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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.
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
You're not the only one!
What happens when you have your life vaguely planned out, but then wake up one day with Tourettes?
Posted Mon 19th Apr 2021 at 13:15
How deep pressure helped me control my Tourette Syndrome
Ellen Adby shares her experience of using a weighted blanket to help with tics.
Posted Tue 19th Jan 2021 at 14:43
How TS paved the way to my career as a professional Beatboxer
My name is Dean Yhnell, I’m 36 and I make weird noises. I now in fact make noises for a living. I have Tourette Syndrome and I’d like to tell you all how Beatboxing has positively made me who I am today.
Posted Wed 2nd Dec 2020 at 13:00
