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Tourette Canada

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Brampton, ON
Tourette Canada

Tourette Canada is a registered (11926 7862 RR0001) charitable organization dedicated to improving the lives of Canadians affected by Tourette Syndrome

08/20/2026

Heading back to school with a child who has Tourette syndrome or OCD? An IPP (or IEP) may be a useful tool for helping them thrive in the classroom.

This webinar from the Tourette OCD Alberta Network breaks down what an IPP is and how parents and educators can work together to build one that meets the student’s needs.

Whether you're a parent advocating for your child or a teacher supporting one, this is a practical place to start.

Watch the full recording 👇
https://www.youtube.com/watch?v=S4kABY_oiUY .

08/17/2026

Summer's winding down. However these past couple of months went for your family (easy stretches, hard ones, or a bit of both), we'd love to hear from you.

If there was something that helped, even a small thing, would you share it? A change in routine. A place your child felt comfortable. A person who made things easier just by being kind about it.

And if this summer was mostly about getting through, that's okay too. Not every season is a good one, and there's no version of this you're supposed to be having.

Whatever you feel comfortable sharing may help another family feel less alone as we head toward September.

08/13/2026

Tourette syndrome was first formally named 140 years ago, but tics are much older.

In 1825, a French doctor named Jean Marc Gaspard Itard documented the case of the Marquise de Dampierre, a French noblewoman with involuntary movements and sounds. This description is widely considered the first formal medical description.

Sixty years later, physician Jean-Martin Charcot set his intern, Georges Gilles de la Tourette, to study patients with movement disorders at a Paris hospital. In 1885, Gilles de la Tourette published an account of nine patients and argued that they had a distinct condition.

Charcot named the condition after Gilles de la Tourette, highlighting his contribution. �
Although the condition already existed, it finally got a name in 1885.

08/07/2026

"Can't you just stop?"

Almost every person with Tourette syndrome has heard it. From a coach. A teacher. A parent who loves them and doesn't know what else to say.

The instinct is understandable. Tics look like something a person is doing, so it seems like something they could undo. But suppressing a tic isn't stopping it; it's holding a sneeze. It builds. And a child who is asked to hold it all day, every day, learns something far more lasting than tic control: They may start to feel their tics are something they need to hide or change.

Those feelings can have a lasting impact. While some adults with Tourette syndrome have their most severe symptoms fade with age, many tell us that the shame can stick around.

So if there's a child in your life with Tourette syndrome, the most useful thing you can give them isn't a strategy for stopping. It's language for what's happening, and the steady support that tells them their tics are nothing to be ashamed of.

Tourette Canada is here to help families with both. Drawing on current research and the lived experience of our own community, we’re here to provide the support, understanding, and knowledge needed to thrive without shame.

08/04/2026

Travelling with someone who has Tourette Syndrome?

Our new guide is for people with TS and the parents, partners, and friends riding along, with simple, matter-of-fact advice that makes the whole trip easier for everyone.

"The road is wide, and there's room on it for everyone."

https://tourette.ca/2026/06/road-trip-ready-a-survival-guide-for-travelling-with-tourette-syndrome/

07/30/2026

"Most people don't know about Tourette's, and that's not good."

That's Evie, 10, who plays drums in a marching band in Northern Ireland and who decided this summer that she wanted to talk publicly about living with Tourette syndrome.

Big crowds and noise can be overwhelming for her. So her band made room for it. If she needs to step out, they work around it. Her mum Christina says other parents have been reaching out since Evie shared her story.

Evie's out there doing the thing she loves, with her mum, her sisters, her aunt, and her granda beside her, using it to help people understand a condition most still get wrong.

That's advocacy. She's ten.

Read her story on BBC News: "Meet the next generation taking part in the Twelfth"

07/23/2026

Did you know Tourette Canada has an online store? Whether you're looking to learn more about Tourette Syndrome or show your support, our store has something for you!

Educational resources like our Understanding Tourette Syndrome Handbook and Tourette Syndrome Q&A Pamphlets are perfect for families, educators, employers, and anyone wanting to better understand TS.

You can also find Tourette Canada apparel and accessories, including: T-shirts, Mitts, Toques and Face masks.

Every purchase helps support Tourette Canada's mission of providing education, advocacy, and support to Canadians living with Tourette Syndrome and its associated conditions.

Whether you're raising awareness, starting conversations, or simply looking for trusted resources, we've got you covered.

07/22/2026

Packing for a road trip with Tourette Syndrome? A few things worth tossing in the bag: extra medication in labelled containers, a brief written summary of your diagnosis, noise-cancelling headphones, and a familiar comfort item or two.

We've pulled together a full survival guide: what to plan before you leave, how to handle the sensory chaos of the car, and how to settle in once you arrive.

https://tourette.ca/2026/06/road-trip-ready-a-survival-guide-for-travelling-with-tourette-syndrome/

07/17/2026

We're Tourette Canada: a nationally registered, volunteer-based charity dedicated to improving the lives of Canadians living with Tourette Syndrome (TS) and its associated conditions.

Behind everything we do is an incredible community:
💙 Volunteers from coast to coast
💙 A passionate and diverse Board of Directors
💙 Professional advisors sharing their expertise
💙 A small but dedicated staff supporting our national mission

Together, we provide education, advocacy, support, and programs that help individuals, families, educators, healthcare professionals, and communities better understand Tourette Syndrome.

You may have noticed the kite in our logo. It represents every person living with TS. Like a kite in the wind, each journey is unique. There are moments of challenge and moments of triumph. With understanding, support, and the right resources, those turbulent winds can become the lift that helps each person soar.

Whether you've been part of our community for years or you've only just found us: welcome. We're glad you're here. 💙

07/13/2026

If you're just starting your journey with Tourette Syndrome, this one's for you.

This comprehensive webinar recording from the Tourette OCD Alberta Network walks parents through "How to Talk to Your Kids About Tics"

Presented by Dr. Jen Ference-Belhomme, a registered psychologist, and a mom of three, whose oldest child's Tourette diagnosis deeply shapes both her work and her perspective.

As Dr. Ference-Belhomme says in the webinar, every parent has that moment when they wish their kid came with a manual. Not to fix anything but to make sure they're making good choices.

"Am I asking the right questions?"
"Am I helping?"

This webinar meets you right there, with a key reminder that connection comes first: building, maintaining, and repairing connection with our kids matters most.

Plus, Dr. Ference-Belhomme shares some great resources to take with you.

Watch the full recording: https://www.youtube.com/watch?v=Bgsz8rQgvrU

Address

5 Nevets Road
Brampton, ON
L6T5T2

Opening Hours

Monday	9am - 4:30pm
Tuesday	9am - 4:30pm
Wednesday	9am - 4:30pm
Thursday	9am - 4:30pm

Telephone

+18003613120

Website

https://tourettecanada.akaraisin.com/ui/donate/donations/start

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