Moebius Voices Publishing

Moebius Voices Publishing is an independent publishing initiative dedicated to documenting the history, medical understanding, and community experiences connected to Moebius syndrome.
The titles below explore different aspects of the condition, from medical history to personal experiences and awareness campaigns.
Books on Moebius Syndrome
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Moebius Syndrome: A History of a Rare Condition
Author: Tim Smith
Moebius syndrome has been recognized for more than a century — yet its history is rarely explored.
Moebius Syndrome: A History of a Rare Condition traces the medical evolution of this congenital neurological disorder from early clinical observation to modern imaging and developmental research. Over time, physicians moved from scattered case descriptions to a structured understanding rooted in brainstem anatomy and diagnostic clarity.
This book follows that progression.
It examines how nineteenth-century clinicians first described congenital facial paralysis, how Paul Julius Möbius localized the deficit, how twentieth-century debates refined classification, and how advances in embryology, imaging, and genetics clarified the condition without overturning its core definition.

Moebius Syndrome Awareness Day: A Volunteer-Led Journey to Global Recognition
Author: Tim Smith
Moebius Syndrome Awareness Day began as a simple idea in 2010 and steadily grew into an annual effort recognized across many countries. This book documents that development, tracing MSAD from its earliest planning stages through years of growing visibility and participation.
Written by Tim Smith, founder of Many Faces of Moebius Syndrome (MFOMS), the book presents a clear historical record of the milestones, media mentions, community involvement, and global expansion that shaped MSAD between 2011 and 2025.
Inside this book, readers will discover:
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How MSAD began and the individuals who helped launch it
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A verified year-by-year account of MSAD’s development
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Media coverage and public attention surrounding MSAD
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The growth of global participation over time
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How community-led efforts helped increase awareness
This book serves as a factual, accessible resource for families, advocates, educators, and anyone interested in understanding the origins and growth of Moebius Syndrome Awareness Day.

Voices from the Moebius Community: An Anthology Volume 1
Author: Tim Smith
Voices from the Moebius Community: An Anthology is a collection of personal stories written by individuals with Moebius syndrome and by parents, partners, and family members who walk alongside them.
Moebius syndrome is a rare neurological condition that affects facial movement and expression. But what it changes most often is how people are perceived—and how they are treated—by a world that relies heavily on the face to understand emotion.
The stories in this book are shared in the authors’ own words. They are not edited to fit a single narrative or message. Some are reflective, others direct. Some are written from hospital rooms, classrooms, workplaces, or quiet moments later in life. Together, they show the many ways people grow, adapt, love, and find meaning when expression does not tell the whole story.
This anthology spans childhood, adolescence, adulthood, relationships, and family life. It includes voices from around the world and across generations, offering insight into both the challenges and the ordinary moments that shape real lives.
This book is not meant to explain Moebius syndrome clinically or to offer lessons. It exists to be listened to.
Read straight through or one story at a time. Each stands on its own. Together, they form a broader picture—one built on honesty, trust, and the simple act of being heard.
Available on Amazon (Kindle)
About the Author
Tim Smith is the founder of Many Faces of Moebius Syndrome, an international volunteer community established in 2009. His work focuses on documenting the history of Moebius syndrome, sharing community stories, and expanding public understanding of the condition.
About Moebius Voices Publishing
Moebius Voices Publishing is a small independent imprint focused on books related to Moebius syndrome history, education, and community perspectives. The goal of the project is to preserve knowledge and make reliable information about the condition accessible to families, educators, and readers.
More Titles Coming Soon
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