REFERENCE · RECOVERY TECHNIQUE
Planning for Intense Bouts and Difficult Days
Original entry 8: Tic-attack, cluster and flare planning.
For the Person With FND
For Family, Friends, and Other Supporters
For Clinicians and the Care Team
Research and Sources
—
For the Person With FND
What the terms mean
A cluster is a period when symptoms occur close together. People sometimes call a particularly intense bout a tic attack. A flare is a spell when the overall symptom burden is greater than usual. These descriptions can help you explain your experience, but they do not by themselves establish the diagnosis. An intense bout is not automatically a functional seizure. [1]
A useful plan works even if there is no warning. It records what a familiar event usually looks like, what help is wanted and which changes need medical assessment.
Agree on help before it is needed
Ask your care team to help write a brief plan. Include who can be contacted, how to make the surroundings safer and how you will communicate if speaking is interrupted. A supporter should know whether you prefer quiet company, more space or a simple check-in.
During a familiar bout, reduce nearby hazards where possible. Put down hot or sharp objects if you can do so safely. Supporters can move objects away without holding you down. Avoid demanding that you stop the movements or testing whether you can suppress them.
If injury occurs, assess it on its own merits. A known functional diagnosis does not make a head injury harmless. Follow individual emergency advice and seek urgent help for serious injury, breathing or swallowing danger, new confusion or a new neurological change. [2]
Afterwards
Allow time to recover and check what is needed before restarting an activity. A short review later may be more useful than detailed questioning while exhausted. You might simply note what help worked and whether something was different.
A flare does not erase progress. Studies of young people show varied courses, including persistent or worsening symptoms for some. Continuing care should remain available when improvement is limited. [3]
Contact your care team if bouts become more frequent, more injurious or different from the agreed pattern. Review pain, sleep, other conditions and whether the current treatment plan is manageable. Do not assume every deterioration needs more practice.
For the Person With FND
For Family, Friends, and Other Supporters
For Clinicians and the Care Team
Research and Sources
—
For Family, Friends, and Other Supporters
Keep your voice calm, reduce an audience where possible and use the agreed communication approach. Calmness is a way of offering care, not a reason to overlook injury or distress.
Do not restrain the person or put objects in their mouth. If you are unsure whether an event is familiar or safe, seek medical help and follow dispatcher advice. Review the plan with the person after recovery, including what you found difficult.
For the Person With FND
For Family, Friends, and Other Supporters
For Clinicians and the Care Team
Research and Sources
—
For Clinicians and the Care Team
Document the event phenotype and differential diagnosis, including primary tic attacks, functional seizures and other episodic events where relevant. Specify individualized escalation criteria without using an arbitrary duration as proof of etiology. Review injury burden, medication effects and coexisting conditions. [1]
The 2025 tertiary adolescent follow-up used parent/carer reports and found varied outcomes. It supports avoiding universal recovery promises; it does not establish the efficacy of a flare plan or predict an individual’s course. [3]
For the Person With FND
For Family, Friends, and Other Supporters
For Clinicians and the Care Team
Research and Sources
—
Research and Sources
This page expands supportive safety and follow-up planning. Head-injury guidance is adjacent safety evidence. The adolescent outcome study is observational and based on a selected service population, not a treatment comparison.
| Citation | Figure | Full citation and scope |
|---|---|---|
| [1] | — | Malaty IA, Anderson S, Bennett SM, et al. Diagnosis and management of functional tic-like phenomena. Journal of Clinical Medicine. 2022;11(21):6470. Source. FND-CIT-0110. |
| [2] | — | NHS. Head injury and concussion. Reviewed May 29, 2025; accessed September 24, 2026. Source. FND-CIT-0217. |
| [3] | — | Ducroizet A, Eccles C, Lancaster R, et al. Outcomes of functional tics in adolescents: a single-centre tertiary study. Archives of Disease in Childhood. 2025;110(7):528–532. Source. Parent/carer interviews concerning 43 adolescents; selected service population and reported outcomes limit generalization. FND-CIT-0219. |
Evidence checked September 24, 2026. Human review pending. No new community quotations have been verified.
For the Person With FND
For Family, Friends, and Other Supporters
For Clinicians and the Care Team
Research and Sources
—