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Cerebral Palsy information card
⚡ Neurological

Cerebral Palsy

A group of lifelong disorders affecting movement and posture due to a non-progressive disturbance in the developing brain. Needs and abilities vary widely.

🧸 Early Years 🏫 School Age 🧑 Teens & Adults ♾️ Lifelong
Information quality and medical scope This page is general information, not a diagnosis or individual medical advice. Symptoms, diagnostic criteria and treatment evidence can change over time, and people can present very differently. Database record last updated: 25 August 2026. See how Awareverse reviews condition information.

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📖 Overview

Cerebral palsy (CP) is the most common physical disability in childhood. It is caused by damage to or differences in the developing brain, usually before, during, or shortly after birth. The brain damage is non-progressive — it does not get worse over time — but the effects on the body change as the person grows.

CP affects movement, muscle tone, and coordination. Every person with CP is different — the type, distribution, and severity of motor involvement varies enormously, as do intelligence, communication, and associated conditions.

TYPES OF CEREBRAL PALSY

Spastic Cerebral Palsy
The most common type, affecting approximately 80% of people with CP. Spasticity means increased muscle tone — the muscles are stiff or tight, making movement difficult and sometimes painful. Spastic CP is further described by which parts of the body are affected:
Spastic hemiplegia — one side of the body affected (arm and leg on the same side). Often the arm is more affected than the leg. Many people with hemiplegia walk independently but may have significant hand function difficulties.
Spastic diplegia — both legs primarily affected, with the arms less involved or unaffected. Common in premature babies. Many people with diplegia walk, sometimes with aids.
Spastic quadriplegia — all four limbs affected, usually severely. Often the most complex form, frequently involving speech, swallowing, and cognitive difficulties as well as motor.

Dyskinetic Cerebral Palsy
Dyskinetic CP involves involuntary, uncontrolled movements — writhing (athetosis), twisting (dystonia), or abrupt jerking (chorea). The muscle tone fluctuates, changing from floppy to stiff. Speech and facial movements are often significantly affected. Cognitive ability cannot be inferred from the severity of motor or speech impairment. Some people with dyskinetic CP have typical intellectual ability while others have intellectual disability, so accessible assessment and communication are essential.

Ataxic Cerebral Palsy
Ataxic CP affects balance and coordination. Movements are shaky and unsteady — the person has difficulty with tasks requiring precision, balance, and coordination. Walking may be broad-based and unsteady. The least common type of CP.

Mixed Cerebral Palsy
Many people have features of more than one type — most commonly spasticity with dystonia. Mixed CP is common in more severely affected individuals.

GROSS MOTOR FUNCTION CLASSIFICATION SYSTEM (GMFCS)
The GMFCS classifies CP from Level I (walks without limitations) to Level V (transported in a manual wheelchair, very limited self-mobility). This classification gives a better picture of functional ability than type alone.

ASSOCIATED CONDITIONS
CP is a motor condition but is frequently accompanied by: epilepsy and intellectual disability (both common, with rates varying by CP type, severity and study), speech and communication difficulties, vision impairment, hearing impairment, pain (particularly in adulthood), eating and swallowing difficulties (dysphagia), bladder and bowel difficulties, and mental health difficulties.

Pain is common in cerebral palsy and can arise from muscle tone, joints, positioning, procedures or unrelated health problems. Pain should be assessed directly and not assumed to be an unavoidable part of CP.

ADULTHOOD
The brain disturbance causing CP is non-progressive, but symptoms, pain, mobility and functional ability can change across the lifespan. Musculoskeletal complications, fatigue, ageing and access to healthcare can all affect adult function. Changes should be assessed rather than assumed to be inevitable deterioration.

COMMUNICATION IN CEREBRAL PALSY
Speech is affected in many people with CP — either by the motor involvement of the muscles used for speech, or by associated communication difficulties. Unclear speech does not reflect intelligence. AAC is used by many people with CP and should be resourced and supported throughout life.

