Last year (my first MRI) showed abnormal signals with expansion in the superior gurus of the left frontal lobe. Suggesting a very-slow growing neoplasm such as a low-grade glioma. I seen a neurosurgeon who said it was benign and suggested that we just watch it. Throughout the last few years I have been suffering from Severe migraines. I have taken different blood-pressure medications, antidepressants, anti-inflammatories, beta blockers, Seizure medications, supplements, pain killers, and receive Botox injections every 3 months ( i am sure i missed something). One of the medications even caused me to lose my short term memory ( i am a full-time student). My migraines will last for months at a time. Over the last year I have been hospitalized on numberous occasions and my sensitivity to smell is far beyond anything you can fathom. Smells now cause and increase the severity of the migraine. I also often suffer from nausea and vomit. My neurologist insists that this thing in my brain has absolutely no relation to the migraines at all. Additionally, I resently had another MRI done and it reads that there has been no substantial change in the T2/flare hyperintence expansion of the superior gyrus of the left frontal lobe, which may reflect cortical dysplasia versus low-grade neoplasm. From what I have read on the cortical dysplasia the majority of people diagnosed are children and suffer from seizures. I am a 30 year old female and have never had a seizure in my life. I am so confused and scared as how to proceed with all this. I feel that they should know what this thing is!!! As I understand it is not aggressive now but does that mean that it will always be like that? I also feel that my neurologist likes to throw medications at me like candy. I seen him today and I got 4 new scripts. One of which is an anti nausea but he gave it to me in a pill form. So if I am nauseous or vomiting a pill is not even going to work. So I don't know what to do. I am so confused.