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!


Valene's Story
by Valene

Hi my name is Valene. I was born with a lung disease, which required blood transfusionís and now, I am living with hepatitis C, cirrhosis of the liver, and other medical problems which I have suffered through for the past fourteen years.

I thought I was doing good until I went in for an A.D.D research. I had blood drawn and found out that I had high liver enzymes. My pediatrician said that I had mono and possibly hepatitis C. He referred me to a specialist, Doctor Rothbaum. I had a lot of tests done and I could not believe it when I found out that I had hepatitis C and cirrhosis of the liver. even though I had no idea what it really was, I knew I was dealing with something very serious and my life was going to be turned around.

I started the combination treatment. it was so upsetting to find out that my parents and me would have to give me my shots at home. I had to take three shots a week and six pills a day for the past four 1/2 months. I got so strong that I started giving my shots to myself. The treatment was so hard on me that I had to stop schooling, and get home tutoring. I am dealing with side effects such as, flu like symptoms, aches, pain, crying, bruises, thinning of the blood, excessive tiredness, terrible itching acts, female problems, and being treated for depression. I am seeing three to four different doctors at this time for related problems.

I was hoping under the will of God that it would cure me, but I found out that it was not working. I have stopped the treatment at this time and attending school again. I am in rare case of hepatitis C and cirrhosis of the liver. I live with the fear of knowing that the hepatitis C is still very active in me. There is no cure and I canít do anything about it, so I pray day by day that there will be a cure for hepatitis C. I now wait and wonder if I am getting better or worse. I am so young to be going through all of this without any hepatitis C support groups for my age, but I do the best I can with Godís help. I want to thank my parents for being there and struggling through it with me. I love you Mom and Dad.
Thank U


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Last Updated March 20, 2012