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The Gilles De La Tourette Association in New York, NY is a leading organization dedicated to supporting individuals with Tourette and other Tic Disorders, which affect approximately 1 in every 100 people in the United States. They strive to raise awareness, provide advocacy, and conduct groundbreaking research to improve the lives of those living with tics and Tourette, offering a growing community of support and resources. With a focus on hereditary, childhood-onset, neurodevelopmental conditions, the association aims to address the range of symptoms, from mild to severe, that can significantly impact quality of life. While treatments and medications may be available, the organization recognizes the need for consistent care and effective solutions, as there is currently no cure. By sharing personal stories and promoting understanding, the Gilles De La Tourette Association is at the forefront of changing lives and fostering a sense of community among those affected by tics and Tourette.Generated from the website

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