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 HERE FOR NATALIE COLE'S VIDEO INTERVIEW
A discussion with Larry King about her need for kidney transplantation after only 4 mo. of hepatitis C treatments!

 


Barbara's Story
(by Barbara)

Hi! 
My name is Barbara and I have probably been a victim of hepatitis C since 1978, if not before. I have been ill all of my life and at the age of 15, in 1978 (yes, a woman confessing her real age...LOL) I went into liver failure and stayed there for several months. And for the rest of my life I have fought the dreaded physical pain that comes with severe liver failure. I was severely ill in 1990 but docs and hospitals at the time would not touch me. I was considered a street person. No one wanted to touch me. They thought I had AIDS and turned me away. 

My hep C diagnosis came in 1997 when I went to donate blood. at first I thought it was a joke. I could find nothing of significance on it.  But I knew something was wrong. I had always had periods where life just seemed to change. I am normally high strung so to speak and was raised with a work ethic of if the other guy is working twelve hours a day, you work fourteen. You can always be replaced. The fact was it was getting to the point where I didn't care if I was replaced or not. It was hard to bounce back whenI drove my body too hard. Several hours of needed rest was becoming several days. 

Fact is hep C took away my life. Yes, I did the interferon and from what I know now...there is no way I will do it again. Not only did it destroy my health but it hurt my heart and soul. How does one live when one isn't able to work? I am single. How does one date or get support? I have recently started a support group that hopefully will help heppers.

If any reading this have any questions or input, please email me at babylonia1@juno.com 
Let's fight the dragon together as a community....even more...let's get the community to help us fight the dragon! (how quickly they forget that at any moment it could be them who are about to lose everything!)
Barbara

 

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