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.
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!
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