Welcome to the forum. The hope is that we can use this site so that people affected by Li Fraumeni or other TP53 condition can get together to share info, support and to raise the profile of LFS. I know that you guys in the US are in the process of starting a Li Fraumeni Association, which is great news which we’ll be watching closely.
In the meantime, please feel free to use the forum to post messages about yourself and what you’re doing.
Pan