Deborah’s story: “I’m more determined than ever”
Deborah was diagnosed with liver disease in hospital at 36 years old, just a few weeks after she …
Jenny’s story: “My daughter has her mummy back”
Jenny was diagnosed with Primary Sclerosing Cholangitis at 29 and went on to have a liver transplant …
Clare’s story: “The doctor thought it was all in my mind”
Clare had a very long journey before she was finally diagnosed with autoimmune hepatitis. She is kindly …
Heidi’s story: “I feel very lucky to be alive”
Heidi is supporting the Sound the Alarm campaign for earlier diagnosis of liver disease. She shares her …
Phil’s story: “I wouldn’t have got through it without the British Liver Trust”
Sadly, Phil passed away in December 2024 and our thoughts are with his friends and family. Phil …
Matt’s story: “It all happened so quickly.”
Matt is supporting the Sound the Alarm campaign for earlier diagnosis of liver disease. He explains why …
Sheona’s story: “She tried to live life to the full”
Sheona (pictured) died with Primary Sclerosing Cholangitis in 2011 aged just 24. Her mother, June, explains why …
Elsbeth’s story: “Without these groups, I wouldn’t feel as ‘good'”
Elsbeth is on the liver transplant waiting list and has been diagnosed with a combination of Primary …
Anna’s story: From transplant patient to clinical researcher
After undergoing a liver transplant herself, Anna built a career in the field of transplantation. She shares …
My mum could have been diagnosed earlier if there was more awareness of NAFLD
Samantha is supporting the Sound the Alarm campaign to improve diagnosis, access to treatment and specialist care for …