Teddy The Brave
A children’s book created for craniosynostosis families — helping little ones, siblings and parents feel less alone through diagnosis, surgery and recovery.
Created by a cranio mum
Teddy the Brave was written after our son Teddy was diagnosed with sagittal craniosynostosis and had surgery at 3 months old.
When we were going through diagnosis, surgery and helmet therapy, I wanted something gentle that could help explain the journey to children and make families feel less alone.
This book was created with love for craniosynostosis families — whether you are newly diagnosed, preparing for surgery, supporting a sibling, or looking for a comforting resource to help explain what is happening.
