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 …
Danielle’s story: “If I’d had better care right from the start, the liver damage might not have progressed so far”
Danielle, from Glasgow, has auto-immune hepatitis (AIH). She’s supporting our campaign to sound the alarm on liver …
Eleanor’s story: “I’m thankful for time we didn’t expect to have.”
Eleanor is supporting the Sound the Alarm campaign to end late diagnosis of liver disease and liver …
Craig’s story: “It’s hard to compare the recovery process when you live alone to having a partner there for you”
Craig had a liver transplant after being diagnosed with alcohol-related liver disease. He shares his thoughts about …
Sharan’s story: “Dad’s passing has left a huge void in our family”
Sharan’s father (pictured) was diagnosed with non-alcohol related fatty liver disease (NAFLD) in 2004. Since his death, …
John’s story: “My life before and after transplant is like night and day.”
John didn’t realise he had a liver condition until he was taken to hospital after a hypoglycaemic …
John’s story: I’m still very active
John was diagnosed with Primary Sclerosing Cholangitis (PSC) in 1994 and had a liver transplant in 2002. …