Supporting families, promoting research, building community
The George Pantziarka TP53 Trust is the UK’s only charity dedicated to supporting families with Li Fraumeni Syndrome and related conditions. We can make a difference – with your support.
Welcome.
We offer practical support and advice, publishes information for patients and doctors alike and is dedicated to making a difference with research.
Where most research is devoted to understanding the disease, the Trust is aiming to move forward with research on how to reduce the massive cancer risks that blight the lives of LFS families.
We can make a difference, with your support.
Recent years have seen the work of The George Pantziarka TP53 Trust expand. In the next phase of our development we will continue to support individuals and families with LFS. Your kind donations will aid us in the fight.
How will we make the most out of your donation?
Featured
George Pantziarka’s Story
Our charity is named in honour of George Pantziarka, who sadly passed away in 2011. In his short life George suffered three different cancers…
Interview with Min Lu
Professor Min Lu is researching how the anticancer drug Arsenic Trioxide can reshape the mutant p53 proteins…
Introduction to LFS Leaflet
New to LFS? Need to let other people know what it means? Our ‘What is LFS?’ leaflet is designed to be a fast introduction with all the core…