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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.
I Don't Have Tourettes!
Rachel Miles, mum to 8 year old Shae, tells us how TicFest South was a life-changing weekend for her family.
Posted Thu 13th Jul 2017 at 12:00
Reclaiming the T-word
Tourettes Action Research Manager, Dr Seonaid Anderson highlights the systemic misuse of the word 'tourettes' and how this continues to compound the stigma surrounding the condition.
Posted Wed 5th Jul 2017 at 10:30
Research left me feeling awesome and unique!
Clair Beckett gives her account of being a research participant for a study looking at 'attentional and inhibitory mechanisms in Tourette syndrome.'
Posted Mon 3rd Jul 2017 at 11:09
What it feels like to have Tourette Syndrome
11 year old Romy talks about living with TS
Posted Mon 19th Jun 2017 at 11:52
Insightful answers to interesting question from regular blogger Adrian Reynolds
Adrian lifts the lid on questions that he has been asked by friends and strangers about living with TS.
Posted Tue 13th Jun 2017 at 12:41
