Julie on our children and young people’s services during the pandemic
Julie shares resources for anyone with a visible difference during the pandemic, and support for young people returning to school.
Read or listen to real stories from people affected by visible difference, their parents and families, as well as Changing Faces staff and volunteers. Inspired to share your story? We’d love to hear it – share your story now.
Julie shares resources for anyone with a visible difference during the pandemic, and support for young people returning to school.
Lindsay’s dad has a vascular anomaly. Together they campaign for Changing Faces and raise awareness of visible differences.
Robin writes about his daughter's role in Malory Towers and his pride that she's a role model for others with visible differences.
Marie-Joelle’s son Benjamin was born with Goldenhar syndrome. She shares advice for other parents of kids with visible differences.
Rachel, whose baby daughter Freya has a birthmark on her cheek, believes passionately in raising awareness of visible difference.
Eden was born with a lymphatic malformation. Her mum Chelsea now advocates for tackling the stigma of visible difference.
Kimberley writes about her eight-year-old son Charlie, who has raised thousands for Changing Faces and was awarded a young heroes medal.
Inclusive Minds ambassador Hilary writes about parenting a child with visible difference, and why diversity in books is so important.
Sam is a Changing Faces champion who has a cleft lip and palate. He and his mum Claire explain how they cope with people's reactions.