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The Tourettes Action Blog
The Tourettes Action blog gives people with Tourette Syndrome (TS) a space to talk about how the condition affects them. We hope that by explaining what life is really like to have or to live with someone who has TS, we can fight the stigma about the condition.
If you would like to write about your experiences of TS, we would love to hear from you. Please email us to find out more and discuss what you might like to write about.
The Power of Sport
'It is more than a hobby, it his lifeline, when he finds a sense of control over his body'.
Posted 3hrs ago
Acting With Tourette's
I remember my first experience of acting in front of a camera, I was so nervous that everyone would see my tics and I would be written off as an actor forever. To my surprise, there were no shrugs, flicks or jerks, just me acting my lines; I couldn’t believe it!
Posted Wed 3rd Sep 2025 at 09:00
Living with Tourette’s: My Journey Since 2020
In October 2020, just months after the pandemic had turned all of our lives upside down, I was diagnosed with Tourette syndrome.
Posted Tue 2nd Sep 2025 at 11:15
My Tourette’s and why I want to help you!
My name is Ewan, I run my own business as a Sport’s Therapist, and I have Tourette’s.
Posted Tue 5th Aug 2025 at 11:14
Living with a chronic illness
My name is Missy and I come with accessories. Some are obvious, like my wheelchair, some are hidden, which do you think are the most hard to live with?
Posted Mon 7th Jul 2025 at 09:28
