Hi All, I am sorry we meet here because of our circumstances. However, we are obviously here because only we know what it is like knowing there is something interfering with Air Traffic Control! It was several months after my "lesion" was identified and seeing a Consultant, even then I didn't leave feeling reassured.
My Benign Menigioma is sitting on top of my brain stem, pressing into the "Pons" area; because of this they strongly advise against surgery. (To quote my consultant's team member, "We are talking feeding tubes ect".) Right?! For that reason, I support that advice. The next step is to monitor it's growth, currently 1.6mm/1.4mm/1.6mm.
I appreciate this is reasonably small and benign, that being a relief as I had Melanoma 10 years previously. He sugested instead of yearly scans, he would like 6 monthly at this stage just to be certain. I was also told that radio therapy isn't an option, due to the location. A bioposy is also not on the cards... all because of it's location. If they are going in, they're going in to remove it.
SO, SO many positives, and I am truly grateful; yet PETRIFIED! I am alone, I have no one to talk to about this without dragging all my other ailments in. I am really scared, it is the elephant in the room. I need to talk about my Menigioma, and I need to know stuff.
🖤