Hey JoJo,
I’m glad you atleast have a little more information now! I suggest checking this page out to help with coming up with a list of questions for when you next see a specialist to get more information:
I suggest joining the frontal lobe group: AVM Survivors Network so that when people check out your post they will know your talking about a frontal lobe AVM.
Since it was 10 years ago since you got your diagnosis, understanding of AVMs and treatment technique+technology has developed alot since then. My Neuro-radiologist said the technology he used to treat me would not have been available a few years ago! So there may well be a differant opinion on potential treatment options than you got when you were diagnosed.
Big hugs,
Corrine