The CHI (Charting Health Impacts) Study is about the impact of hepatitis C on peoples’ lives. The study follows a group of people over time – looking at all the health and social aspects of life – so they can tell community organisations, doctors and governments what it is really like to live with hepatitis C.
Joining the study involves taking an anonymous online survey, which you can take your time completing. We then contact you in three to six months so you can tell us how things have changed for you.
If you have ever been told that you have hepatitis C (even if you have had treatment since then) and you are interested in participating in the study, or if you just want to find out more about the project and hepatitis C, you can access the Chi Study here.
Please be sure to let your experience count and let us know about how hepatitis C has affected you.
Check out the website at www.chistudy.org.au