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!
Where I am at, in my head
Check out this amazing (noun) who was diagnosed with (part of the body) cancer. They were on (type of treatment) but it didn’t get them down! No way, no how! They are so (adjective) that they signed up for (type of running activity) and completed it. You should be inspired!
Special certificate: brain cancer
A cancer-versary is like an award. I wish I could add "cancer survivor" to my LinkedIn page right after the section about Honors & Awards. Or maybe I can add it to the section about special certificates?
Redefining the support group: my TEDx talk
Liz Salmi, a patient advocate, talks about her decision to be open and share what it is like to live and blog about living with brain cancer in 2013.
How to participate in the #BTSM tweet chat
#BTSM is a patient-run, Twitter community and is not owned by any organization, nonprofit or otherwise. We are for patients and care partners, by patients and care partners. Use the #BTSM hashtag anytime, and join us for a live Twitter chat on the first Sunday of each month.