What does quality advocacy in services aim to maximize?

Quality advocacy in services aims to maximize the participation of service users and their carers. This focus is grounded in the belief that individuals who are receiving services, as well as their families, should have an active role in shaping those services to better meet their needs. When service users and their carers are engaged in the advocacy process, it promotes a more personalized approach, ensuring that their voices are heard and that their preferences, experiences, and insights are incorporated.

This active participation leads to improved satisfaction with services, better outcomes, and more effective support that truly addresses the unique challenges faced by individuals with autism and their families. Advocacy that centers around the participation of service users contributes to a culture of respect, empowerment, and mutual support, which is essential for effective service delivery.

The other options, while they may address certain aspects of service delivery, do not capture the essence of quality advocacy in the same way. Prioritizing efficiency or cost reduction, for example, may overlook the importance of user involvement and may lead to services that do not fully address the users' needs or preferences.