Journey with Genetic Craniosynostosis

Journey with Genetic Craniosynostosis Journey with Genetic Craniosynostosis Journey with Genetic Craniosynostosis
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Journey with Genetic Craniosynostosis

Journey with Genetic Craniosynostosis Journey with Genetic Craniosynostosis Journey with Genetic Craniosynostosis
  • Home
  • About Us
  • Contact Us
  • In memory of Brentley
  • Types of mutations

My why

About Me:

I’m Christina, the founder of Journey with Genetics/ Late onset Craniosynostosis.

I studied at The University of Akron in legal studies, but am currently a stay at home mom to 3 beautiful kiddos. 

When my oldest son Noah was diagnosed with genetic/ Late on set, I was surprised that I couldn’t find much. When I looked up even more genetically it was all terms that I didn’t know. I made this page in hope that if another cranio momma or dad has a child with late or genetic they come to a space that is easy to understand.

Our mission

Raising Awareness

At Journey with Genetic Cranio, we are raising awareness on Late/ Genetic Cranio. 

This page is to help raise awareness and be a safe support system to parents of these amazing kids!

Copyright © 2022 Journey with Genetic Cranio - All Rights Reserved.

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  • Types of mutations

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