Emma TreleavenEmma and Samuel Treleaven are from the country town Kalgoorlie and are the parents of little Savannah. At just 5 days old, Savannah was diagnosed with persistent fetal vasculature (PFV) and a congenital cataract. Whilst trying to ease their nerves ofsurgery day, they sat together in the hospital and was inspired to write this story. They hope that this story brings awareness towards PFV and allows other patching children to wear their patch with bravery and confidence, with a chronicle of Savannah's journey that they can look back on for years to come.Thank you for being a part of Savannah's journey. Read More Read Less