Real stories

Oliver Bromley and others in the visible difference community have experienced discrimination in hospitality venues. With allyship and better education, we can put a stop to it.

While it took Gillian 17 years to discover she has Parry-Romberg Syndrome, she has spent that time learning to love the way she stands out.

Kate has had to deal with invalidating and unkind comments because of her microtia. She wants the film industry to improve representation of difference, so others don’t have to face the same ignorance.

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.