She has no care in the world and no idea of what is to come and for that I am grateful. If this had to happen, I am so thankful it's when she is too young to remember it one day (I hope).
When she was first diagnosed with Craniosynostosis, I thought why my baby. I asked that once and never again. There really is no answer why and dwelling on it won't change it. I do know that if there has to be anything, I am grateful it is "just" this. Something that surgery can correct and I thank GOD we have a Pediatrician, Neurosurgeon and Craniofacial Surgeon that have expertise in the subject.
Once you've spent time in a Pediatric Neurosurgeon's waiting room or a Children's Hospital for that matter, you definitely realize your priorities and acknowledge your blessings if you hadn't already done so before.
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