Prisha’s story: ‘People with a visible difference can do anything they want’
Prisha is a Changing Faces campaigner and has a rare neurological condition called Sturge-Weber syndrome, which is associated with a port wine... Read More
Working to end visible hate
Our head of campaigns and communications, Gill, shares an update on what’s been happening with our Visible Hate campaign. Sharing experiences Over... Read More
Paulette’s story: ‘Always remember to celebrate our differences’
Paulette is a Changing Faces campaigner and has a birthmark on the left side of her neck. Throughout my life, I have... Read More
Shannon’s story: ‘You will go out there and show them’
Shannon is a Changing Faces campaigner and has a birthmark on the right side of her face. Accepting my birthmark and learning... Read More
Peter’s story: ‘I knew it was ok to be different’
Peter has Sturge-Weber Syndrome, a rare condition associated with a port wine stain. I want to see more representation of visible differences... Read More
Olu’s story: ‘Find yourself as a person’
Olu was born with a lymphatic malformation in the form of a mass on his face and neck. In your general day-to-day... Read More
Eleanor’s story: ‘I am not bothered by my birthmark’
Hi! I’m Eleanor and I was born with a port wine stain birthmark on the right side of my face. And I... Read More
Vitiligo Awareness Month: Natalie’s story
Since 2011, the vitiligo community has been joining together globally to celebrate Vitiligo Awareness Month which aims to re-emphasise the importance of... Read More
Natalie’s story: ‘Being a campaigner has presented me with so many great opportunities’
I joined Changing Faces as a campaigner in 2018 after being in close contact with the charity for a number of years.... Read More
Ella’s story: ‘Being a campaigner for Changing Faces has given me a new lease of life’
I’ve known about Changing Faces from a young age. When I saw the advert calling for campaigners I jumped at the chance.... Read More