Emily Owen grew up in Leicester. Aged 16, she was diagnosed with a rare neurological condition, neurofibromatosis type 2, which has led to numerous operations and left her deaf. Emily speaks at meetings and events, both Christian and secular, and enjoys sharing her life experiences. She is also a trustee of the Neuro Foundation which supports those living with neurofibromatosis.

Emily Owen grew up in Leicester. Aged 16, she was diagnosed with a rare neurological condition, neurofibromatosis type 2, which has led to numerous operations and left her deaf. Emily speaks at meetings and events, both Christian and secular, and enjoys sharing her life experiences. She is also a trustee of the Neuro Foundation which supports those living with neurofibromatosis.

Emily Owen grew up in Leicester. Aged 16, she was diagnosed with a rare neurological condition, neurofibromatosis type 2, which has led to numerous operations and left her deaf. Emily speaks at meetings and events, both Christian and secular, and enjoys sharing her life experiences. She is also a trustee of the Neuro Foundation which supports those living with neurofibromatosis.