Newsletter #4
The George Pantziarka TP53 Trust was once again happy to mark LFS Awareness Day by...
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
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.
Newsletter #3
Molly McQueen, with her mum Katie, organised a spectacular charity ball in Kilmarnock, Scotland to...
Newsletter #2
As we kick off this quarter's newsletter, there's really only one place we can start.
SPAGN – Joining Sarcoma Patients Globally
Sarcomas are some of the ‘core’ cancers associated with Li Fraumeni Syndrome
Newsletter #1
The long-awaited MILI (Metformin In Li Fraumeni Syndrome) trial is almost ready to start recruiting!
SIGNIFIED
As has been repeatedly shown in studies, including the UK SIGNIFY study in 2017
ON-HOLD – New Update Due Soon!
LiFTS: Li Fraumeni over Time Study – tracking changes in LFS over time
FOSTERing change in Osteosarcoma
Osteosarcoma is the most common of the bone cancers affecting children and adolescents
MILI Trial – Funding Approved!
Our charity is named in honour of George Pantziarka, who sadly passed away in 2011....