Two doctors said I possibly have a neuroma in the area where the neurosurgeon cut the C2 nerve root. They say it branches out like a tree root in my head but there is no test to show this. Crazy huh? MRI of C spine did not show it nor did CT scan of head. I really would like another MRI of my brain but cannot get one. Also having facial spasms and eye spasms and deep nerve pain in both ears. I am so scared. Anyway for fibro I learned from my fibro friends that it is important to take the magnesium separate from the calcium as the calcium builds up, does not bind with the magnesium, thus my bone spurs. Also I have big knuckles, another sign of calcium buildup in fibro and scaly scalp. We supposedly have too much phosphate in our body, thus a lot of fibros take the guiafenesin which releases it from our bodies. This excess phosphate causes the muscle spasms. Dr. St. Amand's book explains all of this. It can even cause spinal stenosis. We all need more magnesium, even as much as 2500 mg a day and to get our levels tested. Anyway enough said. I hope we all get better with something. I know I cannot go on like this.