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.
Professional rugby player Sophie Bridger shares her experience of growing up with CMN (Congenital Melanocytic Naevus), a rare genetic condition affecting around one in 20,000 people.
Leah has Functional Neurological Disorder, which causes spasms and facial paralysis. People’s assumptions have made her self-conscious, but she’s looking to the future positively.
Vikki took part in a pageant expecting to feel out of place because of her facial difference. Instead she found a supportive and inclusive community of women who accepted her exactly as she is.
Rose has multiple haemangioma and naevus anaemicus birthmarks. While it’s taken time to learn to love herself, she now wants to spread the message to others who may feel “different” that they are beautiful and appreciated for the way they are.
Janelle was diagnosed with Juvenile Dermatomyositis when she was six. The comments she received continue to impact her, but surrounded by support, she’s gone on to live a happy life.
Hayley has neurofibromatosis, which has made life challenging, but support from Changing Faces has helped her look to the future more positively.
After acquiring burns scarring on 50% of her body, Charlotte no longer recognised the person she saw in the mirror. But those scars tell a story of survival.
Dahlia’s daughter was born with Congenital Melanocytic Naevus. By writing a children's book, Dahlia is helping to raise awareness and representation for all children living with a visible difference.
Bianca shares her journey to confidence with keloid scarring, finding support in online communities.
Abi was born with Lymphatic Malformation. People’s reactions to her condition made her self-consciousness, but thanks to a strong support network, she’s coming to terms with her condition.
Caroline chose to have a mastectomy after discovering she carries a BRCA2 mutation. Online dating has brought people’s ignorance to light, but she doesn't regret her decision.
Being diagnosed with linear scleroderma was physically and mentally challenging for Holly. Working in medicine is her dream, and she hopes to help others like her feel supported.