It is difficult to imagine anything good coming from being diagnosed with Li-Fraumeni Syndrome. Yet as our members remind us, the good is in what
Living LFS means extra scans. Preventative scans. Screening Scans. Treatment Scans. Follow-up scans. Annual Scans. Quarterly scans. This is after an undue amount of time
[pdf-embedder url=”https://livinglfs.org//wp-content/uploads/2016/01/LFS-Final-Project-Jennifer-Mallory-copy.pdf”] A few months ago, I had the opportunity to take an online course entitled Introduction to the Science of Cancer offered by the
The LFS community is extremely rare. We have a rare hereditary cancer syndrome with increased risk of all kinds of rare cancers. In our support
A year ago, a group of ladies who became friends in a support group for LFS met up to talk about what we could do
Lisanne’s grandfather, three of her aunts, an uncle and a nephew – all of them died from cancer. Her daughter got a brain tumour at
Surviving Childhood Cancer can leave quite an impact. Not only are there long term health effects from intense treatments, there are often emotional scars left.
Brian Ries- No Matter the Odds, Keep Fighting. About a month ago, I reached out to the support group to see if anyone was willing
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