In December of 2016, while I was working as a postdoc in Canada, I started having horrible headaches that I assumed were caused by migraines, along with dizziness and nausea when I was more active. After two weeks, I went to the emergency room and got a CAT scan that confirmed I had two tumors in my brain. It was shocking, and I knew very little about brain tumors.
After my first surgery, I was told the surgeons removed a glioblastoma tumor with an IDH-1 mutation. The second surgery came about ten days later, and a grade-3 astrocytoma was removed. I was supposed to start a tenure-track job at a university in Boston in January 2017, but this was impossible as I was better off in Canada for my first round of brain cancer treatment.
I was tumor-free for the next 6 years until I learned that I had a fast-growing meningioma in May 2023. It grew so aggressively that the radiation treatment my oncologist planned for me was no longer an option, and I needed surgery on November 1, 2023. Luckily, this third surgery was “easier,” but I required a lot of help with daily tasks for about eight weeks. Cut to April, and the meningioma is recurrent. The news is demoralizing, but my team is on a fast treatment path, which will include stereotactic radiography surgery.
I have dedicated my time to advocating for more research on brain tumors and research funding for other cancers that I have seen loved ones suffer through. While my life with brain cancer and caring for myself is often challenging and time-consuming, I feel lucky that the disease isn’t worse. I can live my life and enjoy most of my time. While these tumors keep knocking me, I will not go down. I am still around and will use the rest of my time here to uplift others.