I took this photo and wrote the following in May of 2019, on my 10 year anniversary of moving home to San Diego from Australia. As
by Andi Last, Living LFS Secretary – I am part of a group of people with a rare genetic condition called Li-Fraumeni Syndrome (LFS). You’ve
So a big event is coming up that you really want to attend, maybe it’s in another state or another country, and your bank account
Our private Living LFS Li-Fraumeni Syndrome Support Group continues to grow! For a syndrome that is constantly said to be so rare we are up
by Andi Last – Sean Hannity and Hercules have made Travis Tritt the first person to ever say the words “Li-Fraumeni Syndrome” in a major
