the scarring, they figured that I probably got it in 1963 from my first surgery.

I said "how could I walk around with this illness for so long and not know it?", and he said "That's why they call it the 'Silent Killer'"!!! I asked what about my wife, they said then that it was not sexually transmitted. Somehow though, it was too late, she had it too by then. At least it lifted a burden of one sort because in 1985 they had just started screening blood for the AIDS virus. I cannot express my feelings in words for feeling like I somehow gave my wife this monster, but if it would have been AIDS, I couldn't live with that! She has been a trooper, helping me fight Social Security for my disability. There aren't too many people I know that would do that, even married couples. She's a very special person to me and I love her very much. But now I'm waiting to go on the combo treatment. I have been through interferon twice. With my first regimen, it worked very well. I felt great! Like I was a high school kid again, but I screwed up. The second time I felt lousy so they took me off of the interferon that time.  That was two years ago. So here's hoping that maybe after another try, this will work.

P.S. Did you know that dogs are immune to Hep C? (That's something to think about)


The opinions expressed on this page are solely those of the author and none of the information included is to be misconstrued as medical advise.

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Last Updated March 20, 2012