We need early diagnosis of LFS – not just cancer
Having a mutated TP53 gene wouldn’t be such an issue if there was a way...
Blog
Our aim is to provide practical advice and support, create a sense of community among affected families and to promote research of benefit to people suffering from LFS.
Blog Archieve
Germline p53 isoforms – causing familial cancer?
The first piece of research that we funded was back in 2017, when we funded...
Newsletter #7
Our eighth annual national conference, was held this year on Saturday September 14th at ISH...
Why Is MILI Randomised?
Our charity is named in honour of George Pantziarka, who sadly passed away in 2011....
Newsletter #6
Our eighth annual national conference, was held this year on Saturday September 14th at ISH...
Funding for Whole-body MRI On The Way
A lack of access to the recommended screening, particularly annual whole-body (WBMRI) and brain MRI,...
Newsletter #5
The George Pantziarka TP53 Trust was once again happy to mark LFS Awareness Day by...
LFS Register for the UK
We do not know how many people with Li Fraumeni Syndrome (LFS) there are in...
Newsletter #4
The George Pantziarka TP53 Trust was once again happy to mark LFS Awareness Day by...
Website Survey
We are interested in your feedback on our website - we want to use this...
Liquid Biopsies in LFS – First Results
Early cancer detection is the primary aim in the management of Li Fraumeni Syndrome –...
Online Support Call – Maggie’s Survey
Survey now closed.