The period of life between 16 and 25 years of age is an important time of change and development, with many young people leaving home, moving into tertiary education, establishing careers, or beginning families of their own. In Australia, more than 8000 young adults are living with a hearing loss requiring hearing rehabilitation. These hearing losses have the potential to have significant and far-reaching consequences for the social, emotional, educational, and vocational lives of these young adults, and it is currently unclear what these effects might be, or whether hearing rehabilitation is reducing them. In addition, while it is known that the effects of chronic health conditions including hearing loss can be effectively reduced by the application of patient-and family-centred care (PFCC), it is not currently clear what constitutes PFCC in this population. This thesis aimed to explore the lived experiences of young adults with hearing loss and to identify the nature of high-quality PFCC among them and their family members. Beginning with two systematic reviews of previously-published research addressing PFCC among young adults with other chronic health conditions, the likely primary elements of PFCC were identified, as well as evidence suggesting that attempts to implement these elements are likely to result in improved outcomes for young adults with chronic health conditions. Following this preparatory work, a survey was conducted to explore the demographics of young adults with hearing loss in Australia, and compare these to those of other young adults in Australia. Significantly poorer life satisfaction outcomes were found for young adults with hearing loss, although a correlation between life satisfaction and the patientcentredness of hearing (re)habilitation was identified, supporting the importance of patientcentred intervention in this population.