We heard from the doctor's office today. They said that the MRI on Monday just confirmed that Cade has the Arnold Chiari Malformation. We should hear something tomorrow about when we will be able to get in to see the Neurosurgeon. So we pretty much just have to wait and see when we can get into to see him. I was telling my friend today that this is really the worst part. Knowing your child has something and not being able to talk to the doctor who will be treating him.
Thanks everyone again for the prayers and encouragement. We will keep you updated on whatever we here!
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