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 offer practical support and advice, publish information for patients and doctors alike, and are dedicated to making a difference with research.
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…
LFS UK Conferences
Our annual conferences bring together people with Li Fraumeni Syndrome from across the UK and beyond, doctors and researchers. It’s a chance to catch up on the latest from clinical trials, research studies and from each other. The next conference will be taking place on September 12th 2026 in central London…
LFS Information Pack
New to LFS? Need to let other people know what it means? Our Information Pack is designed to be a fast introduction with all the core information in one place.