Eye-gaze systems can provide communication access for some people who cannot reliably use speech or their hands. Suitability and accuracy depend on vision, motor control, cognition, positioning, calibration and individual assessment.

🔍 Key Characteristics

Movement coordination difficulties
Muscle tone differences tight loose fluctuating
May affect walking hand use speech
Involuntary movements or tremors
Associated conditions epilepsy learning disabilities
Fatigue from extra movement effort
Speech may be affected dysarthria
Intelligence often unaffected wrongly assumed

🌅 What Day to Day Life Can Look Like

Physical tasks take more time and energy — dressing, eating, moving between places
Fatigue is significant — movement requires more effort than for non-disabled peers
Pain is common, particularly in joints and muscles, and often increases with age
Communication may be affected — speech may be unclear, AAC may be used
Getting around — stairs, uneven surfaces, distance — requires planning and often assistance
Spasms, involuntary movements, or muscle tightness may worsen with fatigue, temperature, or illness
Epilepsy and other associated conditions need ongoing management
Equipment — wheelchair, orthotic splints, communication aids — is part of daily life
Healthcare appointments are frequent — physio, OT, orthopaedics, neurology
People underestimate cognitive ability based on physical presentation — this is isolating and frustrating

❌ What People Often Get Wrong

Cerebral palsy does not automatically imply intellectual disability; cognition should be assessed accessibly and separately from movement or speech
Unclear or absent speech does not establish a person’s understanding; AAC and accessible assessment may reveal abilities that speech cannot show
CP results from a disturbance in the developing brain and is not usually something a parent caused
The original brain disturbance is non-progressive, but pain, musculoskeletal problems, fatigue and functional ability can change across life
Wheelchairs, walkers and other mobility aids can increase participation and conserve energy rather than representing failure
Independence varies widely; good support should maximise choice, access and participation rather than assume one outcome
Pain and fatigue are common in many adults with CP and deserve assessment for treatable contributors
People with CP have the same rights to relationships, education, work and self-determination as other people

✅ What Helps

Accessible assessment of communication, cognition, movement, pain and participation
Physiotherapy, occupational therapy, speech and language therapy or rehabilitation according to individual goals
AAC and assistive technology when speech does not provide reliable communication
Mobility aids, orthoses, seating and positioning equipment when clinically useful
Pain, tone, hip, spine, sleep and other health monitoring according to the person’s CP profile
Energy conservation, rest or activity adaptation when fatigue limits participation
Do not infer cognitive ability from movement, facial expression or speech clarity
Support strategies are general examples, not treatment instructions. Medication, therapy and clinical decisions should be discussed with an appropriately qualified professional.

🏫 School & Education Support

Physical accessibility — ramps, lifts, adapted toilet, appropriate seating and desk height
AAC device training for staff and integration into the school day if used
Extra time in all written tasks — fine motor difficulties affect writing speed
Adapted PE with meaningful participation at the right level
Physiotherapy programme integrated into the school day where needed
Healthcare care plan for any medical needs — epilepsy, medication, tube feeding
Fatigue management — rest breaks, reduced physical demands at key times
Personal care support provided with dignity and privacy
Transition planning to later secondary or postsecondary well in advance
Assumptions about cognitive ability based on physical presentation must be actively challenged by staff

⚠️ Safety & Red Flags

Pain that is not being adequately assessed or managed — very common and very serious
Swallowing difficulties — aspiration pneumonia risk if not managed
Seizure activity changing or worsening
Equipment failure or needs not met — wheelchair breakdown, AAC device not working
Safeguarding concerns — people with CP are at higher risk of abuse, particularly if communication is limited
Scoliosis developing or worsening
Transition to adult services breaking down — a high-risk period
Increasing isolation as physical barriers to participation grow
Mental health difficulties developing alongside physical condition
Any placement that does not have the physical accessibility and trained support the person needs
Check current clinical guidance. Awareverse aims to separate established evidence, practical support ideas and lived experience. If a statement here conflicts with current NHS, NICE or another relevant clinical authority, use the current professional guidance and tell us so we can review the page. Read the review policy.

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