The Liz Army:
A blog
Patient. Patient advocate. Researcher. Student.
There are more than 500 posts here. Use this search to look for something specific. Good luck!
A note about my oldest posts: I began blogging about brain cancer in 2008, at age 29. I had no background or knowledge about healthcare when I started. Please excuse typos and other misconceptions. What you read here is me in real time, like a time capsule.
Erin: founding member
But in the spirit of Erin and her outright frankness, I feel it is my duty to admit that she will be next, in a line of amazing people I've known, to lose their life to a brain tumor.
Talking about median survival time with friends
My friend's reaction reminded me that most people don't know the scope of my diagnosis. I think it is best to keep the details here, on this blog. It is a positive thing for people to be proud of their friend Liz, a "brain cancer survivor."
Changing careers during brain cancer
The one thing truly holding me back was the cost of health care, and worrying about the 90 days it takes to qualify for the new employer's health plan.
Other people's cancer
Sometimes I am so pissed at the world of brain cancer that I look at other cancers like they are inferior and not as crazy or as bad. But that is a bullshit mentality. I look at this girl and all the fucked-up-ness she's endured and realize that all cancers are evil.
National Brain Tumor Society refers patient support to Imerman Angels
National Brain Tumor Society recently sent an announcement that they will be discontinuing their Patient Line and Support Network to instead focus more on research and public policy. While I am bummed about the discontinuation of the patient support network (as I was one of the support peeps) I totally understand the decision made by the NBTS board of directors.
Traveling with brain cancer and epilepsy
When in Rome, take your anti-seizure pills on local time.