Living with Vulval Lichen Sclerosss
The experiences shared in this animation were based on the real words of people living with Vulval Lichen Sclerosus (VLS); interviewed as part of the 'Living with Vulval Lichen Sclerosus' study at the University of Bristol and University of Warwick, UK, conducted by Dr Sophie Rees.
We wanted to stir the viewer with almost palpable images, that might cause them to feel an element of discomfort in their own bodies – aiming to invoke a feeling of empathy for the pain, discomfort, shame, loss of sexual pleasure and much more experienced by those living with this condition.
By choosing to depict the vulva in different mediums, and creating six visual metaphors for the experiences shared during the interviews - we were aiming to strike a balance between creating a visceral experience for the viewer and presenting images of the vulva in all of its many, beautiful forms.
The piece is primarily aimed at healthcare professionals, particularly in primary care, to not only improve awareness and increase understanding of VLS and the needs of those living with the condition, but also break down the stigma, and improve education around vulval disorders more widely.
Content warning: depictions of vulva and blood, themes of distress, some viewers with VLS (or without) may find this upsetting.