Ashley’s STORY
Ashley has Treacher Collins syndrome meaning he was born without a jaw, cheekbones and ears. Ashley shows us how he gets around the daily challenges that his symptoms present and how he deals with the bullying that he has experienced as a result.
Genetic Disorders UK would like to thank Ashley and his family. We would also like to thank the Treacher Collins Family Support Group which provides support to children and their families living with the condition.