Now you can help support us as we support those Living LFS through Amazon Smile. By choosing Living LFS, Amazon Smile will donate a portion
I had the good fortune of attending the Wyss Family Hereditary Brain Tumor Symposium in Columbus hosted by Nationwide Children’s Hospital. While most people would
Rare Diseases Day started several years ago as an awareness campaign built on the idea that there is strength in numbers. There is power in
At 6pm on Friday, October 17th, 2014, mutants gathered in the Pine Room at the Embassy Suites in Portland, Oregon. As they munched on
Exciting things are happening at Living LFS! We have officially incorporated as an organization and are working towards filing for non profit status. As our
Elephants are known for their great size, their tough skin and their impressive memory. They are social creatures where multiple family units come together to
About LFS Printable pdf MDANDERSON LFS Printable Genetics Home Reference NIH American Society of Clinical Oncology(ASCO) LFS Printable .
There are so many symptoms that could be anything, a bug, a bacteria, allergies, or a brewing cancer. Headaches, a cough, lumps, fatigue could all
When you are living with LFS, there are a lot of positives and negatives. Almost everyone is positive that they don’t want to be positive-
On the evening of October 25th, over 100 family members who live with LFS met to share stories and relate to this tough journey over
