We are here!

We’re at just over two years out. It seems like glioblastomas (GBMs) are everywhere now. From McCain to more recently a friend of a friend and a coworker’s mom. From us starting our story by searching for survivors, Tom’s story is now what other people need to hold onto hope when given this devastating diagnosis. We’re not in the clear, we never are with a GBM, but he’s beat the median and that’s something. Is it genetics? Diet? Attitude? Science doesn’t know yet. What we do know is we are here to support ANYONE going through this. I hope they know they can reach out to us for advice or just moral support. Please feel free to give our info out if you know someone going through this. A few people talked to us early on and while hard, was a help.

Also coming up-I really hope I can get Tom to post about his diet these days. Spoiler alert-it’s not keto-though we still find value in it for those in early treatment.

Still good!

Sorry for the late post! We had a lot going on before Tom’s last scan. Which turned out to be great!!!! It was not without strife as the MRI machine broke the day before and we had to work with OHSU to get him to another machine and got the results immediately before we left for two weeks to Italy for a friend’s wedding.

We are so incredibly lucky right now but others are not. We hold fast to the one thing we can do which is fundraise to end this. The tumor walk is coming up fast! Please consider walking with us or donating!!!

http://www.braintumorcommunity.org/site/TR/TeamraiserEvents/NorthwestBrainTumorWalk?team_id=82390&pg=team&fr_id=3050