Are there support groups for Tourettes?

The Southern California Chapter has six support groups throughout the region. These groups meet several times per year and provide an excellent chance for families or individuals to spend time together, share experiences, and learn more about TS.

What specialist deals with Tourettes?

If you or your child has been diagnosed with Tourette syndrome, you may be referred to specialists, such as:

• Doctors who specialize in brain disorders (neurologists)
• Psychiatrists or psychologists.

Is Tourettes a Recognised disability?

Tourette Syndrome may be recognised as a disability according to the definition of disability under the Equality Act 2010; this will depend on the severity of your condition and how it impacts your life.

How do I calm my tics?

There are some simple things you can do that may help to improve your or your child’s tics.

1. avoid stress, anxiety and boredom – for example, try to find a relaxing and enjoyable activity to do (such as sport or a hobby).
2. avoid becoming too tired – try to get a good night’s sleep whenever possible.

Where can I find local support for Tourette syndrome?

Our Chapters and Support Groups provide local support across the nation for families, individuals, and adults with Tourette Syndrome and Tic Disorders and the professionals who serve them. There are currently no Chapters in this selected state. If you’d like to learn how to get involved please contact the Tourette Association 888-4TOURET!

Where can I find the Tourette Association of America?

Browse listing and locations near you. Browse featured tool kits and resources that are designed to support children, young adults, educators, law enforcement, care givers, patients and families and more! Click here if you are interested in being included on the Tourette Association’s Physician & allied Professionals Referral List.

How does njcts help people with Tourette syndrome?

NJCTS provides answers for these individuals and their families through referrals to programs and services, education and training so that families, peers and professionals will be better qualified to help those with TS, and support of research programs so that we can find better treatments and a cure.

What do you need to know about Tourette syndrome?

NJCTS Holds all kinds of events, from seminars to walkathons to summer camps. Your generous support is key to making advances in Tourette Syndrome research and helping keep our ongoing services possible. We are always in need of teens, adults, and families to help spread the word, get some office work done, or help out at an event.