My daughter will be returning to the NS after 12 months of wait and see. I am guessing he'll say the same thing as before though: surgery may or may not help. She did not have a syrnix in the last MRI he ordered nor does she show any neurological issues at all. Just 24/7 headache torture. So, I am guessing the CSF MRI is different than a regular one? Thinking I should ask for it. Also, what's CINE MRI? Is it called "sinny" or "sin"? Should I ask for that too? She is seeing Ellenbogan again in Seattle.
Her CM is 11 mm and no other treatment has helped in the least. She's tried so much...we even had her braces taken off to see if that helped (although they'd been on a year before this started). She'd so love to be better.
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