What Makes Us Tic
Tourette Syndrome is more than a medical condition—it's a unique journey that shapes lives and perspectives.
What Makes Us Tic offers a comprehensive and accessible guide for anyone affected by TS, whether you're newly diagnosed, a parent, or simply curious.
Explore the neurological foundations of TS, learn how to recognize early signs, and discover practical strategies for managing tics in everyday life.
This book also delves into the emotional impact of TS, offering guidance on building resilience and maintaining mental well-being.
Packed with personal stories, practical advice, and inspiring examples of individuals thriving with TS, What Makes Us Tic is your essential companion for understanding and embracing the complexities of Tourette Syndrome.
This is more than just a guide—it's a resource for empowering your unique journey with TS.
You can be a part of this amazing endeavour, by taking part in the National Survey below.
About The Author
Diagnosed with Tourette Syndrome at just five years old, I have spent my life navigating the ups and downs of this condition. My tics started with shoulder shrugging, head rolling, and rapid eye movements. Tourette’s runs in my family, with my younger brother also affected, though his case is more severe.
My inspiration for writing this book comes from wanting to break down the fear that many newly diagnosed individuals—whether children, teens, or adults—feel. Tourette’s can be confronting at first, but I want to offer stories of success and hope to show that it doesn't have to define your life.
I’m not a neuroscientist, psychologist, or doctor—just someone who has lived with TS for over 30 years. I never let it stop me from pursuing my goals, and even when my tics were at their worst in high school, I was elected School Captain, supported by hundreds of students. Now, I am 38, a father to an amazing 4-year-old son, 17 years into my career, and my journey continues.
My hope is that young readers, parents, families, and teachers will come away with a better understanding of life with Tourette’s and see that it’s just one part of who we are—not the whole story.