Tourette Syndrome Essay

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What makes me tic?:
An investigation into the possible causes of Tourette syndrome and its symptoms
Gilles de la Tourette Syndrome, commonly known as “Tourette syndrome,” “Tourette’s,” or simply “TS,” is a chronic neuropsychiatric disorder producing sudden, repetitive movements and sounds, known as “tics,” which are beyond an individual’s control. The condition is named after French physician Georges Gilles de la Tourette, who first published an account of its symptoms in the 1880s (Felling & Singer, 2011, p. 12387). Once considered a rare disorder, Tourette syndrome is currently estimated to occur in mild to severe forms in as much as 2% of the population (Bohlhalter et al., 2006, p. 2029). Today, Tourette syndrome affects the lives of millions of people around the world – including me! What causes this complex disorder and its notorious symptoms?
Diagnosis and symptoms
Tourette syndrome is commonly diagnosed in children following an onset of tics between the ages of 6 and 9 years (Galvez-Jimenez, 2012, p. S35). In many circumstances, Tourette syndrome occurs alongside one or more additional disorders, such as Obsessive-Compulsive Disorder (OCD) and Attention Deficient Hyperactivity Disorder (ADHD). I was diagnosed with both Tourette syndrome and OCD at eight years of age following an explosion of tics, twitches, and obsessive-compulsive behavior. To be formally diagnosed with Tourette syndrome, a patient must be under 18 years old and exhibit multiple motor tics and at least one phonic or “verbal” tic for at least one year (Galvez-Jenez, 2012, p. S35). Tics are sudden, repeated, involuntary body movements or vocal projections that are classified as “phonic” or as “motor.” Motor tics are sudden, impulsive, purposeless body ...

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... severe ear infections, which ultimately required surgery. Given my genetic makeup and early life experiences, it appears my Tourette’s diagnosis was triggered by both hereditary and environmental factors.
Conclusion
As long as the roots of Tourette syndrome remain a mystery, the question of what triggers my own diagnosis and symptoms cannot be fully answered. The disorder is far more complex than I could have ever imagined and the vast quantity of research investigating its origins is equally as convoluted. Although researchers have uncovered anatomical, physiological, genetic, and non-genetic factors, there is still much to understand. One absolute certainty is that Tourette syndrome cannot be attributed to one single element. Though the lack of definitive answers is disheartening, I am happy to have gained a better understanding and appreciation of my disorder.

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