Tourette Association of America

Tourette Association of America (TAA) is a United States-based organization dedicated to advocating for individuals with Tourette Syndrome (TS) and their families. Founded in 1972, the TAA aims to raise awareness, support research, and provide resources and support to those affected by Tourette Syndrome and the spectrum of tic disorders. The association plays a crucial role in improving the quality of life for individuals with TS through education, advocacy, and the promotion of social acceptance.

History

The Tourette Association of America was established in 1972 by a group of parents passionate about finding support and resources for their children diagnosed with Tourette Syndrome. Since its inception, the TAA has grown significantly, expanding its reach and services to meet the evolving needs of the TS community. The organization has been instrumental in funding research, increasing public awareness, and fostering a supportive community for individuals with TS and their families.

Mission and Vision

The mission of the Tourette Association of America is to make life better for all people affected by Tourette and Tic Disorders. The vision of the TAA is a world where every person affected by TS and related disorders can reach their full potential. To achieve this, the TAA focuses on research, support, education, and advocacy.

Programs and Services

The TAA offers a wide range of programs and services designed to support individuals with TS and their families. These include:

• Education and Awareness: The TAA provides comprehensive resources for individuals, families, educators, and healthcare professionals to increase understanding of Tourette Syndrome. This includes workshops, webinars, and educational materials.

• Support Networks: The organization facilitates a network of support groups across the country, offering a platform for individuals and families to share experiences and receive emotional support.

• Research Funding: The TAA funds research aimed at understanding the causes of TS, developing effective treatments, and ultimately finding a cure. The association collaborates with researchers and institutions worldwide.

• Advocacy: The TAA advocates for public policies and practices that promote the rights and interests of individuals with TS. This includes efforts to improve access to treatments and accommodations in educational settings.

Events

The Tourette Association of America organizes various events throughout the year to raise awareness and funds for TS. These include the National Awareness 5K Run/Walk, the annual Gala, and Tourette Syndrome Awareness Month activities in May.

Membership

Membership in the TAA is open to individuals, families, and professionals interested in supporting the mission and activities of the organization. Members receive benefits such as discounts on TAA events and access to exclusive resources.

See Also

• Tourette Syndrome
• Tic Disorders
• Neurodevelopmental Disorders

External Links

• Official Website of the Tourette Association of America

‎