Loretta’s story: genomic testing and treatment for Fabry disease

This film series, ‘My genomics journey: three perspectives’, was developed to shine a light on the breadth of experiences of patients living with genomic conditions, and to understand the life-changing impact that a diagnosis can have for a person and their family. In this film, we speak to Loretta who, after having struggled with mysterious symptoms since she was a child, undertook genomic testing and was diagnosed with Fabry disease, an inherited neurological condition. She talks through her experiences of the diagnostic journey, the challenges of living with Fabry disease and the impact that treatment has had on her life.