Help spread the word about Big Yellow Friday 2018
It was fantastic to see so many people joining us on the CLDF Central England Family Weekend
The CLDF community shared their top tips about encouraging their children to take medication
To help raise awareness in Organ Donation Week 2017, Mel kindly shared her daughter Elena's story...
To help raise awareness in Organ Donation Week 2017, John kindly shared his daughter Isabella's story...
To help raise awareness in Organ Donation Week 2017, Emma has shared her transplant story...
To help raise awareness in Organ Donation Week 2017, Abbey kindly shared her son Jack's story...
To help raise awareness in Organ Donation Week 2017, Jane kindly shared her daughter Naomi's story
To help raise awareness in Organ Donation Week 2017, Lisa has shared her transplant story...
To help raise awareness in Organ Donation Week 2017, Kirstin kindly shared her daughter's story
On Saturday 19th August, eight children and their parents headed into the Oxfordshire woods for Wild Camp 2017
Health Visitor Week 2017 is from 21 – 25 August. Mum Charlotte told us about her experience with her new daughter's diagnosis
We had an incredible time at the very first CLDF Weekender!
As we mark World Hepatitis Day this Friday, 20 year old Aidan shares her experience of living with Hepatitis C
For Melissa it was ‘hair today, gone tomorrow’ after she hit her fundraising target!
Later this month we'll be celebrating the British Transplant Games in North Lanarkshire
We want to ensure that CLDF’s health information is accurate; up to date; clear and led by patients and families
Mum Joanne knew that something wasn’t right and followed her instincts to get a diagnosis. Here’s her son Cathan’s story…
Claire has kindly shared her story with CLDF about living with biliary atresia…
Find out what Luke’s up to in his Talk, Tell, Transform film
In our latest blog Dr Jake Mann tells us about a new study which is being planned to look into non-alcoholic fatty liver disease
It was fantastic to see so many people joining us on our Scotland Family Weekend
For International Nurses' Day 2017, Olivia explains how her experiences as a liver patient helped her decide to become a Nurse herself
In her Talk, Tell, Transform film, Daisy tells us what gives her motivation
In her Talk, Tell, Transform 2017 film, Roisin tells us who was there to support her when she needed them
Our next Talk, Tell, Transform film in 2017 comes from Lucy
Here’s Merlee’s Talk, Tell, Transform film as part of our 2017 project
Our next 2017 Talk, Tell, Transform film comes from Aimee
Will’s Talk, Tell, Transform story is inspired by the viewpoint of his parents
Nora shared her story as part of our Talk, Tell, Transform project in 2017
Our next Talk, Tell, Transform film in 2017 comes from Demi
To mark the launch of our 2017 Talk, Tell, Transform films, we're sharing Lucia’s story with you
Oliver took on the Barcelona marathon in March in aid of his cousin Dylan
Jacquie is CLDF’s Families Officer. Here's what she gets up to each day...
We had a fantastic weekend in Northern Ireland with fun activities, good food, and great conversation!
Jade has kindly shared her daughter Lilly’s story to help raise awareness of biliary atresia and encourage parents to be yellow alert.
Mum Sarah has kindly shared her story of daughter Mya, who was born with a choledochal cyst.
One of our young people has kindly shared their choledochal cyst story with us to help raise awareness of the condition
CLDF visited Hertfordshire on Saturday 4th February for a family event at Bedwell Community Centre in Stevenage.
As part of our month raising awareness of choledochal cysts, Leanne has kindly shared her daughter Saffron’s story, who was born with a choledochal cyst and biliary atresia.
“I had never been to a CLDF event and didn’t know what to expect but it was great fun. The best bit was building models out of chocolate and meeting other children who have liver disease like me."
“When I called I felt a surge of relief. I spoke to CLDF’s families officer who was so kind and just listened to our journey.”
“CLDF is so valuable to us because they help you not feel like you're not alone. They understand. They help provide fun when the world doesn't always seem to be that fun.”
“When we Googled biliary atresia, as you naturally do, all the results were from medical journals except for the CLDF page which explained it all in plain English.”
“I met Rich from CLDF. He told me about all the stuff the charity does including Breakaway, a residential trip where I could do a high ropes adventure course and a 24 hour survival course.”
“A lovely lady from CLDF came to see me in hospital. She sat with me while I cried and then told me about the Foundation and how they could help us.”
Childhood liver disease can affect families across the globe. US mum Natalie has shared her daughter Clara’s story with us to help raise awareness of PFIC this month
Mum Gemma kindly shared the story of her son Oliver, who was diagnosed with PFIC as a baby
To help highlight pruritus, one of the common symptoms of childhood liver disease, Rachel has kindly shared her story of her children Wren and Milo
"Having liver disease can be hard, but I want young people and their parents to know that you are able to accomplish great things despite your condition."