Thanks so much every one. I pray she doesn't have this either, but at least she doesn't need to go 3 yrs to find the answer's. I stressed to the tech before they took her in for the test to look for this. Us with Chiairi now all about the Chairi run around. Having gone through it myself. I'll try my hardest that she doesn't have to endure it. She watched me go through all the pain, and now I see it in her eye's. It's said, we will find out and I'll let you know. Thanks again for the prayer's. We all know to well.
Im prayin your daughtet doesnt have chiari. But then the journey would begin lookin for answers to what else th symptoms are from. Wish u both luck :)
P.s. i think of u 2 and hope the best...my twinsister has an endoscopie on a malformation of a vain on her brain...i am so nervous...hope everything will be good for her and ur daughter
Hi...mine was already seen by a ct scan,but mri is the best.hope ur daughter will not have it...good luck