I saw the NU doctor this morning. We were there for what seemed like FOREVER! He said it definitely looks like a meningioma, and wants me to send the CTA to him as well. I am to get another MRI and return for a follow up in 6 months. He said that it is likely calcified (the CTA will show that more thoroughly) and that means it may not grow anymore. He also confirmed that it is not causing my dizziness.
He gave me the name of another doctor, whom he called a "dizziness guru." So I will try to get an appointment with him. I told him that the neurologist I was seeing suggested an epilepsy doctor. He seemed to think this was not necessary. So now we have a new direction to go in. No real answers, but the prospects are a little less scary.
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