Real stories

Oliver’s story of being refused service at a local eatery shows we’ve still a long way to go in reducing intolerance and promoting equality.

Atholl reflects on his time as a Changing Faces campaigner and how he continues to campaign for the visible difference community today.

Following surgery for a rare bone condition, Ajay was left with ptosis. It’s taken time to accept his new appearance, but he’s not let that hold him back.

Michelle was born with a craniofacial difference, impacting her self-esteem throughout her life. Support from Changing Faces and her family has been vital.

Performing in front of a crowd has enabled Stacey to feel empowered by all eyes being on her. When people stare, she wants it to be because of her talent.

Hannah struggled with her self-confidence until she discovered a love of art – a passion that helped her recognise all the amazing qualities she hadn’t seen before.

Liam has faced stares and bullying because of his condition, but through confidence and creativity, he wants to change the narrative surrounding difference.

Izzy shares her experiences of living with a visible difference in Portugal and the UK, as well as what she gained from our online group support, Peer Group Chat.

Gemma’s son, Finley, has a rare condition known as lymphangioma. She shares her family’s journey and hopes for Finley’s future.

Mikaela shares her experiences of being a part of the Stratford Community Chorus, for the Royal Shakespeare Company's production of Julius Caesar.

Last year, Tee shared his journey towards feeling comfortable with his sexuality and appearance. Today, Tee updates us as a trans man with a visible difference.

Kate's son William was born with the condition Treacher Collins Syndrome. She shares her family's journey and hopes for William's future.