Emma Update

Well we heard from the Neurologist and saw our pediatrician and ophthalmologist yesterday. They said that they believe it might be a "Ophthalmoplegic migrane" They can occure often but the more they happen the less likely the eye will fully recover. There isn't any sure treatment to help prevent it from happening again. We are going to have one more MRI done to be sure there is nothing putting pressure on the nerve. We will not be able to see the Neurologist until March or April. Right now we are just waiting and hoping her eye opens quickly. I am glad we finally have a name to put with this problem and that we can know more about it. If you have more questions there is a lot of stuff to read if you google it. That is pretty much what I have been doing and making a list of questions for the Neurologist when I do get in to see him.