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
I have many phrases that I use to keep myself emotionally grounded. Some of these are not likely to be statements that others would find helpful: “It is
by Ann Ramer I had the opportunity to visit with Dr. Mark Robson this week when I travelled to NYC to follow up with my
I am fairly new to LFS, by many peoples standards, only learning of my family’s genetic problem in 2011. We all understand that this knowledge is life
LFS is hard to explain to the average person out there, who simply cannot fathom the things that we face and are required to consider
I was doing some work on my computer on Thursday evening when the notification on Facebook got my attention. I checked in, and saw some
It is difficult for most people to imagine what it is like when your child has cancer. I have tried to explain what my son
