Child Pain, Migraine, and Invisible Disability

This insightful exploration addresses the often-overlooked needs of children suffering from migraines, as discussed in Child Pain, Migraine, and Invisible Disability.

In the twenty-first century, there is a growing global acknowledgment that pain relief is a fundamental human right. However, in Child Pain, Migraine, and Invisible Disability, Susan Honeyman highlights how this recognition has often been shaped by adult ideological needs, leaving the specific requirements of children in pain marginalized or ignored. This book provides a critical perspective on how societal views have historically sidelined the voices of young patients, emphasizing the need for a more child-centered approach to pain management.

The book delves into the experiences of children suffering from migraines, exploring the profound social and disabling impacts of chronic pain. By utilizing a blend of medical, political, and cultural discourse, Child Pain, Migraine, and Invisible Disability sheds light on the concept of invisible disabilities among children with migraines. Honeyman supports her arguments with authentic accounts from migraine sufferers and first-hand interviews, alongside a rich array of historical, literary, and medical references that have never before been compiled in a child-focused context.

Moreover, the book examines representations of child pain and migraines across literature, art, and popular culture, offering an interdisciplinary framework for understanding these issues. It will resonate with scholars in fields such as childhood studies, disability studies, and medical humanities, as well as anyone who has experienced migraines or cared for children dealing with chronic pain.