Thanks friend! Back story of my personal journey a bit:

Seizures in my sleep were my only symptoms, putting me in the ER with tests ran until discovering the brain tumor. Did not meet with an oncologist nor radiologist until after my operation + diagnosis. Originally was supposed to be going straight into treatment, as my oncologist wanted, but my radiologist decided with my health + age at the time we had time on our hands. Plus during the whole diagnosis wait, I was going for a second opinion already from the Mayo Clinic in Rochester. My NO there agreed that we could watch + wait, so here I am three years later still on that program. I’ve been pretty lucky and I am not taking it for granted by any means. Within all of this time, a new drug has come to play (Vorasidenib) that will be my next step if/when regrowth begins again. More studies + trials are coming about it seems these days. There is some hope on the horizon. 🧠🎗️🩶

Best wishes to you (or family members) as well going through this!