Lottie’s story: “I’ve not let things stop me doing what I love”
Lottie writes about how people's reactions to her visible difference don't stop her from going after what she wants in life.
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.
Lottie writes about how people's reactions to her visible difference don't stop her from going after what she wants in life.
Visible difference champion Ella, who has cranio-fronto-nasal dysplasia affecting the face and skull, prepares for a half marathon.
Mikaela is 28 and has a genetic disorder called Crouzon syndrome. She sees her visible difference as a positive.
Ariel, an inspirational young writer from the US who has Crouzon syndrome, shares how she came to realise that beauty is subjective.