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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.
My own diagnostic journey has inspired me to pursue a PhD
Danni Phoenix-Kane shares her journey seeking an adult TS diagnosis, the support she received from organisations such as Tourettes Action and her future aspirations to research and advocate for the Adult TS community.
Posted Tue 11th May 2021 at 10:00
How Tourette Syndrome made me the man I am today
"It's all about how you see yourself, not how others see you".
Posted Wed 5th May 2021 at 12:13
Duke of Edinburgh Blog
For the volunteering element of his DofE bronze award, 14 year old Noah will be writing a weekly blog for 12 weeks
Posted Tue 4th May 2021 at 14:55
A late Diagnosis
Hi, my name’s Rob, I’m 52 and I was diagnosed with Tourette Syndrome in 2020.
Posted Wed 28th Apr 2021 at 12:44
‘We might not be able to cure Tourettes but we can cure ignorance.’ Anonymous.
12 year old Erin talks about her experience of moving from primary to secondary school
Posted Mon 19th Apr 2021 at 13:25