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!

Surviving Liz Salmi Surviving Liz Salmi

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.

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Surviving Liz Salmi Surviving Liz Salmi

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.

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Surviving Liz Salmi Surviving Liz Salmi

The meaning of the cancer tattoo

The octopus in my tattoo represents a combination of things. It is the chemotherapy drug that, once passed through the blood-brain barrier, seeps through my brain tissue, finds the tentacles of my tumor, killing cancerous cells. The octopus can also represent a mental image of a smart creature protecting me from the claws of a crab.

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