Little Léah's story of metopic craniosynostosis, a seen through the eyes of her loving father.
My story started more than a decade ago. This is how I first described the story back then, on the "4 months anniversary of her operation" (I will add the pictures again later. They have disappeared from the forum where I initially gave regular updates on Léahs story. You can go back and read them here. I will put all the pictures here in due course).
Yesterday, it was exactly 4 months since my daughter Léah was rolled into theater