Tourette Canada

Tourette Canada is a national voluntary organization dedicated to improving the quality of life for those with or affected by Tourette Syndrome (TS) through programs of education, advocacy, support, and the promotion of research. Founded in 1976, the organization has been at the forefront of efforts to increase public awareness of Tourette Syndrome, provide information and resources to individuals and families living with the condition, and advocate for the needs and rights of the TS community in Canada.

History

Tourette Canada was established in 1976 by a group of parents who sought to create a support network for families affected by Tourette Syndrome. Since its inception, the organization has grown significantly, expanding its services and reach across the country. It has played a crucial role in fostering a better understanding of TS among the general public, healthcare professionals, and educators.

Mission and Vision

The mission of Tourette Canada is to help individuals with Tourette Syndrome and their families by providing support, education, and advocacy, and by promoting research into the cause, treatment, and management of TS. The organization envisions a world where people with Tourette Syndrome are accepted and supported in their communities and have access to effective treatments and resources.

Programs and Services

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

• Support Groups: Local chapters and support groups across Canada offer a safe and understanding environment where individuals and families can share experiences and coping strategies.
• Education: The organization provides educational resources and training for individuals, families, educators, and healthcare professionals to promote understanding and effective management of TS.
• Advocacy: Tourette Canada advocates for the rights and needs of individuals with TS, working to ensure access to treatments, accommodations in education and employment, and raising awareness to reduce stigma.
• Research: The organization supports and promotes research into the causes, treatment, and management of Tourette Syndrome, aiming to improve the quality of life for those affected by the condition.

Membership and Volunteering

Tourette Canada offers membership to individuals and families interested in supporting the organization's mission. Members receive updates on the latest TS research, events, and programs. The organization also relies on the dedication of volunteers who contribute their time and skills to support its various initiatives.

Events and Awareness Campaigns

Throughout the year, Tourette Canada organizes events and awareness campaigns to educate the public about Tourette Syndrome and to raise funds for its programs and services. These events provide opportunities for individuals and families to connect, share their stories, and support each other.

See Also

• Tourette Syndrome
• Neurodevelopmental disorder
• Advocacy
• Health education

External Links

• Official Website of Tourette Canada

‎ ‎

---

Translate: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, தமிழ், తెలుగు, Urdu, ಕನ್ನಡ, Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, বাংলা
European español, Deutsch, français, Greek, português do Brasil, polski, română, русский, Nederlands, norsk, svenska, suomi, Italian
Middle Eastern & African عربى, Turkish, Persian, Hebrew, Afrikaans, isiZulu, Kiswahili,
Other Bulgarian, Hungarian, Czech, Swedish, മലയാളം, मराठी, ਪੰਜਾਬੀ, ગુજરાતી, Portuguese, Ukrainian