Lucy’s story: “Without my GP making sure my Autoimmune Hepatitis diagnosis was found at the age of 19 I may not have made it this far”
Lucy feels very strongly about early diagnosis of liver disease and being persistent even when she was …
Samantha’s story: “The GP suggested I was a secret drinker and I still feel very hurt about the stigma I experienced. It will never leave me”
Samantha was deeply upset by the stigma she faced from some members of the medical profession. When …
Justin’s story: “I am so grateful and in absolute awe of the miraculous work the NHS achieved, and how strong and positive my wife has remained throughout the process.”
Justin’s wife Lisa was diagnosed with with primary biliary cholangitis (PBC) in March 2020. Here he shares …
Marian’s story: “I look forward to helping with my new grandson.”
Marian has primary biliary cholangitis (PBC) and non-alcohol related fatty liver disease (NAFLD). Thank you for sharing …
Lisa’s story: “Having a transplant has changed my outlook on life.”
After Lisa was diagnosed with primary biliary cholangitis (PBC), she had a life-saving liver transplant. Thank you …
Diane’s story: “PBC may return. If it does, I know what to expect.”
Diane had Primary Biliary Cholangitis (PBC), a rare autoimmune liver condition. She’s shared her liver transplant story …
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 …
Pamela’s story
On my return from holiday, I had an appointment with my consultant and he sent me for …
Gordon Brown’s Story
In January 2011 I went to the doctors with a chest infection whilst chatting to her I …
Pinny’s story
I went to my GP back in 2000 because I had been suffering with diarrhoea for rather …