The monthly Hepatitis B Virtual Support Group is a safe and confidential space where you can meet with others in the UK living with Hepatitis B. At the meetings we share reliable information on how to live well with the condition, learn through sharing experiences, and promote patient advocacy to give people affected by Hepatitis B a voice.
Find out more about the group today.
Register hereUnderstanding Hepatitis B
What is hepatitis B?
Hepatitis B, sometimes called hep B or HBV, is a virus that infects the liver. Hepatitis B is the most widespread form of hepatitis worldwide. Most people clear the virus by themselves and it has no lasting effects. But in some people hepatitis B infection becomes long term (chronic). If this happens, it can cause liver disease.
Who is at risk?
Most people living with hepatitis B got the virus when they were born or as a young child. There is more chance of this happening in countries with higher levels of hepatitis B (the UK is not one of them).
The virus is spread through blood and other bodily fluids. This means it can be passed from a mother to her baby. It can also be passed on during sex. Or by sharing any items that can get blood on them, such as razors or needles for injecting medicine or drugs.
Read more about how hepatitis B is passed on.
Vaccination
There is a vaccine for hepatitis B. In the UK babies are vaccinated against hepatitis B at birth, this started in August 2017.
Pregnant women who are at high risk of having hepatitis B can have the vaccine.
Vaccination is also free for anyone who is at risk of hepatitis B. Speak to a doctor about getting the vaccine.
Read more about vaccines against hepatitis B.
Treatment and testing
There is no cure for hepatitis B, but there are treatments available that can manage the condition. Treatment makes you less likely to get serious liver disease. And can also reduce the levels of the virus so that you cannot pass it on. Read more about treatment for hepatitis B.
If you think you could have hepatitis B, you can ask your doctor for a test. Find out more about tests for hepatitis B.
Living with Hepatitis B - personal stories
When Claire was diagnosed with hepatitis B, she found herself facing not only a serious health condition but also a lack of information and understanding. In this video, Claire bravely shares her personal journey from diagnosis to advocacy. She talks about the challenges she faced, the importance of seeking support, and her mission to raise awareness and tackle the stigma surrounding hepatitis B.
Monica’s journey with hepatitis B took a challenging turn when it progressed to liver cancer, eventually leading to a life-saving transplant. Monica shares her powerful story of resilience and recovery. She emphasises the critical importance of regular surveillance for those with hepatitis B to ensure early diagnosis and timely intervention.
Support and information for you
Hepatitis B information
Read more
Our helpline and support groups
Find out moreHepatitis B news and research
Find out more
Living with a liver condition
Read moreMyths vs Truths
We know that there are many myths and incorrect information out there about hepatitis B. The statements below are some of the false claims that we have heard. Click on each one to read the truth.
MYTH: You can't enjoy a meal with friends
TRUTH: You cannot pass on hepatitis B by sharing a meal.
MYTH: You can't hug your loved ones
TRUTH: You can hug your loved ones. Hepatitis B is passed on through blood so hugging does not pass it on.
MYTH: You can't have kids
TRUTH: People living with hepatitis B have children and a normal family life. Vaccination is a safe and effective way to stop the virus being passed on.
MYTH: The spread can't be controlled
TRUTH: Hepatitis B can be treated and controlled.
MYTH: You're on your own
TRUTH: Hepatitis B is one of the most common viral infections in the world, so you are not alone.
MYTH: It's your fault
TRUTH: Hepatitis B is mainly picked up at birth or in childhood. However you got hepatitis B, it isn’t your fault.
Stamp Out Stigma
At the British Liver Trust, we believe that people with hepatitis B deserve support, not judgment. That’s why we launched the Stamp Out Stigma campaign, aiming to:
- Empower those with liver disease to challenge stigma.
- Educate healthcare professionals and the public.
- Raise awareness of stigma’s impact.
Watch Amanda’s story to see her journey from darkness to light and understand why people with hepatitis B should hold their heads high.
Facing Stigma?: Find help and advice here
Join the Campaign: Add your name to Stamp Out StigmaHelp us continue to provide essential resources, support, and advocacy for those affected by hepatitis b.
Your support is crucial in our fight against hepatitis B stigma. Make a difference today.
Donate