The author gives an anecdotal account of his life with developmental prosopagnosia (DP). He was not formally diagnosed until the age of 53 and has evolved a complicated strategy for recognizing people based on non-facial physical features and context. He describes his experiences through infancy, school, university life and courtship, work and family life. He believes that he has lived a full and successful life despite DP but that some aspects of his social and work life were impaired by face-blindness. In his experience people react positively and helpfully if the consequences of DP are explained to them, and this improves social interactions and communications.