Changing Faces

“Since getting support from Changing Faces, I have set myself a goal for 2026 to learn to love my bald self.” After developing alopecia areata, Tracey felt that she’d lost her identity. Following support, she’s on a mission of self-acceptance: social.changingfaces.org.uk/t76NnR

Face Equality Week is just around the corner 💬 This year, our message is simple: Think Before You Speak. Help us create a kinder, more inclusive world for people with a visible difference. Learn more here 👉 social.changingfaces.org.uk/rRCigo

@GoPI3Ks Thanks so much for sharing! 💙

A webinar hosted by Changing Faces: Navigating comments about your visible difference. Wednesday 13th May 6:30pm - 7:30pm. Register here: changingfaces.tfaforms.net/301?utm_source… @FaceEquality

“Don't let other people's comments be the reason you don't achieve what you're capable of.” Rose has multiple haemangioma and naevus anaemicus birthmarks. She wants to show others who may feel “different” that they are appreciated for the way they are: changingfaces.org.uk/story/roses-st…

“I'm still searching for self-acceptance, but I'm getting there as best I can.” Hayley has neurofibromatosis, which has made life challenging, but support from Changing Faces has helped her look to the future more positively: social.changingfaces.org.uk/IdHdkc

“Decades later, the nasty words said to me remain in my mind. Let’s make sure that isn’t the case for others.” Janelle was diagnosed with Juvenile Dermatomyositis when she was six. Today she shares her story: social.changingfaces.org.uk/aRXGhJ

“My scars are proof of everything I’ve survived.” After acquiring burns scarring on 50% of her body, Charlotte no longer recognised the person she saw in the mirror. But those scars tell a story of survival: social.changingfaces.org.uk/eog7xT

“My condition has become a bigger part of my life again, but this time I’m learning how to build a life with it.” Abi was born with lymphatic malformation. People’s reactions made her self-consciousness, but with support, she’s started to find confidence: social.changingfaces.org.uk/TkOmtE

“My scars show that I made empowered decisions that have enabled me to be here for my loved ones.” Caroline chose to have a mastectomy after discovering she carries a BRCA2 mutation: social.changingfaces.org.uk/rM6Rhe

“When people are seen, they begin to heal.” Ash has a condition called Congenital Melanocytic Nevus (CMN). Growing up, she experienced loneliness because of her difference. Now, she dedicates herself to ensuring no child feels alone: social.changingfaces.org.uk/UY3o4a

“Scleroderma affects people in deeply personal and varied ways. I hope to offer support and connection to others in our community.” Holly’s linear scleroderma diagnosis impacted her self esteem and health considerably. Her story: social.changingfaces.org.uk/HyNB0u

“Performing has taught me that everyone deserves to be seen and heard, regardless of appearance or challenges.” Sneha has craniofacial dysplasia, but it hasn’t stopped her pursuing her love of dance, music and teaching: social.changingfaces.org.uk/xJ86gs

“My children gave me a new kind of energy, one that pushes me to walk a little taller, even on days when I still feel that old self-doubt.” Becoming a parent has given Ashleigh, who has NF1, the determination to accept herself: social.changingfaces.org.uk/mbQUPE

“I hope my mental health will keep improving – the support I’ve had with Changing Faces has definitely been a step in the right direction.” Chloe was born with facial palsy. Bullying caused her confidence to drop, but the right support has helped: social.changingfaces.org.uk/1VvYs9

“Hiding a visible difference can be exhausting, and I decided I wanted to try and improve my confidence and self-acceptance.” Reaching out to Changing Faces for support has enabled Mary to live without her visible difference always being on her mind: social.changingfaces.org.uk/YmM0Ky

“Being made fun of for how you were born has long term impacts - but each day I try, and trying is what counts.” Being bullied caused Enoch to develop anxiety. Now he uses social media to show that looking different doesn’t mean you need to hide away: social.changingfaces.org.uk/yh77Zg

“I’d love to give back to Changing Faces, because knowing there’s support available is vital in this journey.” Lacey’s mum Sara is running 10k to raise funds for Changing Faces. You can read Lacey’s story and donate here: changingfaces.org.uk/story/lacey-st…

“My Skin Camouflage products enable me to get out and about without having to worry about what people might say to me.” Developing telangiectasias took a toll on Jen’s confidence. Changing Faces' Skin Camouflage service has helped her to build it back: social.changingfaces.org.uk/xcPq3Y

📢 We’re #Hiring! We're looking for a Children and Young People Development Officer to lead and develop a national provision for CYP and their carers affected by visible difference across the UK. Learn more: social.changingfaces.org.uk/KEfGgc

📢 We’re #Hiring! We're looking for an Interim Head of Transformation. This home-based role will focus on increasing the reach and impact of our services across the UK, with lived experience at the heart of decision-making. Apply here, deadline Monday: social.changingfaces.org.uk/QV8g6v