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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.
Tourette’s without limitations:
Recently, I’ve been given pause for reflection. Over the span of my nearly 30 years on this pale blue dot that we call home, I’ve struggled to come to terms with the impact that my Tourette’s has had on my life.
Posted Thu 11th Jul 2024 at 08:47
Masters research helped increase my understanding of TS stigma and how things need to change
When deciding what to research for my master’s dissertation I knew I wanted to do it about Tourette Syndrome (TS). It has been a subject I’ve done a lot of personal research on over the years in the hopes I could help a family member.
Posted Mon 17th Jun 2024 at 09:55
DBS Brain Op changed my life
Tom Dufton shares his journey to this pioneering treatment
Posted Wed 29th May 2024 at 12:54
Managing Tourette’s in the Workplace
As someone who has been ticcing all her life, I understand the challenges that come with navigating professional environments while trying to manage tics.
Posted Tue 14th May 2024 at 09:53
