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.
This is what cute looks like: engaged with brain cancer
There will be MRIs. There will be more decisions about continued treatment. There will be times I forget. There will be times when I worry.
What is family?
Upon hearing the news and finding out that I had a "mass" in my brain, my best friend called her dad. He was in town the next day--asking the important medical questions, demanding answers, advocating on my behalf (because I was too out of it to know what was going on).
Trying Depakote
All of this is great if the tremors go away, but I have been on the new drug for a week and I still have tremors--and they are weird. It almost feels like I've had way too much caffeine and I am shaking with excitement, but I am not excited, nor do I have extra energy.
Mark Miller
There's this guy I met at the UC Davis brain tumor support group, Mark Miller. He was there to make a presentation on managing health with technology – and Mark had brain cancer too.
Taking a break from temozolomide
I am fortunate to be in a position to take a break. I don't remember what a normal body feels like. I know everyone is tired after a day of work, but it is serious work to stay motivated to go on a walk. (Brett keeps me motivated.)
MRI looming and I’m just happy to be alive
At work today I ran into a woman I rarely see around the building. She said, "How are you liking it here?" And I said, "It's great!" And she said, "Well, you sound happy!" And out of nowhere I blurted, "I'm just happy to be alive!"
Sunshine and rainbows
Seriously, I am seeing things in a new light. Maybe the "I am just lucky to be alive" bug got to me.
New regime for anti-seizure medication
What would you rather: Have out of body experiences due to seizures, or have out of body experiences due to your seizure medication? I just can't really tell the difference some times.