Rebecca
Rebecca developed acne at the age of 12/13. She began picking at her spots and this developed into a condition called dermatillomania. Her acne cleared up with a GP prescribed cream to dry out the spots, but she continues to have dermatillomania.
Rebecca developed acne at the age of 12/13. Not many of her peers had acne then and she felt very self-conscious, although her parents reassured her that most teenagers get some spots. Rebecca began picking at her acne which she says developed into a condition called dermatillomania. This is when a person compulsively picks at things which they think of as blemishes on their skin. For Rebecca, it became a cycle when skin picking led to scabs which then became the focus of attention for further picking. Rebecca’s acne is now gone but she continues to have dermatillomania, something which she’s very involved in awareness raising for.
When she first started to develop acne, Rebecca went to the GP with her mum. She was given a cream to use to dry out the spots. However, the cream made her skin extremely dry and went back for a prescribed moisturiser. In an effort to get rid of her blemishes, Rebecca began picking at her skin. Although she had had acne mostly on her face, back and arms she began picking at other parts of her body too, such as her legs. She would pick at her skin, sometimes several times a day, as a response to feeling anxious about her appearance. Rebecca realised it was a problem when she found that she couldn’t stop and she would wake up to find blood on her bedding. Rebecca looked online about her behaviour and learnt about dermatillomania. She went to her GP for help but feels that the doctor didn’t understand. She was referred to her local Children and Adolescents Mental Health Services (CAMHS) who then suggested she should be treated under dermatology. Rebecca thinks it’s important to emphasise the links between skin and mind involved in the condition, but her experience of medical care did not seem to link these together.
Rebecca struggled a great deal with bullying at school about her acne, scabs from skin picking and because Rebecca was seen to act differently too. She stopped taking PE classes as she felt embarrassed about the other students seeing her skin. She remembers being asked what the marks were and she tried to brush off the questions. Rebecca experienced verbal and physical bullying at her school, and ended up moving schools when she was in Year 9 for a fresh start. Rebecca had a good experience at her new school and, once she knew more about the condition herself, she became more confident explaining about her dermatillomania. Although she still feels self-conscious sometimes, preferring to wear make-up and long sleeved shirts, Rebecca’s becoming more confident. For example, she recently wore a swimming costume on holiday something which she had avoided doing for many years because of her scars.
Rebecca continued researching online about dermatillomania and looked for a charity or support group based in the UK. Unable to find one, Rebecca decided to set up her own webpage for sharing experiences and giving support. She finds that most people haven’t heard of the condition before. In her experience, this includes medical professionals and she’s set up a campaign to include dermatillomania in medical training.