CLDF
Cookies Policy

We use cookies on this website to enable you to get the best experience. If you continue without changing your settings, we'll assume that you are happy to receive cookies. To find out more about what we use cookies for, or to find out how to change your settings, please read our cookie policy.

Home Blog

Blog

  • CLDF Weekender 2017
    (08/08/17)
  • World Hepatitis Day 2017
    (26/07/17)
  • To baldly go…!
    (25/07/17)
  • British Transplant Games 2017
    (18/07/17)
  • Producing CLDF Health Information
    (04/07/17)
  • Cathan’s biliary atresia story
    (27/06/17)
(08/08/17)
We had an incredible time at the very first CLDF Weekender!
(26/07/17)
As we mark World Hepatitis Day this Friday, 20 year old Aidan shares her experience of living with Hepatitis C
(25/07/17)
For Melissa it was ‘hair today, gone tomorrow’ after she hit her fundraising target!
(18/07/17)
Later this month we'll be celebrating the British Transplant Games in North Lanarkshire
(04/07/17)
We want to ensure that CLDF’s health information is accurate; up to date; clear and led by patients and families
(27/06/17)
Mum Joanne knew that something wasn’t right and followed her instincts to get a diagnosis. Here’s her son Cathan’s story…