Let's Talk Vitiligo
Everybody is perfect in their own way.
CONTENT WARNING: Contains discussion of suicidal feelings.
#LetsTalkVitiligo is a campaign hero film was created to mark the publishing of the largest ever UK survey of people with vitiligo. Unscripted to-camera interviews and contributor archival stills bring light to what it's like to grow up and live with the condition.
The study revealed the scale of mental health distress among almost two-thirds of people (63%) diagnosed with the skin condition. 8 in 10 people said vitiligo negatively impacts their appearance, and almost half (46%) felt isolated and depressed.
The campaign by the The Vitiligo Society aims to urgently address the lack of awareness and understanding among healthcare professionals and the public. The independent study, commissioned by the UK charity, found that just 15% of those diagnosed felt informed about vitiligo, with a third of people felt dismissed and confused when first speaking to their GP or healthcare professional.
Launched in March 2024, the campaign has featured on BBC & Sky TV and various news outlets.
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The second part of the project delves into more personal stories.
Prod. Co: The Filmworkers
Client: The Vitiligo Society
⭐ Finalist at the Smiley Charity Film Awards 2025.
Director/Producer: Dominic Santana
DOP: James Vivian
DOP: James Vivian
Edit & Grade: Vasil Dzhagalov
Thanks to our brilliant contributors: Natalie Ambersley, Shankar Jalota, Nirjeet Singh Gorvara, Gurdeep Romanay, Dale
Amanda & Izzy
When Izzy was first diagnosed with vitiligo, there were more questions than answers for both mother and daughter — whether to pursue treatment or focus on helping Izzy embrace her ever-changing appearance with confidence and pride.
Angela
When Angela was first diagnosed with vitiligo, she felt like a burden. Then one moment — stepping into a space where she was seen, understood, and not alone — transformed her perspective.
Joti
Joti’s story is one of isolation, resilience, and rediscovery. It wasn’t until she became a mother that something shifted.
Shahn
Shahn was just 7 years old when he was diagnosed with vitiligo — and it broke him. Now Shahn speaks openly about the importance of support, and how the only way to truly live with vitiligo is not to face it alone.
Krystal
For years, Krystal believed the only way to live with vitiligo was to hide it. A change began when she started reading other people’s stories.