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, Advocacy Liz Salmi Surviving, Advocacy Liz Salmi

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.

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Surviving Liz Salmi Surviving Liz Salmi

Creating a positive cancer environment: Stupid Cancer rocks the house

Probably the most amazing moment of all was on the first night I was there. There was a kickoff event in a nightclub for all the young adult cancer survivors and halfway through a beautiful young woman walked up to me and said my name. It took me about five seconds to realize I was looking at Emily, a young brain cancer survivor I met 10 months ago via my blog.

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