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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.


  • 19 year old Amber talks about school, employment and finding her confidence.

    Growing up my family and teacher would always tell me off for making funny noises or pulling a face and I just couldn't understand why I was being yelled at.

    Posted Thu 24th Nov 2016 at 14:07
    by Amber

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  • Spencer Martin aged 13 and 3/4

    13 year old Spencer talks about being a teenager with TS and how proud he is of his inspirational mum.

    Posted Wed 23rd Nov 2016 at 11:48
    by Spencer Martin

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  • Adolescents Perception of their Peers with Tourette Syndrome: An Exploratory study

    Melina Malli is a PhD researcher at the Tizard Centre in the University of Kent. She has also worked with people with TS as a special educational teacher. With her supervisor Professor Rachel Forrester-Jones they aim to develop an intervention to improve tic-free teenagers' attitudes towards their peers with TS. In order to achieve that, they needed to investigate what teenagers without TS thought about their peers with TS and how they believed they would behave and act around them. Their finding, taken from 22 participants without TS, provides insight into what an effective intervention should have in order to improve school experience for those with TS.

    Posted Mon 21st Nov 2016 at 13:17
    by Melina Malli

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  • The Importance of Peer Support

    Tracey Francis is a freelance writer and researcher with a particular interest in improving the chances and life choices available to young people who face barriers to inclusion. She was awarded a Travel Fellowship by the Winston Churchill Memorial Trust to explore the experiences of young people with Tourettes, Asperger’s Syndrome or ADHD in Italy, Norway and the Czech Republic after they leave school. Her findings, taken from conversations with 50 young people and/or their family members, are the basis of a new report offering practical insights and recommendations to improve the experiences of this group as they make the transition to adulthood. For full details of the project, or to download a copy of the final report, visit www.lifeontheedgeofthecliff.com

    Posted Thu 20th Oct 2016 at 13:28
    by Tracey Francis

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  • Anatomically Speaking - Adrian Reynolds tells us about his tics.

    I have been asked many times exactly what Tourette’s does to me, how it manifests day to day. There is such a frequent shift in severity, frequency, movements and physical toll that it’s of limited value to produce a simple list.

    Posted Thu 6th Oct 2016 at 11:48
    by Adrian Reynolds

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Events

Wednesday 27 November 19:00

Adults with TS Support group, Online 7pm - 8pm

Thursday 28 November 10:00

Parent/Caregiver Online Coffee Morning, Online 10am - 11am

Friday 29 November 10:00

Q&A Drop-in session, Online 10am - 11am

Contact us

If you have any questions we would love to hear from you

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