Patient & Researcher Blog
Here I aim to capture what I am learning as a newbie researcher from a patient perspective.
Living with a slow growing brain cancer
It is taboo for researchers to talk about their work before it is published.
I think that’s a bummer.
My favorite part about research is learning new things in real time. Here I share my observations as a learner and my n of 1 (personal) findings as a patient.
Note: I started blogging about brain cancer in 2008, at age 29.
I had no background or knowledge about healthcare when I began. Please excuse typos and other misconceptions. What you read here is me in real time, like a time capsule.
There are more than 500 posts here. Use this search to look for something specific. Good luck!
David, Part 1: When your brain tumor friend starts hospice
That was the weirdest fucking goodbye of my entire life.
Seizure drugs: Where is our jetpack?
By the way, no matter who you are, or what you do, someone will always be older than you and will be able to get away with belittling your minor neurological deficits.
Questions submitted for the 2012 National Brain Tumor Society Summit
Before I left for the National Brain Tumor Society's annual summit I asked The Liz Army blog readers if you had questions you would like me to ask doctors and health care professionals I would presumably meet at the event.
My brain: 16 months after Temodar
Hallmark is seriously missing out on the "thank you for saving my life" card genre.
Getting back to exercise after brain cancer treatment
If life is short, and if my tumor grows back, it is worth having made myself as strong as possible before the fight. It is worth feeling good in my own skin, especially if I only have a short time in this skin.
Baseball: the ultimate cancer therapy
Whenever Tim Lincecum struck out a batter, Buster Posey hit a home run, or Pablo Sandoval wore his hat sideways during a rally, I felt like I was part of something greater than myself. I became one of hundreds of thousands of fans in orange and black who leave their hearts in San Francisco.
Lobbying with my emotions: brain tumor advocacy is conjuring up all kinds of dirt
I have no idea if my father is 'proud' of me, but in my mind he has no right to be proud. Because nothing of who I am reflects on him, his skills as a parent or of who he is as a person. Pride is feeling good about something you did. He never did anything, and he certainly never reached out during my entire cancer process. I never got flowers. I never got a card. He didn't come to my wedding.
Brain tumor advocacy in full swing: it's time to educate Congress
There are people who are mortgaging their homes just to get their kids the Temodar they need. Some people are skipping their treatment and using it only every other month.So you can imagine what a blessing it would be to brain cancer patients everywhere if our chemotherapy was treated the same way as chemo for every other cancer patient. For reasons unknown to me, we are being discriminated against, and this is not OK.
MRI one-year post Temodar chemotherapy
Since I am psychic, and have answered a million questions about brain scans, I am going to answer all the questions I know you have.