Chris’ story: “I felt completely accepted”
Chris used to emotionally detach himself from situations to cope with stares, but being the centre of attention at his wedding has given him newfound confidence.
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.
Chris used to emotionally detach himself from situations to cope with stares, but being the centre of attention at his wedding has given him newfound confidence.
Kaylin shares her hate-related experiences to encourage others to join Changing Faces in challenging unacceptable behaviours.
This Rosacea Awareness Month, skin positivity creator Lex shares the ups and downs of rosacea, and advice for those who have recently been diagnosed.
Avril developed Parry-Romberg’s Syndrome as a child. While she’s faced challenges because of it, she hasn’t let it stop her from achieving great things.
Jeff found blending in difficult after losing his foot, due to a lack of understanding on his part and other’s. Now his colourful prosthetics are his trademark.
Maia is an anti-bullying advocate and social media influencer who is paving the way for change. Today she shares her journey with acne.
As a child, Toni was in and out of hospital because of her visible difference, impacting her confidence. Changing Faces helped her to accept herself.
Stephanie’s son, Roman, has Congenital Melanocytic Nevi (CMN). She is passionate about raising awareness of CMN and increasing representation of ethnic minorities with visible differences.
It took Catherine almost three decades to get the correct diagnosis for her visible difference. Now she campaigns, so others don’t have to go through the same.
Danielle’s son, Malachi, was born with complex health conditions. Today, Danielle reminds people to be respectful and kind before commenting on a child’s visible difference.
When Jess developed alopecia, she found it difficult to imagine a positive future. Thanks to her family and a supportive social media community, things are now looking bright.
Angela developed vitiligo aged 14 and shares the challenges and joys that it’s brought along the way.