Real stories

Paige hopes people can embrace all forms of difference in future, viewing uniqueness as part of everyone’s beauty.

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

Lucy’s eczema has caused her physical and emotional pain, but after receiving support from Changing Faces, she’s rewritten the narrative surrounding her condition.

Dave joined our online group support, Peer Group Chat, because he wanted to connect with people who could relate to having a visible difference.

Rob speaks about the importance of being an ally to people with visible differences, and why empathy is the key to everything.

For the visible difference community, Halloween can be a terrifying reminder of the association between difference and monstrosity. Campaigner Chris believes films aren’t helping.

Dressing up for Halloween is part of the fun, but Sophie is asking people to think about the impact of using a condition as a costume.

Bullying made Lizzy lose her self-confidence, but through challenging herself, she now sees her cleft as a source of strength.

Dean shares his journey with alopecia areata, and why he's trying to break down the stigma surrounding men’s mental health and alopecia.

When Kimberley’s son, Charlie, didn’t get into his choice of secondary school, it was an upsetting time. Today, Kimberley shares how they moved forwards.

After acquiring burns as a child, Tom struggled to find acceptance. Now he puts himself first, surrounding himself with people he loves.

Ellie has faced stares and stigmatic comments due to scars caused by self-harm, but she hasn’t let this stop her from achieving great things.