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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.
How have noise cancelling headphones helped me as a multiple disabled person?
Oliver shares how a TA grant allowed him to purchase a vital piece of equipment.
Posted Tue 21st Feb 2023 at 10:03
'I’ve had more questions than a TV gameshow about my condition!'
23 year old NHS Health and Fitness practitioner, Lewis, shares his personal story.
Posted Mon 13th Feb 2023 at 09:31
New TS video game 'Tourettes Simulator'
Game developer creates a fun, interactive game to spread awareness of TS
Posted Wed 25th Jan 2023 at 11:28
TS Champion Saphia Baktout
14 year old Saphia shares her holiday experience with us, and how a negative can be turned in to a positive.
Posted Mon 23rd Jan 2023 at 14:49
