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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!


Walt's Story
(by Walt)

Hello,  My name is Walt I am 42 years old I have hep C genotype 1b, LFT's slightly elevated, biopsy show's bridging portal to portal fibrosis with necrosis. At the age of 17 I entered into service with the U.S Army therein I was trained to be a medic between the years of 1976 and 1983. I contracted hep C. In 1990 I went to donate blood I received a letter that changed my life. The letter went on to say you need to see a doctor . Off I go to the Dr. who does a cursory exam and asks some risk factor questions and say's your only factor was working emergency rooms but you have nothing to worry about.

Fast foward to 1996 after having pain in my liver area for about two months I once again went to the Dr. who does the labs and comes back at the next visit and states you have hep C we need to do a biopsy. After those results came back I then realized the fight I was now undertaking was not one of simple rest and recovery. I went from a pretty active fellow to one troubled by chronic fatigue  joint pain  liver pain skin rashes colic gall stones depression . I figured I needed to focus my energies on my future security and my families well being. I began my appeal with the veterans administration I was initially awarded 10% rating, I appealed that rating and was awarded 100% in Feb 2000.

In August of 2000 I took a medical retirement from my job at the Postal Service. I am fighting my last battle with SSI. In hind sight I am glad I undertook these fights with three governmental agencies while I still had some energy because even now I am a shell of what I was a mere four years ago . My support system has been great, my wife has taken a huge burden on herself by picking up a lot of my slack as we raise our four children. This in itself is amazing considering the old adage "you look good, ya must feel good," ha. The biopsy it didn't lie.

My wife is currently finishing her masters deqree while working part time and being a mother and nurse and wife. The people who I considered friends have all slowly vanished - some faster than others. I find spiritual solace in the Lord and the Holy Bible and I find emotional solace in my family. I get bummed some days until I see my seven year old daughter , there I see in her eyes energy, hope and a care free feeling that all is good on this earth.

So that my friends is my tale and I am sticking to it .


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Last Updated March 20, 2012