i was just recently asked by our neuro and cranio docs to join them to speak about craniosynostosis and specifically chase's journey on the local news station. i am very anxious to be a part of spreading awareness but i feel like we were just diagnosed a couple of weeks ago and may not say what a parent who has already been through the surgery would. if you have any advice or maybe something specific that you might want to be heard please let me know



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born 2.7.10
