Deirdre Croft has invested 45 years in caring for her intellectually disabled son, Richard, whose severe brain injury at birth left him non-verbal and dependent on 24/7 care. As she approaches her later years at 72, Deirdre grapples with the distressing reality of what will happen to Richard after her death. Her love for her son drives her to prepare resources, including a video message for Richard, that she hopes will provide him comfort and connection even in her absence.

The challenges that Deirdre faces resonate with thousands of Australian parents in similar situations, highlighting a pressing social issue regarding the care and support of individuals with intellectual disabilities. Many parents worry about the future stability and well-being of their children when they can no longer be around to support them. Deirdre's proactive approach underscores the emotional and practical complexities these families face as they work to ensure a semblance of security for their loved ones.

This story serves as a poignant reminder of the need for societal and governmental support structures that address the long-term care of people with disabilities. Deirdre’s experience points to the broader implications for families, urging a community-wide conversation about sustainable solutions that would help secure the well-being of individuals like Richard, highlighting the crucial role of advocacy and awareness in these discussions.