By taking just an hour of your time to participate in the HepPRN patient registry, your information will make a difference in bringing hope, new treatments and better outcomes for people with hepatitis.
Take our survey (you can start it and come back as many times as you need to finish it):
The Hepatitis Registry Network (HepPRN) securely collects health and lifestyle information regarding the lived experiences of those affected by or infected with viral hepatitis, by using a highly protected and private survey. It is a very interactive survey that gives you feedback as you go along.
The result is that the data will be available to medical researchers selected by Hepatitis Foundation International, but allowed to see the de-identified data by you. Researchers will be able to contact you to participate in research and clinical trials if you select that option.
The #HepPRN registry was created by HFI International with input from our patient community. Please set aside an hour or so to do the survey. You do not have to do it all at once.
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