Helen’s story: “I’ve decided to embrace my differences”
After years of trying to hide her scoliosis, Helen has found the confidence to own her condition and accept herself.
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.
After years of trying to hide her scoliosis, Helen has found the confidence to own her condition and accept herself.
Katie's eczema comes and goes. Sometimes she doesn't know whether it’s coming or going. She says that every day is different and everyone who has eczema shares a different story. Today, Katie shares hers.
Throughout October, our campaigner Peter has been walking an impressive 70 miles to raise money for us. Here’s why he wants to go the distance.
After sustaining scars to his face and body, Joe started to shut himself away to avoid stares and judgement. With help from Changing Faces’ skin camouflage team, he soon felt his confidence grow.
Sudha developed a facial scar as a baby, which impacted her confidence growing up. Now she’s found acceptance.
Lottie has faced a number of mental health challenges – now she wants to help others in the same position.
After using skin camouflage products since she was a child, Felicity decided to become a Skin Camouflage Practitioner - and support others using our service.
It took 30 years for Sean’s condition to be diagnosed, but now he’s on a mission to educate others.
For the first time since acquiring PAH, supermodel Linda Evangelista has got back in front of a camera. Our campaigner, Sophie, shares her thoughts.
Chantel has rosacea, and after lockdown, started to struggle with low self-esteem. Joining our online group support, Peer Group Chat, Chantel was able to meet other people who had shared experiences of living with a visible difference.
Over a year has gone by since Ashleigh acquired her scars. Today, she shares her story to encourage others to seek support and rebuild their life after such a life-changing experience.
Alice and Dan share their experiences of having a 19-month-old daughter, Lily, who has Sturge Weber syndrome.