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Tourette's Syndrome and Tic Disorders

Understanding Tourette's Syndrome and Tic Disorders — what it is, the signs people notice, and where to find support. Educational, not a diagnosis.

By the Emotionally Me team · Last updated: 17 July 2026

What is Tourette's Syndrome and tic disorders?

Tourette's Syndrome is a neurological condition involving tics — sudden, repeated movements or sounds that a person makes involuntarily. To be called Tourette's, someone has both movement (motor) and sound (vocal) tics that have lasted more than a year; other tic disorders may involve just one type or a shorter period. Tics usually begin in childhood and often ease in adulthood. It's a difference in how the brain works, a form of neurodivergence, not an illness to be ashamed of, and it isn't linked to intelligence. Many people with Tourette's are creative, quick-thinking, funny, resilient and highly empathetic, having navigated a world that doesn't always understand them.

What are the common signs / experiences of Tourette's and tic disorders?

Tics vary widely and change over time. Motor tics can be simple (blinking, head jerks, shrugging) or more complex (touching, jumping). Vocal tics can be simple (throat-clearing, sniffing, grunting) or more complex (repeating words or phrases). Many people feel a building urge or sensation just before a tic — a bit like needing to sneeze — and a release afterwards. Tics can be worse with stress, excitement or tiredness, and can sometimes be held back briefly, though that takes effort and can be exhausting. Tics come and go and shift in type. Tourette's often occurs alongside things like ADHD, OCD or anxiety, and everyone's experience is genuinely their own.

How do I know if I might have Tourette's or a tic disorder?

You might wonder about it if you've had repeated, involuntary movements or sounds — perhaps since childhood — often with that tell-tale urge or tension beforehand and relief afterwards. Maybe they change over time, or flare with stress or excitement. Recognising this in yourself is a valid and understandable first step, but it is not a diagnosis. Tics can have several causes, and only a professional can assess them properly. If tics are affecting your daily life or wellbeing, it's worth talking to your GP, who can refer you on. Getting understanding and, if needed, an assessment can bring real reassurance — you don't have to guess alone.

What causes Tourette's and tic disorders?

The exact cause isn't fully understood, but Tourette's is thought to involve differences in parts of the brain that help regulate movement, and in the brain's chemical messengers. It tends to run in families, so genetics play a part, and it often appears alongside conditions like ADHD or OCD. It's something a person is born predisposed to, not something caused by upbringing, diet, 'bad behaviour' or a lack of self-control. Tics are involuntary — not deliberate and not a habit someone can simply choose to stop. There's nothing anyone did to cause Tourette's, and nothing about it that reflects a person's character or effort.

Does Tourette's mean swearing uncontrollably?

No — this is the biggest myth about Tourette's, and it's worth busting clearly. Involuntary swearing (called coprolalia) affects only a small minority of people with Tourette's — roughly 1 in 10 — yet it's what films and headlines fixate on. Most people with Tourette's never swear involuntarily at all. Their tics are far more likely to be things like blinking, head movements, throat-clearing or sniffing. Reducing Tourette's to 'the swearing condition' is inaccurate and can be hurtful and isolating for the many people it doesn't fit. Tourette's is a varied neurological condition about tics in general — not about swearing — and understanding that helps replace stigma with acceptance.

How is Tourette's diagnosed/assessed?

In the UK, Tourette's is diagnosed by a health professional — usually via a GP referral to a specialist such as a neurologist or paediatrician. There's no single blood test or scan; instead, the specialist takes a careful history of the tics: what they are, how long they've lasted (both motor and vocal tics for over a year for Tourette's), and how they affect daily life, while ruling out other causes. For a child, the GP or school can help start this process. It's not something to self-diagnose. A proper assessment brings clarity, helps make sense of any related conditions, and opens the door to understanding and support where it's wanted.

What support or adjustments help?

The aim is support and understanding, not 'curing' who someone is — and many people don't need or want treatment at all. When tics are distressing or disruptive, behavioural therapies such as habit-reversal or comprehensive behavioural intervention for tics (CBIT) can help someone manage the urge. Reducing stress, resting well, and calm, accepting environments all tend to ease tics. In school or work, reasonable adjustments (a legal right in the UK) might include a tolerant setting, movement breaks, extra time, or a quiet space. Sometimes medication is considered for significant tics. Most powerful of all is acceptance — letting people tic without judgement so they don't have to spend exhausting energy holding it in.

How can I support myself or someone I love who has Tourette's?

The kindest thing is acceptance: try not to draw attention to tics, tell someone to 'stop', or stare — tics are involuntary, and suppressing them is tiring. Stay calm and patient, especially during a flare, and remember stress and excitement can make tics stronger, so a relaxed atmosphere really helps. Focus on the whole person and their strengths, not the tics. Learn the facts, and gently challenge myths like the swearing stereotype when you hear them. If it's you, be compassionate with yourself and rest when you need to. Above all, make sure the person feels safe, understood and valued exactly as they are — that acceptance changes everything.

Where can I get help right now?

A great UK starting point is Tourettes Action, which offers information, support and resources for people with Tourette's and tic disorders, and their families. Your GP is the route to assessment and can refer you to specialist services if needed, and for children the school can help too. Connecting with others who understand can be reassuring and reduce isolation. If you are struggling emotionally and need urgent support with how you're feeling right now, please see the support box at the top of this sheet. Reaching out is a positive step — there are people and organisations who understand Tourette's and genuinely want to help.

Sources & further reading

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