
ALT "As a mum to a son with the same condition as Jono, I am incredibly thankful and inspired by Jono and what he puts into the world. He was a beacon of hope when my son was born, and has remained so with his optimism, honesty and generosity of spirit. "The world can be quick to judge and we need more people like Jono and the Changing Faces campaigners and ambassadors - individuals who stand up for children like mine, helping to create a kinder, more inclusive world for them to grow up in.”

ALT An orange tile with blue and white brush strokes. At the top is the "CARE" logo and the tagline which reads "Understanding Craniofacial Microsomia". Underneath, the text reads: "Research Opportunity. Were you or a child you care for diagnosed with craniofacial microsomia*? *The CARE study considers craniofacial microsomia to include hemifacial microsomia, Goldenhar syndrome, OAVs and microtia. We want to know how craniofacial microsomia has impact your life! Participation includes completing a one-time online survey. Your answers will be used anonymously to inform future care. Visit www.thecarestudy.org to learn more or scan the QR code below. This study is currently only open to residents of the USA, Canada, UK, New Zealand and Australia. The principal researchers for this study are Dr Carrie Heike at Seattle Children's and Dr Nicola Stock at The University of the West of England, Bristol, UK." Underneath are Seattle Children's and UWE's logos.





























