this page is for those who have been diagnosed with a meningioma, in particular a petroclival meningioma or more broadly any meningioma occurring in the skull base.
my decision making process - and to an extent my coping mechanism - relies on having all the facts in front of me, which means i've researched the hell out of my meningioma. to me, ignorance is not bliss. ignorance breeds fear. and as such, i strive to be well informed.
hopefully all of the research i've collected over the course of my meningioma journey can help you or an affected loved one navigate this uncertain terrain.
disclaimer: i am not a medical professional, just a layperson patient who has done extensive research for my own health and am relaying my understanding of what i've learned. please do not rely on any of this as medical advice and definitely speak with a doctor for treatment.