Rather than clinical guidelines, these are personal recollections meant to spark reflection, discussion, and empathy. They emphasize the importance of patient- and family-centered care, the role of storytelling in medical education, and the value of lived experience alongside professional expertise. From navigating diagnoses to balancing autonomy and protection, the narratives underscore the emotional and societal dimensions of childhood-onset disabilities.
The book supports professional learning for clinicians working with children with neurodevelopmental disabilities; strengthens team communication, and offers validation and insight for families navigating similar experiences.
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