National Hepatitis C Program

This pamphlet outlines information about viral hepatitis. The pamphlet explains hepatitis A, B, and C; what it is; how it is spread; symptoms; treatment; and prevention.

This poster states that it takes two different tests to diagnose hepatitis C. One test is a screening test that indicates whether a person was ever exposed to hepatitis C. The other test is a confirmatory test that indicates if a person currently has hepatitis C.

This pamphlet provides information on how veterans can cope when they have been diagnosed with hepatitis C. Some of the most common feelings associated with a diagnosis of hepatitis C are the following: sadness or depression, anger, fear, and anxiety. The pamphlet gives information on how to take care of your emotional needs, including talking about your feelings with your doctor, friends, family members, or other supportive people.

This information sheet describes good nutrition as being of great importance to a person with hepatitis C. It provides guidelines for healthy eating and drinking. It advises the following: Do not drink alcohol, avoid crash diets and/or binges, educate yourself about nutrition, eat a variety of foods, and drink plenty of water. It discusses overcoming barriers to eating well.

This information sheet discusses the liver biopsy. It explains a liver biopsy; the risks involved; how a liver biopsy can help, particularly for people with Hepatitis C; how it is done; and what happens after the liver biopsy is done. It also discusses when one should not have a liver biopsy. The information sheet specially emphasizes that a person who takes medicine for hepatitis C might need to have more than one liver biopsy.

The purpose of this pamphlet is to let patients know what they can do to keep their livers healthy. It contains information about liver health lab tests, the virus and how it is spread, hepatitis A and B, sex and hepatitis C, and hepatitis C treatment. The guide also includes some useful resources for patients.

This information sheet explains how to get treatment through a clinical trial for the hepatitis C virus. It explains how clinical trials work and what the different types of clinical trials are. It discusses informed consent, cost, how to find clinical trials, and the benefits and risks of participating in a clinical trial.

This information sheet urges people with the hepatitis C virus (HCV) who want to try alternative treatments to follow these guidelines. Patients are encouraged to: check with their doctor first; see an expert; and beware of false promises. Talk to people who have been to an alternative treatment expert in the past to be sure the expert has a good reputation, licenses, and certificates. False promises, such as certain herbal remedies, supplements, certain vitamins, or "natural" medicines, can be very dangerous for people with HCV because they may hurt the liver.

This pamphlet explains basic facts about cirrhosis, which is a disease of the liver. It can help patients understand the causes and treatments of cirrhosis. The pamphlet answers patients' questions about common complications of cirrhosis and provides information on how to deal with these complications. It also provides practical tips on how to keep a patient's liver as healthy as possible, including things to do and things to avoid.