Hep C Action Aotearoa is jubilant that a treatment that works for all types has been approved, available from 1 February
2019.
With treatment soon available, the focus shifts to testing and awareness. HCAA is backing the policy shift from testing
on a risk factor basis, to encouraging everyone to get tested, at least once. More and more studies are showing that
targeted testing is missing too many people for elimination of the virus to be realistic by the World Health
Organisation target of 2030. New Zealand has about 30,000 people undiagnosed, and likely to be unaware that health
problems they are experiencing are hep C related.
Hep C Action contributor Dr James Freeman has cured thousands of HCV patients worldwide. He explains why screening
everyone is a good idea for patients and our health system:
“Hep C has quite a lot of symptoms, but they appear slowly and can often be put down to other things like “getting old”
- here are a few of the symptoms:
• Nausea, abdominal pains, weight loss
• Fatigue, brain fog, cognitive difficulties
• Skin irritations, rashes, itching
• Joint pains, headaches”
The global infection rate is about 1%. This a treatable disease can cut 5+ years off the average patient’s lifetime in
addition to the reduced quality of life for many years before that.
Here are some recent articles that suggest one-time population testing is cost-effective in health economics terms:
For individuals, there is a lot of logic in getting screened one time. If you have the disease, get treated, if not stop
worrying. It’s not a lot different to screening for breast cancer, cervical cancer, bowel cancer, prostate cancer, skin
cancer, etc. Most people that get screened don’t have a problem. Some do, and by finding the problem early you can often
fix it and prevent the long-term consequences”.
Hep C Action is calling for elimination by 2025, ahead of the international target.
“We are a small country and have the flexibility to do this the smart way. Let’s get on with it. Ask your doctor for a
test”, says HCAA advocate and survivor Hazel Heal.
“I have seen so many people who have no idea how they got it, had no risk factors. They may not find out until they are
seriously ill”