
Last year I met with a shaman (side note: it was totes kosher because he was half-Jewish – a Sh’ma’n?). The shaman was awesome, and mostly what you probably imagine a shaman to be: wise, magical, smelling of sage. He…

Last week, I got a message out of the blue from an acquaintance: “Lisa – I just wanted to send you a note of thanks for sharing your experience and being so open. I went to get a chest X-ray…

Five years ago today, I checked into the hospital for an out-patient biopsy that was supposed to be NBD and woke up to the worst news of my life. In general, I don’t mark my “cancerversaries.” I prefer to reserve…

We have a friend that’s super into very challenging wood puzzles. I got curious about her hobby a couple years ago and she sent me a few to try. They were some of her more entry-level puzzles, but I still…

It took me almost a year after the diagnosis to buy anything for myself that wasn’t related to my medical care. In late 2014, finally feeling well enough to enjoy strolling around our local town, I vividly remember wandering into…

I always sigh when fellow LC patients say “it’s been a rough stretch,” like it’s some kind of aberration when our community loses someone special (or a few someone specials in a row). Death is such a constant in the…

I am excited to share the latest news about the ROS1 Cancer Model Project. First, a refresher on the project: The Problem – ROS1+ cancer occurs in many types of cancers, but it is rare. This makes it difficult for…

In 2016, I listened to a podcast about genetics and cancer featuring oncologist Dr. Theo Ross. During the interview Dr. Ross mentioned that if you don’t smoke, you reduce your risk of getting lung cancer by 95-99%. It was a…

Since I’ve been holding steady on my treatment, I haven’t needed access to a clinical trial yet. However, clinical trials may become essential to my survival, and I’m already concerned about getting into them when I need help the most….